J. R. Alaro, A. Partridge, K. Miura, A. Diouf, A. M. Lopez et al., A chimeric Plasmodium falciparum merozoite surface protein vaccine induces high titers of parasite growth inhibitory antibodies, Infect. Immun, vol.81, pp.3843-3854, 2013.
DOI : 10.1128/iai.00522-13
URL : https://iai.asm.org/content/81/10/3843.full.pdf

A. S. Aly, M. J. Downie, C. B. Mamoun, and S. H. Kappe, Subpatent infection with nucleoside transporter 1-deicient Plasmodium blood stage parasites confers sterile protection against lethal malaria in mice, Cell. Microbiol, vol.12, pp.930-938, 2010.
DOI : 10.1111/j.1462-5822.2010.01441.x
URL : https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1462-5822.2010.01441.x

B. E. Barton, IL-6: insights into novel biological activities, Clin. Immunol. Immunopathol, vol.85, pp.16-20, 1997.
DOI : 10.1006/clin.1997.4420

W. Beghdadi, A. Porcherie, B. S. Schneider, D. Dubayle, R. Peronet et al., Inhibition of histamine-mediated signaling confers signiicant protection against severe malaria in mouse models of disease, J. Exp. Med, vol.205, pp.395-408, 2008.

J. Bhisutthibhan, M. A. Philbert, H. Fujioka, M. Aikawa, and S. R. Meshnick, The Plasmodium falciparum translationally controlled tumor protein: subcellular localization and calcium binding, Eur. J. Cell Biol, vol.78, pp.80052-80053, 1999.
DOI : 10.1016/s0171-9335(99)80052-1

M. Bodescot, O. Silvie, A. Siau, P. Refour, P. Pino et al., Transcription status of vaccine candidate genes of Plasmodium falciparum during the hepatic phase of its life cycle, Parasitol. Res, vol.92, pp.449-452, 2004.

C. J. Janse, J. Ramesar, and A. P. Waters, High-eiciency transfection and drug selection of genetically transformed blood stages of the rodent malaria parasite Plasmodium berghei, Nat. Protoc, vol.1, pp.346-356, 2006.

S. Jung, D. Unutmaz, P. Wong, G. Sano, K. De-los-santos et al., In vivo depletion of CD11c + dendritic cells abrogates priming of CD8 + T cells by exogenous cellassociated antigens, Immunity, vol.17, pp.365-370, 2002.

T. Kishimoto, S. Akira, and T. Taga, Interleukin-6 and its receptor: a paradigm for cytokines, Science, vol.258, pp.593-597, 1992.

C. Mathieu, C. Demarta-gatsi, A. Porcherie, S. Brega, S. Thiberge et al., Plasmodium berghei histamine-releasing factor favours liver-stage development via inhibition of IL-6 production and associates with a severe outcome of disease, Cell. Microbiol, vol.17, pp.542-558, 2015.

T. Miyagami, I. Igarshi, and M. Suzuki, Plasmodium berghei: long lasting immunity induced by a permanent attenuated mutant, Zentralbl. Bakteriol. Mikrobiol. Hyg, vol.264, pp.502-512, 1987.

F. M. Ndungu, E. T. Cadman, J. Coulcher, E. Nduati, E. Couper et al., Functional memory B cells and long-lived plasma cells are generated after a single Plasmodium chabaudi infection in mice, PLoS Pathog, vol.5, p.1000690, 2009.

F. Nimmerjahn and J. V. Ravetch, Divergent immunoglobulin g subclass activity through selective Fc receptor binding, Science, vol.310, pp.1510-1512, 2005.

S. Pied, L. Rénia, A. Nüssler, F. Miltgen, and D. Mazier, Inhibitory activity of IL-6 on malaria hepatic stages, Parasite Immunol, vol.13, pp.211-217, 1991.

D. J. Pombo, G. Lawrence, C. Hirunpetcharat, C. Rzepczyk, M. Bryden et al., Immunity to malaria after administration of ultra-low doses of red cells infected with Plasmodium falciparum, Lancet, vol.360, issue.02, pp.9784-9786, 2002.

I. Puga, M. Cols, C. M. Barra, B. He, L. Cassis et al., B cell-helper neutrophils stimulate the diversiication and production of immunoglobulin in the marginal zone of the spleen, Nat. Immunol, vol.13, pp.170-180, 2012.

E. D. Putrianti, A. Schmidt-christensen, I. Arnold, V. T. Heussler, K. Matuschewski et al., The Plasmodium serine-type SERA proteases display distinct expression patterns and non-essential in vivo roles during life cycle progression of the malaria parasite, Cell. Microbiol, vol.12, pp.725-739, 2010.

R. Spaccapelo, C. J. Janse, S. Caterbi, B. Franke-fayard, J. A. Bonilla et al., Plasmepsin 4-deicient Plasmodium berghei are virulence attenuated and induce protective immunity against experimental malaria. A m, J. Pathol, vol.176, pp.205-217, 2010.

R. Spaccapelo, E. Aime, S. Caterbi, P. Arcidiacono, B. Capuccini et al., Disruption of plasmepsin-4 and merozoites surface protein-7 genes in Plasmodium berghei induces combined virulence-attenuated phenotype, Sci. Rep, vol.1, p.39, 2011.

L. M. Ting, M. Gissot, A. Coppi, P. Sinnis, and K. Kim, Attenuated Plasmodium yoelii lacking purine nucleoside phosphorylase confer protective immunity, Nat. Med, vol.14, pp.954-958, 2008.

S. Waki, J. Tamura, M. Imanaka, S. Ishikawa, and M. Suzuki, Plasmodium berghei: isolation and maintenance of an irradiation attenuated strain in the nude mouse, Exp. Parasitol, vol.53, issue.82, pp.90076-90081, 1982.

M. N. Wykes, Y. H. Zhou, X. Q. Liu, and M. F. Good, Plasmodium yoelii can ablate vaccine-induced long-term protection in mice, J. Immunol, vol.175, pp.2510-2516, 2005.

S. Abdalla, D. J. Weatherall, S. N. Wickramasinghe, and M. Hughes, The anaemia of P. falciparum malaria, British journal of haematology, vol.46, pp.171-183, 1980.

K. Adachi, H. Tsutsui, S. Kashiwamura, E. Seki, H. Nakano et al., Plasmodium berghei infection in mice induces liver injury by an IL-12-and toll-like receptor/myeloid differentiation factor 88dependent mechanism, Journal of immunology, vol.167, pp.5928-5934, 1950.

A. Afonso, P. Hunt, S. Cheesman, A. C. Alves, C. V. Cunha et al., Malaria parasites can develop stable resistance to artemisinin but lack mutations in candidate genes atp6 (encoding the sarcoplasmic and endoplasmic reticulum Ca2+ ATPase), tctp, mdr1, and cg10, Antimicrobial agents and chemotherapy, vol.50, pp.480-489, 2006.

A. A. Aggrey, K. Srivastava, S. Ture, D. J. Field, and C. N. Morrell, Platelet induction of the acute-phase response is protective in murine experimental cerebral malaria, Journal of immunology, vol.190, pp.4685-4691, 1950.

S. T. Agnandji, B. Lell, J. F. Fernandes, B. P. Abossolo, B. G. Methogo et al.,

S. Aponte, S. Machevo, H. Acacio, B. Bulo, E. Sigauque et al.,

C. Theander, D. Drakeley, T. Ansong, S. Agbenyega, H. O. Adjei et al.,

J. Ballou, Y. Cohen, E. Guerra, D. Jongert, A. Lapierre et al., A phase 3 trial of RTS,S/AS01 malaria vaccine in African infants, The New England journal of medicine, vol.367, pp.2284-2295, 2012.

S. T. Agnandji, B. Lell, S. S. Soulanoudjingar, J. F. Fernandes, B. P. Abossolo et al.,

D. Carter, C. Leboulleux, A. Loucq, B. Radford, D. Savarese et al., First results of phase 3 trial of RTS,S/AS01 malaria vaccine in African children, The New England journal of medicine, vol.365, pp.1863-1875, 2011.

M. Aidoo and V. Udhayakumar, Field studies of cytotoxic T lymphocytes in malaria infections: implications for malaria vaccine development. Parasitology today, vol.16, pp.50-56, 2000.

N. E. Alger and J. Harant, Plasmodium berghei: heat-treated sporozoite vaccination of mice, Experimental parasitology, vol.40, pp.261-268, 1976.

J. C. Aliberti, M. A. Cardoso, G. A. Martins, R. T. Gazzinelli, L. Q. Vieira et al., Interleukin-12 mediates resistance to Trypanosoma cruzi in mice and is produced by murine macrophages in response to live trypomastigotes, Infection and immunity, vol.64, pp.1961-1967, 1996.

A. S. Aly, M. J. Downie, C. B. Mamoun, and S. H. Kappe, Subpatent infection with nucleoside transporter 1-deficient Plasmodium blood stage parasites confers sterile protection against lethal malaria in mice, Cellular microbiology, vol.12, pp.930-938, 2010.

A. S. Aly, A. M. Vaughan, and S. H. Kappe, Malaria parasite development in the mosquito and infection of the mammalian host, Annual review of microbiology, vol.63, pp.195-221, 2009.

R. Amino, S. Thiberge, B. Martin, S. Celli, S. Shorte et al., Quantitative imaging of Plasmodium transmission from mosquito to mammal, Nature medicine, vol.12, pp.220-224, 2006.

R. Amson, S. Pece, A. Lespagnol, R. Vyas, G. Mazzarol et al., Reciprocal repression between P53 and TCTP, Nature medicine, vol.18, pp.91-99, 2012.

N. Amzallag, B. J. Passer, D. Allanic, E. Segura, C. Thery et al., TSAP6 facilitates the secretion of translationally controlled tumor protein/histaminereleasing factor via a nonclassical pathway, The Journal of biological chemistry, vol.279, pp.46104-46112, 2004.

T. Annoura, B. C. Van-schaijk, I. H. Ploemen, M. Sajid, J. W. Lin et al., Two Plasmodium 6-Cys familyrelated proteins have distinct and critical roles in liver-stage development, FASEB journal : official publication of the Federation of American Societies for Experimental Biology, vol.28, pp.2158-2170, 2014.

R. Arav-boger and T. A. Shapiro, Molecular mechanisms of resistance in antimalarial chemotherapy: the unmet challenge, Annual review of pharmacology and toxicology, vol.45, pp.565-585, 2005.

H. B. Armah, N. O. Wilson, B. Y. Sarfo, M. D. Powell, V. C. Bond et al., Cerebrospinal fluid and serum biomarkers of cerebral malaria mortality in Ghanaian children, Malaria journal, vol.6, p.147, 2007.

K. Artavanis-tsakonas, J. E. Tongren, and E. M. Riley, The war between the malaria parasite and the immune system: immunity, immunoregulation and immunopathology, Clinical and experimental immunology, vol.133, pp.145-152, 2003.

E. A. Ashley, M. Dhorda, R. M. Fairhurst, C. Amaratunga, P. Lim et al.,

S. Taylor, C. J. Yeung, J. A. Woodrow, D. Flegg, J. Das et al., Tracking Resistance to Artemisinin, Spread of artemisinin resistance in Plasmodium falciparum malaria, vol.371, pp.411-423, 2014.

C. Aucan, Y. Traore, F. Tall, B. Nacro, T. Traore-leroux et al., High immunoglobulin G2 (IgG2) and low IgG4 levels are associated with human resistance to Plasmodium falciparum malaria, Infection and immunity, vol.68, pp.1252-1258, 2000.
URL : https://hal.archives-ouvertes.fr/hal-01595926

A. Bachmann, C. Esser, M. Petter, S. Predehl, V. Kalckreuth et al., Absence of erythrocyte sequestration and lack of multicopy gene family expression in Plasmodium falciparum from a splenectomized malaria patient, PloS one, vol.4, p.7459, 2009.

J. K. Baird, Host age as a determinant of naturally acquired immunity to Plasmodium falciparum, Parasitology today, vol.11, pp.105-111, 1995.

D. M. Banic, J. Oliveira-ferreira, L. R. Pratt-riccio, V. Conseil, D. Goncalves et al., Immune response and lack of immune response to Plasmodium falciparum P126 antigen and its amino-terminal repeat in malariainfected humans, The American journal of tropical medicine and hygiene, vol.58, pp.768-774, 1998.

N. Bano, J. D. Romano, B. Jayabalasingham, and I. Coppens, Cellular interactions of Plasmodium liver stage with its host mammalian cell, International journal for parasitology, vol.37, pp.1329-1341, 2007.

L. Q. Bao, N. T. Huy, M. Kikuchi, T. Yanagi, M. Senba et al., CD19(+) B cells confer protection against experimental cerebral malaria in semi-immune rodent model, PloS one, vol.8, p.64836, 2013.
DOI : 10.1371/journal.pone.0064836
URL : https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0064836&type=printable

L. Q. Bao, D. M. Nhi, N. T. Huy, M. Kikuchi, T. Yanagi et al., Splenic CD11c+ cells derived from semi-immune mice protect naive mice against experimental cerebral malaria, Malaria journal, vol.14, p.23, 2015.
DOI : 10.1186/s12936-014-0533-y
URL : https://malariajournal.biomedcentral.com/track/pdf/10.1186/s12936-014-0533-y

D. L. Barber, E. J. Wherry, D. Masopust, B. Zhu, J. P. Allison et al., Restoring function in exhausted CD8 T cells during chronic viral infection, Nature, vol.439, pp.682-687, 2006.

A. E. Barry and A. Arnott, Strategies for designing and monitoring malaria vaccines targeting diverse antigens, Frontiers in immunology, vol.5, p.359, 2014.

L. K. Basco and J. L. Bras, In vitro reversal of chloroquine resistance with chlorpheniramine against African isolates of Plasmodium falciparum, Japanese journal of medical science & biology, vol.47, pp.59-63, 1994.

S. Basu, C. Quilici, H. H. Zhang, D. Grail, and A. R. Dunn, Mice lacking both G-CSF and IL-6 are more susceptible to Candida albicans infection: critical role of neutrophils in defense against Candida albicans, Growth factors, vol.26, pp.23-34, 2008.

H. P. Beck, D. Blake, M. L. Darde, I. Felger, S. Pedraza-diaz et al., Molecular approaches to diversity of populations of apicomplexan parasites, International journal for parasitology, vol.39, pp.175-189, 2009.
URL : https://hal.archives-ouvertes.fr/hal-00602917

W. Beghdadi, A. Porcherie, B. S. Schneider, D. Dubayle, R. Peronet et al., Inhibition of histamine-mediated signaling confers significant protection against severe malaria in mouse models of disease, The Journal of experimental medicine, vol.205, pp.395-408, 2008.

E. Belnoue, F. T. Costa, T. Frankenberg, A. M. Vigario, T. Voza et al., Protective T cell immunity against malaria liver stage after vaccination with live sporozoites under chloroquine treatment, Journal of immunology, vol.172, pp.2487-2495, 1950.

E. Belnoue, M. Kayibanda, A. M. Vigario, J. C. Deschemin, N. Van-rooijen et al., On the pathogenic role of brain-sequestered alphabeta CD8+ T cells in experimental cerebral malaria, Journal of immunology, vol.169, pp.6369-6375, 1950.

S. Bereczky, A. Dolo, B. Maiga, M. Hayano, F. Granath et al., Spleen enlargement and genetic diversity of Plasmodium falciparum infection in two ethnic groups with different malaria susceptibility in Mali, West Africa. Transactions of the Royal Society of Tropical Medicine and Hygiene, vol.100, pp.248-257, 2006.

S. Bereczky, S. M. Montgomery, M. Troye-blomberg, I. Rooth, M. A. Shaw et al., Elevated anti-malarial IgE in asymptomatic individuals is associated with reduced risk for subsequent clinical malaria, International journal for parasitology, vol.34, pp.935-942, 2004.

U. Bhattacharya, S. Roy, P. K. Kar, B. Sarangi, and S. C. Lahiri, Histamine & kinin system in experimental malaria, The Indian journal of medical research, vol.88, pp.558-563, 1988.

R. Bheekha-escura, D. W. Macglashan, J. M. Langdon, and S. M. Macdonald, Human recombinant histamine-releasing factor activates human eosinophils and the eosinophilic cell line, Blood, vol.96, pp.2191-2198, 2000.

J. Bhisutthibhan and S. R. Meshnick, Immunoprecipitation of [(3)H]dihydroartemisinin translationally controlled tumor protein (TCTP) adducts from Plasmodium falciparuminfected erythrocytes by using anti-TCTP antibodies, Antimicrobial agents and chemotherapy, vol.45, pp.2397-2399, 2001.

J. Bhisutthibhan, X. Q. Pan, P. A. Hossler, D. J. Walker, C. A. Yowell et al., The Plasmodium falciparum translationally controlled tumor protein homolog and its reaction with the antimalarial drug artemisinin, The Journal of biological chemistry, vol.273, pp.16192-16198, 1998.

J. Bhisutthibhan, M. A. Philbert, H. Fujioka, M. Aikawa, and S. R. Meshnick, The Plasmodium falciparum translationally controlled tumor protein: subcellular localization and calcium binding, European journal of cell biology, vol.78, pp.665-670, 1999.
DOI : 10.1016/s0171-9335(99)80052-1

E. M. Bijker, S. Borrmann, S. H. Kappe, B. Mordmuller, B. K. Sack et al., Novel approaches to whole sporozoite vaccination against malaria, Vaccine, vol.33, pp.7462-7468, 2015.

O. Billker, V. Lindo, M. Panico, A. E. Etienne, T. Paxton et al., Identification of xanthurenic acid as the putative inducer of malaria development in the mosquito, Nature, vol.392, pp.289-292, 1998.

L. Bini, H. Heid, S. Liberatori, G. Geier, V. Pallini et al., Two-dimensional gel electrophoresis of Caenorhabditis elegans homogenates and identification of protein spots by microsequencing, Electrophoresis, vol.18, pp.557-562, 1997.

S. D. Blackburn, H. Shin, W. N. Haining, T. Zou, C. J. Workman et al., Coregulation of CD8+ T cell exhaustion by multiple inhibitory receptors during chronic viral infection, Nature immunology, vol.10, pp.29-37, 2009.

H. Bohm, B. Gross, M. Gaestel, U. A. Bommer, G. Ryffel et al., The 5'-untranslated region of p23 mRNA from the Ehrlich ascites tumor is involved in translation control of the growth related protein p23, Biomedica biochimica acta, vol.50, pp.1193-1203, 1991.

U. Bommer and B. Thiele, The translationally controlled tumour protein (TCTP), The international journal of biochemistry & cell biology, vol.36, pp.379-385, 2004.
DOI : 10.1016/s1357-2725(03)00213-9

U. A. Bommer and B. J. Thiele, The translationally controlled tumour protein (TCTP), The international journal of biochemistry & cell biology, vol.36, pp.379-385, 2004.
DOI : 10.1016/s1357-2725(03)00213-9

L. Borish, R. Rosenbaum, L. Albury, and S. Clark, Activation of neutrophils by recombinant interleukin 6, Cellular immunology, vol.121, pp.280-289, 1989.
DOI : 10.1016/0008-8749(89)90026-9

H. Bouharoun-tayoun, P. Attanath, A. Sabchareon, T. Chongsuphajaisiddhi, and P. Druilhe, Antibodies that protect humans against Plasmodium falciparum blood stages do not on their own inhibit parasite growth and invasion in vitro, but act in cooperation with monocytes, The Journal of experimental medicine, vol.172, pp.1633-1641, 1990.

H. Bouharoun-tayoun and P. Druilhe, Plasmodium falciparum malaria: evidence for an isotype imbalance which may be responsible for delayed acquisition of protective immunity, Infection and immunity, vol.60, pp.1473-1481, 1992.

H. Bouharoun-tayoun, C. Oeuvray, F. Lunel, and P. Druilhe, Mechanisms underlying the monocyte-mediated antibody-dependent killing of Plasmodium falciparum asexual blood stages, The Journal of experimental medicine, vol.182, pp.409-418, 1995.

J. T. Bousema, L. C. Gouagna, C. J. Drakeley, A. M. Meutstege, B. A. Okech et al., Plasmodium falciparum gametocyte carriage in asymptomatic children in western Kenya, Malaria journal, vol.3, p.18, 2004.

E. Bouzigon, P. Forabosco, G. H. Koppelman, W. O. Cookson, M. H. Dizier et al., Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopy, European journal of human genetics : EJHG, vol.18, pp.700-706, 2010.
URL : https://hal.archives-ouvertes.fr/inserm-00748654

D. A. Brake, C. A. Long, and W. P. Weidanz, Adoptive protection against Plasmodium chabaudi adami malaria in athymic nude mice by a cloned T cell line, Journal of immunology, vol.140, pp.1989-1993, 1950.

S. Briquet, N. Lawson-hogban, B. Boisson, M. P. Soares, R. Peronet et al., Disruption of Parasite hmgb2 Gene Attenuates Plasmodium berghei ANKA Pathogenicity, vol.83, pp.2771-2784, 2015.

A. W. Brown, The insecticide-resistance problem: a review of developments in 1956 and 1957, Bulletin of the World Health Organization, vol.18, pp.309-321, 1958.

L. J. Bruce-chwatt, Essential malariology. William Heinemann Medical Books Ltd, vol.354, 1980.

O. Bruna-romero and A. Rodriguez, Dendritic cells can initiate protective immune responses against malaria, Infection and immunity, vol.69, pp.5173-5176, 2001.

P. A. Buffet, G. Safeukui, O. Milon, P. H. Mercereau-puijalon, and . David, Retention of erythrocytes in the spleen: a double-edged process in human malaria, Current opinion in hematology, vol.16, pp.157-164, 2009.

N. S. Butler, J. Moebius, L. L. Pewe, B. Traore, O. K. Doumbo et al., Therapeutic blockade of PD-L1 and LAG-3 rapidly clears established blood-stage Plasmodium infection, Nature immunology, vol.13, pp.188-195, 2012.

N. S. Butler, N. W. Schmidt, A. M. Vaughan, A. S. Aly, S. H. Kappe et al., Superior antimalarial immunity after vaccination with late liver stage-arresting genetically attenuated parasites, Cell host & microbe, vol.9, pp.451-462, 2011.

B. Calderon-perez, B. Xoconostle-cazares, R. Lira-carmona, R. Hernandez-rivas, J. Ortega-lopez et al., The Plasmodium falciparum translationally controlled tumor protein (TCTP) is incorporated more efficiently into B cells than its human homologue, PloS one, vol.9, p.85514, 2014.

C. Calissano, D. Modiano, B. S. Sirima, A. Konate, I. Sanou et al., IgE antibodies to Plasmodium falciparum and severity of malaria in children of one ethnic group living in Burkina Faso, The American journal of tropical medicine and hygiene, vol.69, pp.31-35, 2003.

C. Cans, B. J. Passer, V. Shalak, V. Nancy-portebois, V. Crible et al., Translationally controlled tumor protein acts as a guanine nucleotide dissociation inhibitor on the translation elongation factor eEF1A, Proceedings of the National Academy of Sciences of the United States of America, vol.100, pp.13892-13897, 2003.

J. Carlson, G. Holmquist, D. W. Taylor, P. Perlmann, and M. Wahlgren, Antibodies to a histidine-rich protein (PfHRP1) disrupt spontaneously formed Plasmodium falciparum erythrocyte rosettes, Proceedings of the National Academy of Sciences of the United States of America, vol.87, pp.2511-2515, 1990.

J. M. Carlton, J. H. Adams, J. C. Silva, S. L. Bidwell, H. Lorenzi et al.,

S. L. Sargeant, C. J. Salzberg, S. A. Stoeckert, M. M. Sullivan, S. L. Yamamoto et al., Comparative genomics of the neglected human malaria parasite Plasmodium vivax, Nature, vol.455, pp.757-763, 2008.

J. M. Carlton, S. V. Angiuoli, B. B. Suh, T. W. Kooij, M. Pertea et al.,

S. J. Bidwell, S. E. Shallom, S. B. Van-aken, T. V. Riedmuller, J. K. Feldblyum et al., Genome sequence and comparative analysis of the model rodent malaria parasite Plasmodium yoelii yoelii, Nature, vol.419, pp.512-519, 2002.

R. Carter and K. N. Mendis, Evolutionary and historical aspects of the burden of malaria, Clinical microbiology reviews, vol.15, pp.564-594, 2002.

J. Chae, I. Choi, and C. Kim, Homology modeling and molecular docking study of translationally controlled tumor protein and artemisinin, Archives of pharmacal research, vol.29, pp.50-58, 2006.

S. Charpian and J. M. Przyborski, Protein transport across the parasitophorous vacuole of Plasmodium falciparum: into the great wide open, Traffic, vol.9, pp.157-165, 2008.

R. Chattopadhyay, S. Conteh, M. Li, E. R. James, J. E. Epstein et al., The Effects of radiation on the safety and protective efficacy of an attenuated Plasmodium yoelii sporozoite malaria vaccine, Vaccine, vol.27, pp.3675-3680, 2009.

A. K. Chemtai, C. Hamers-casterman, R. Hamers, and P. D. Baetselier, T cell-mediated immunity in murine malaria. II. Induction of protective immunity to P. chabaudi by antigenfed macrophages and antigen-educated lymphocytes, Parasite immunology, vol.6, pp.469-480, 1984.

S. H. Chen, P. S. Wu, C. H. Chou, Y. T. Yan, H. Liu et al., A knockout mouse approach reveals that TCTP functions as an essential factor for cell proliferation and survival in a tissue-or cell type-specific manner, Molecular biology of the cell, vol.18, pp.2525-2532, 2007.

W. Chen and G. K. Khurana-hershey, Signal transducer and activator of transcription signals in allergic disease, The Journal of allergy and clinical immunology, vol.119, pp.542-523, 2007.

M. Cherif, D. Amoako-sakyi, A. Dolo, J. O. Pearson, B. Gyan et al., Distribution of FcgammaR gene polymorphisms among two sympatric populations in Mali: differing allele frequencies, associations with malariometric indices and implications for genetic susceptibility to malaria, Malaria journal, vol.15, p.29, 2016.

S. A. Chisholm, E. Mchugh, R. Lundie, M. W. Dixon, S. Ghosh et al., Contrasting Inducible Knockdown of the Auxiliary PTEX Component PTEX88 in P. falciparum and P. berghei Unmasks a Role in Parasite Virulence, PloS one, vol.11, p.149296, 2016.

S. T. Chitpatima, S. Makrides, R. Bandyopadhyay, and G. Brawerman, Nucleotide sequence of a major messenger RNA for a 21 kilodalton polypeptide that is under translational control in mouse tumor cells, Nucleic acids research, vol.16, p.2350, 1988.

P. Chomarat, J. Banchereau, J. Davoust, and A. K. Palucka, IL-6 switches the differentiation of monocytes from dendritic cells to macrophages, Nature immunology, vol.1, pp.510-514, 2000.

C. R. Chong, X. Chen, L. Shi, J. O. Liu, and D. J. Sullivan, A clinical drug library screen identifies astemizole as an antimalarial agent, Nature chemical biology, vol.2, pp.415-416, 2006.

S. Chung, M. Kim, W. Choi, J. Chung, and K. Lee, Expression of translationally controlled tumor protein mRNA in human colon cancer, Cancer letters, vol.156, pp.185-190, 2000.

I. A. Clark, K. A. Rockett, and W. B. Cowden, Proposed link between cytokines, nitric oxide and human cerebral malaria, Parasitology today, vol.7, pp.205-207, 1991.

C. Coban, K. J. Ishii, T. Kawai, H. Hemmi, S. Sato et al., Toll-like receptor 9 mediates innate immune activation by the malaria pigment hemozoin, The Journal of experimental medicine, vol.201, pp.19-25, 2005.

C. Coban, K. J. Ishii, S. Uematsu, N. Arisue, S. Sato et al., Pathological role of Toll-like receptor signaling in cerebral malaria, International immunology, vol.19, pp.67-79, 2007.

I. A. Cockburn, Y. C. Chen, M. G. Overstreet, J. R. Lees, N. Van-rooijen et al., Prolonged antigen presentation is required for optimal CD8+ T cell responses against malaria liver stage parasites, PLoS pathogens, vol.6, p.1000877, 2010.

S. Cohen, G. I. Mc, and S. Carrington, Gamma-globulin and acquired immunity to human malaria, Nature, vol.192, pp.733-737, 1961.

N. Coltel, V. Combes, N. H. Hunt, and G. E. Grau, Cerebral malaria-a neurovascular pathology with many riddles still to be solved, Current neurovascular research, vol.1, pp.91-110, 2004.

A. Coluzzi, The eradication of malaria. A world-wide challenge, 1961.

, Annali della sanita pubblica, vol.22, pp.241-253

L. M. Coronado, C. T. Nadovich, and C. Spadafora, Malarial hemozoin: from target to tool, Biochimica et biophysica acta, vol.1840, pp.2032-2041, 2014.
DOI : 10.1016/j.bbagen.2014.02.009
URL : http://europepmc.org/articles/pmc4049529?pdf=render

A. F. Cowman and B. S. Crabb, Invasion of red blood cells by malaria parasites, Cell, vol.124, pp.755-766, 2006.

D. Cox and S. Mcconkey, The role of platelets in the pathogenesis of cerebral malaria, Cellular and molecular life sciences : CMLS, vol.67, pp.557-568, 2010.

F. E. Cox, History of the discovery of the malaria parasites and their vectors, Parasites & vectors, vol.3, p.5, 2010.

J. Cox-singh, J. Hiu, S. B. Lucas, P. C. Divis, M. Zulkarnaen et al., Severe malaria-a case of fatal Plasmodium knowlesi infection with post-mortem findings: a case report, Malaria journal, vol.9, p.10, 2010.

I. N. Crispe, APC licensing and CD4+T cell help in liver-stage malaria, Frontiers in microbiology, vol.5, p.617, 2014.

P. D. Crompton, J. Moebius, S. Portugal, M. Waisberg, G. Hart et al., Malaria immunity in man and mosquito: insights into unsolved mysteries of a deadly infectious disease, Annual review of immunology, vol.32, pp.157-187, 2014.

D. Crotti, , 2005.

, Le infezioni in medicina : rivista periodica di eziologia, epidemiologia, diagnostica, vol.13, pp.265-270

C. B. Cunha and B. A. Cunha, Brief history of the clinical diagnosis of malaria: from Hippocrates to Osler, Journal of vector borne diseases, vol.45, pp.194-199, 2008.

D. 'ombrain, M. C. , L. J. Robinson, D. I. Stanisic, J. Taraika et al., Association of early interferon-gamma production with immunity to clinical malaria: a longitudinal study among Papua New Guinean children, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, vol.47, pp.1380-1387, 2008.

C. Daneshvar, T. M. Davis, J. Cox-singh, M. Z. Rafa'ee, S. K. Zakaria et al., Clinical and laboratory features of human Plasmodium knowlesi infection, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, vol.49, pp.852-860, 2009.

G. C. Davenport, C. Ouma, J. B. Hittner, T. Were, Y. Ouma et al., Hematological predictors of increased severe anemia in Kenyan children coinfected with Plasmodium falciparum and HIV-1, American journal of hematology, vol.85, pp.227-233, 2010.

P. H. David, M. Hommel, L. H. Miller, I. J. Udeinya, and L. D. Oligino, Parasite sequestration in Plasmodium falciparum malaria: spleen and antibody modulation of cytoadherence of infected erythrocytes, Proceedings of the National Academy of Sciences of the United States of America, vol.80, pp.5075-5079, 1983.

C. L. Day, D. E. Kaufmann, P. Kiepiela, J. A. Brown, E. S. Moodley et al.,

E. J. Altfeld, H. M. Wherry, P. J. Coovadia, P. Goulder, R. Klenerman et al., PD-1 expression on HIV-specific T cells is associated with T-cell exhaustion and disease progression, Nature, vol.443, pp.350-354, 2006.

T. F. De-koning-ward, C. J. Janse, and A. P. Waters, The development of genetic tools for dissecting the biology of malaria parasites, Annual review of microbiology, vol.54, pp.157-185, 2000.

M. De-niz, A. K. Ullrich, A. Heiber, A. Soares, C. Pick et al., The machinery underlying malaria parasite virulence is conserved between rodent and human malaria parasites, Nature communications, vol.7, p.11659, 2016.

D. Portillo, H. A. , M. Ferrer, T. Brugat, L. Martin-jaular et al., The role of the spleen in malaria, Cellular microbiology, vol.14, pp.343-355, 2012.

C. Demarta-gatsi, L. Smith, and S. Thiberge, Protection against malaria in mice is induced by blood stage-arresting histamine-releasing factor (HRF)-deficient parasites, vol.213, pp.1419-1428, 2016.
URL : https://hal.archives-ouvertes.fr/hal-01431690

C. E. Demeure, K. Brahimi, F. Hacini, F. Marchand, R. Peronet et al., Anopheles mosquito bites activate cutaneous mast cells leading to a local inflammatory response and lymph node hyperplasia, Journal of immunology, vol.174, pp.3932-3940, 1950.

R. S. Desowitz, Plasmodium-specific immunoglobulin E in sera from an area of holoendemic malaria, Transactions of the Royal Society of Tropical Medicine and Hygiene, vol.83, pp.478-479, 1989.

R. S. Desowitz, J. Elm, and M. P. Alpers, Plasmodium falciparum-specific immunoglobulin G (IgG), IgM, and IgE antibodies in paired maternal-cord sera from east Sepik Province, Infection and immunity, vol.61, pp.988-993, 1993.

S. Dewalick, F. H. Amante, K. A. Mcsweeney, L. M. Randall, A. C. Stanley et al., Cutting edge: conventional dendritic cells are the critical APC required for the induction of experimental cerebral malaria, Journal of immunology, vol.178, pp.6033-6037, 1950.

A. M. Dondorp, B. J. Angus, K. Chotivanich, K. Silamut, R. Ruangveerayuth et al., Red blood cell deformability as a predictor of anemia in severe falciparum malaria, The American journal of tropical medicine and hygiene, vol.60, pp.733-737, 1999.

A. M. Dondorp, S. J. Lee, M. A. Faiz, S. Mishra, R. Price et al., The relationship between age and the manifestations of and mortality associated with severe malaria, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, vol.47, pp.151-157, 2008.

D. L. Doolan, C. Dobano, and J. K. Baird, Acquired immunity to malaria, Clinical microbiology reviews, vol.22, pp.13-36, 2009.

D. L. Doolan and S. L. Hoffman, IL-12 and NK cells are required for antigen-specific adaptive immunity against malaria initiated by CD8+ T cells in the Plasmodium yoelii model, Journal of immunology, vol.163, pp.884-892, 1950.

D. L. Doolan and S. L. Hoffman, The complexity of protective immunity against liver-stage malaria, Journal of immunology, vol.165, pp.1453-1462, 1950.

J. R. Dorfman, P. Bejon, F. M. Ndungu, J. Langhorne, M. M. Kortok et al., B cell memory to 3 Plasmodium falciparum blood-stage antigens in a malaria-endemic area, The Journal of infectious diseases, vol.191, pp.1623-1630, 2005.

P. Dormer, M. Dietrich, P. Kern, and R. D. Horstmann, Ineffective erythropoiesis in acute human P. falciparum malaria, Blut, vol.46, pp.279-288, 1983.

P. Druilhe and J. L. Perignon, Mechanisms of defense against P. falciparum asexual blood stages in humans, Immunology letters, vol.41, pp.115-120, 1994.

M. El-far, R. Halwani, E. Said, L. Trautmann, M. Doroudchi et al., T-cell exhaustion in HIV infection, Current HIV/AIDS reports, vol.5, pp.13-19, 2008.

G. Elghazali, H. Perlmann, A. S. Rutta, P. Perlmann, and M. Troye-blomberg, Elevated plasma levels of IgE in Plasmodium falciparum-primed individuals reflect an increased ratio of IL-4 to interferon-gamma (IFN-gamma)-producing cells, Clinical and experimental immunology, vol.109, pp.84-89, 1997.

I. Ellinger and R. Fuchs, HFcRn-mediated transplacental immunoglobulin G transport: protection of and threat to the human fetus and newborn, Wiener medizinische Wochenschrift, vol.162, pp.207-213, 1946.

H. M. Elsheikha and N. A. Khan, Protozoa traversal of the blood-brain barrier to invade the central nervous system, FEMS microbiology reviews, vol.34, pp.532-553, 2010.

C. O. Enwonwu, B. M. Afolabi, L. A. Salako, E. O. Idigbe, H. Hassan et al., Hyperphenylalaninaemia in children with falciparum malaria, vol.92, pp.495-503, 1999.

C. O. Enwonwu, B. M. Afolabi, L. O. Salako, E. O. Idigbe, and N. Bashirelah, Increased plasma levels of histidine and histamine in falciparum malaria: relevance to severity of infection, Journal of neural transmission, vol.107, pp.1273-1287, 1996.

J. E. Epstein, K. Tewari, K. E. Lyke, B. K. Sim, P. F. Billingsley et al.,

C. F. Bennett, J. R. Ockenhouse, J. Murphy, N. Komisar, M. Thomas et al., Live attenuated malaria vaccine designed to protect through hepatic CD8(+) T cell immunity, Science, vol.334, pp.475-480, 2011.

A. A. Escalante and F. J. Ayala, Evolutionary origin of Plasmodium and other Apicomplexa based on rRNA genes, Proceedings of the National Academy of Sciences of the United States of America, vol.92, pp.5793-5797, 1995.

K. J. Evans, D. S. Hansen, N. Van-rooijen, L. A. Buckingham, and L. Schofield, Severe malarial anemia of low parasite burden in rodent models results from accelerated clearance of uninfected erythrocytes, Blood, vol.107, pp.1192-1199, 2006.

S. E. Farouk, A. Dolo, S. Bereczky, B. Kouriba, B. Maiga et al., Different antibody-and cytokine-mediated responses to Plasmodium falciparum parasite in two sympatric ethnic tribes living in Mali, Microbes and infection / Institut Pasteur, vol.7, pp.110-117, 2005.

N. Favre, B. Ryffel, G. Bordmann, and W. Rudin, The course of Plasmodium chabaudi chabaudi infections in interferon-gamma receptor deficient mice, Parasite immunology, vol.19, pp.375-383, 1997.

A. H. Fell, J. Currier, and M. F. Good, Inhibition of Plasmodium falciparum growth in vitro by CD4+ and CD8+ T cells from non-exposed donors, Parasite immunology, vol.16, pp.579-586, 1994.

Y. Feng, D. Liu, H. Yao, and J. Wang, Solution structure and mapping of a very weak calciumbinding site of human translationally controlled tumor protein by NMR, Archives of biochemistry and biophysics, vol.467, pp.48-57, 2007.

Z. Feng, L. Hensley, K. L. Mcknight, F. Hu, V. Madden et al., A pathogenic picornavirus acquires an envelope by hijacking cellular membranes, Nature, vol.496, pp.367-371, 2013.

M. U. Ferreira, M. Da-silva, G. Nunes, and . Wunderlich, Antigenic diversity and immune evasion by malaria parasites, Clinical and diagnostic laboratory immunology, vol.11, pp.987-995, 2004.

E. Ferroni, T. Jefferson, and G. Gachelin, Angelo Celli and research on the prevention of malaria in Italy a century ago, Journal of the Royal Society of Medicine, vol.105, pp.35-40, 2012.

G. Fiucci, A. Lespagnol, P. Stumptner-cuvelette, S. Beaucourt, D. Duflaut et al., Genomic organization and expression of mouse Tpt1 gene, Genomics, vol.81, pp.570-578, 2003.

L. Flori, B. Kumulungui, C. Aucan, C. Esnault, A. S. Traore et al., Linkage and association between Plasmodium falciparum blood infection levels and chromosome 5q31-q33, Genes and immunity, vol.4, pp.265-268, 2003.
URL : https://hal.archives-ouvertes.fr/hal-01595924

U. Frevert, S. Engelmann, S. Zougbede, J. Stange, B. Ng et al., Intravital observation of Plasmodium berghei sporozoite infection of the liver, PLoS biology, vol.3, p.192, 2005.

J. Friesen, O. Silvie, E. D. Putrianti, J. C. Hafalla, K. Matuschewski et al., Natural immunization against malaria: causal prophylaxis with antibiotics, Science translational medicine, vol.2, pp.40-49, 2010.
DOI : 10.1126/scitranslmed.3001058

C. Gabay and I. Kushner, Acute-phase proteins and other systemic responses to inflammation, The New England journal of medicine, vol.340, pp.448-454, 1999.
DOI : 10.1056/nejm199902113400607

Y. Gachet, S. Tournier, M. Lee, A. Lazaris-karatzas, T. Poulton et al., The growth-related, translationally controlled protein P23 has properties of a tubulin binding protein and associates transiently with microtubules during the cell cycle, Journal of cell science, vol.112, pp.1257-1271, 1999.

M. J. Gardner, N. Hall, E. Fung, O. White, M. Berriman et al., Genome sequence of the human malaria parasite Plasmodium falciparum, vol.419, pp.498-511, 2002.

M. J. Gardner, S. J. Shallom, J. M. Carlton, S. L. Salzberg, V. Nene et al., Nature, vol.419, pp.531-534, 2002.

O. Garraud, S. Mahanty, and R. Perraut, Malaria-specific antibody subclasses in immune individuals: a key source of information for vaccine design, Trends in immunology, vol.24, pp.30-35, 2003.
URL : https://hal.archives-ouvertes.fr/pasteur-00566841

J. Gauldie, C. Richards, D. Harnish, P. Lansdorp, and H. Baumann, Interferon beta 2/B-cell stimulatory factor type 2 shares identity with monocyte-derived hepatocyte-stimulating factor and regulates the major acute phase protein response in liver cells, Proceedings of the National Academy of Sciences of the United States of America, vol.84, pp.7251-7255, 1987.

D. Gaur, D. C. Mayer, and L. H. Miller, Parasite ligand-host receptor interactions during invasion of erythrocytes by Plasmodium merozoites, International journal for parasitology, vol.34, pp.1413-1429, 2004.

R. T. Gazzinelli, P. Kalantari, K. A. Fitzgerald, and D. T. Golenbock, Innate sensing of malaria parasites, Nature reviews. Immunology, vol.14, pp.744-757, 2014.

A. Ghumra, J. P. Semblat, R. S. Mcintosh, A. Raza, I. B. Rasmussen et al., Identification of residues in the Cmu4 domain of polymeric IgM essential for interaction with Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1), Journal of immunology, vol.181, pp.1988-2000, 1950.

E. N. Gitau and C. R. Newton, Review Article: blood-brain barrier in falciparum malaria, Tropical medicine & international health : TM & IH, vol.10, pp.285-292, 2005.

M. F. Good, J. M. Reiman, I. B. Rodriguez, K. Ito, S. K. Yanow et al., Crossspecies malaria immunity induced by chemically attenuated parasites, The Journal of clinical investigation, 2013.

P. Graidist, M. Yazawa, M. Tonganunt, A. Nakatomi, C. C. Lin et al., Fortilin binds Ca2+ and blocks Ca2+-dependent apoptosis in vivo, The Biochemical journal, vol.408, pp.181-191, 2007.

B. M. Greenwood, D. A. Fidock, D. E. Kyle, S. H. Kappe, P. L. Alonso et al., Malaria: progress, perils, and prospects for eradication, The Journal of clinical investigation, vol.118, pp.1266-1276, 2008.

B. M. Greenwood, F. Groenendaal, A. K. Bradley, A. M. Greenwood, F. Shenton et al., Ethnic differences in the prevalence of splenomegaly and malaria in The Gambia, Annals of tropical medicine and parasitology, vol.81, pp.345-354, 1987.

M. J. Griffiths, M. J. Shafi, S. J. Popper, C. A. Hemingway, M. M. Kortok et al., Genomewide analysis of the host response to malaria in Kenyan children, The Journal of infectious diseases, vol.191, pp.1599-1611, 2005.

M. P. Grobusch and P. G. Kremsner, Uncomplicated malaria, Current topics in microbiology and immunology, vol.295, pp.83-104, 2005.

H. Groux and J. Gysin, Opsonization as an effector mechanism in human protection against asexual blood stages of Plasmodium falciparum: functional role of IgG subclasses, Research in immunology, vol.141, pp.529-542, 1990.

E. Gruys, M. J. Toussaint, T. A. Niewold, and S. J. Koopmans, Acute phase reaction and acute phase proteins, Journal of Zhejiang University. Science. B, vol.6, pp.1045-1056, 2005.

P. Gueirard, J. Tavares, S. Thiberge, F. Bernex, T. Ishino et al., Development of the malaria parasite in the skin of the mammalian host, Proceedings of the National Academy of Sciences of the United States of America, vol.107, pp.18640-18645, 2010.

J. Gysin, S. Gavoille, D. Mattei, A. Scherf, S. Bonnefoy et al., In vitro phagocytosis inhibition assay for the screening of potential candidate antigens for sub-unit vaccines against the asexual blood stage of Plasmodium falciparum, Journal of immunological methods, vol.159, pp.209-219, 1993.

N. G. Haghighat and L. Ruben, Purification of novel calcium binding proteins from Trypanosoma brucei: properties of 22-, 24-and 38-kilodalton proteins, Molecular and biochemical parasitology, vol.51, pp.99-110, 1992.

A. Haileamlak, D. Dagoye, H. Williams, A. J. Venn, R. Hubbard et al., Early life risk factors for atopic dermatitis in Ethiopian children, The Journal of allergy and clinical immunology, vol.115, pp.370-376, 2005.

K. Haldar and N. Mohandas, Malaria, erythrocytic infection, and anemia. Hematology / the Education Program of the, pp.87-93, 2009.

N. Hall, M. Karras, J. D. Raine, J. M. Carlton, T. W. Kooij et al., A comprehensive survey of the Plasmodium life cycle by genomic, transcriptomic, and proteomic analyses, vol.307, pp.82-86, 2005.

A. A. Hamad, I. M. Hassan, A. A. Khalifa, G. I. Ahmed, S. A. Abdelrahim et al., Chronic Plasmodium falciparum infections in an area of low intensity malaria transmission in the Sudan, Parasitology, vol.120, pp.447-456, 2000.

D. S. Hansen, M. A. Siomos, T. D. Koning-ward, L. Buckingham, B. S. Crabb et al., CD1d-restricted NKT cells contribute to malarial splenomegaly and enhance parasitespecific antibody responses, European journal of immunology, vol.33, pp.2588-2598, 2003.
DOI : 10.1002/eji.200323666

A. Haque and C. Engwerda, Hepatocytes break the silence during liver-stage malaria, Nature medicine, vol.20, pp.17-19, 2014.

Z. Hawass, Y. Z. Gad, S. Ismail, R. Khairat, D. Fathalla et al., Ancestry and pathology in King Tutankhamun's family, vol.303, pp.638-647, 2010.
DOI : 10.1001/jama.2010.121
URL : https://jamanetwork.com/journals/jama/articlepdf/185393/joc05008_638_647.pdf

P. C. Heinrich, J. V. Castell, and T. Andus, Interleukin-6 and the acute phase response, The Biochemical journal, vol.265, pp.621-636, 1990.
DOI : 10.1042/bj2650621
URL : http://europepmc.org/articles/pmc1133681?pdf=render

H. Helmby, G. Jonsson, and M. Troye-blomberg, Cellular changes and apoptosis in the spleens and peripheral blood of mice infected with blood-stage Plasmodium chabaudi chabaudi AS, Infection and immunity, vol.68, pp.1485-1490, 2000.

H. Helmby, H. Perlmann, M. Troye-blomberg, and P. Perlmann, Immunoglobulin E elevation in Plasmodium chabaudi malaria, Infection and immunity, vol.64, pp.1432-1433, 1996.

M. Hensmann and D. Kwiatkowski, Cellular basis of early cytokine response to Plasmodium falciparum, Infection and immunity, vol.69, pp.2364-2371, 2001.

C. Hermsen, T. Van-de-wiel, E. Mommers, R. Sauerwein, and W. Eling, Depletion of CD4+ or CD8+ T-cells prevents Plasmodium berghei induced cerebral malaria in end-stage disease, Parasitology, vol.114, pp.7-12, 1997.

C. C. Hermsen, E. Mommers, T. Van-de-wiel, R. W. Sauerwein, and W. M. Eling, Convulsions due to increased permeability of the blood-brain barrier in experimental cerebral malaria can be prevented by splenectomy or anti-T cell treatment, The Journal of infectious diseases, vol.178, pp.1225-1227, 1998.

M. Hernandez-valladares, P. Rihet, O. K. Ole-moiyoi, and F. A. Iraqi, Mapping of a new quantitative trait locus for resistance to malaria in mice by a comparative mapping approach with human Chromosome 5q31-q33, Immunogenetics, vol.56, pp.115-117, 2004.
URL : https://hal.archives-ouvertes.fr/hal-01595919

A. V. Hill, C. E. Allsopp, D. Kwiatkowski, N. M. Anstey, P. Twumasi et al., Common west African HLA antigens are associated with protection from severe malaria, Nature, vol.352, pp.595-600, 1991.

J. Hinojosa-moya, B. Xoconostle-cazares, E. Piedra-ibarra, A. Mendez-tenorio, W. J. Lucas et al., Phylogenetic and structural analysis of translationally controlled tumor proteins, Journal of molecular evolution, vol.66, pp.472-483, 2008.

T. Hirano, K. Yasukawa, H. Harada, T. Taga, Y. Watanabe et al., Complementary DNA for a novel human interleukin (BSF-2) that induces B lymphocytes to produce immunoglobulin, Nature, vol.324, pp.73-76, 1986.

S. L. Hoffman, J. M. Crutcher, S. K. Puri, A. A. Ansari, F. Villinger et al., Sterile protection of monkeys against malaria after administration of interleukin-12, Nature medicine, vol.3, pp.80-83, 1997.

S. L. Hoffman, L. M. Goh, T. C. Luke, I. Schneider, T. P. Le et al., Protection of humans against malaria by immunization with radiation-attenuated Plasmodium falciparum sporozoites, The Journal of infectious diseases, vol.185, pp.1155-1164, 2002.

K. A. Hofmeyer, H. Jeon, and X. Zang, The PD-1/PD-L1 (B7-H1) pathway in chronic infectioninduced cytotoxic T lymphocyte exhaustion, Journal of biomedicine & biotechnology, p.451694, 2011.

J. Hoge, N. Yan, V. Janner, A. Schumacher, O. M. Chalaris et al., IL-6 controls the innate immune response against Listeria monocytogenes via classical IL-6 signaling, Journal of immunology, vol.190, pp.703-711, 1950.

J. M. Horne-debets, R. Faleiro, D. S. Karunarathne, X. Q. Liu, K. E. Lineburg et al., PD-1 dependent exhaustion of CD8+ T cells drives chronic malaria, Cell reports, vol.5, pp.1204-1213, 2013.

J. M. Horne-debets, D. S. Karunarathne, R. J. Faleiro, C. M. Poh, L. Renia et al., Mice lacking Programmed cell death-1 show a role for CD8(+) T cells in long-term immunity against blood-stage malaria, Scientific reports, vol.6, p.26210, 2016.

Y. C. Hsu, J. J. Chern, Y. Cai, M. Liu, and K. W. Choi, Drosophila TCTP is essential for growth and proliferation through regulation of dRheb GTPase, Nature, vol.445, pp.785-788, 2007.

X. Huang, K. Liew, O. Natalang, A. Siau, N. Zhang et al., The role of serine-type serine repeat antigen in Plasmodium yoelii blood stage development, PloS one, vol.8, p.60723, 2013.

N. H. Hunt, J. Golenser, T. Chan-ling, S. Parekh, C. Rae et al., Immunopathogenesis of cerebral malaria, International journal for parasitology, vol.36, pp.569-582, 2006.

N. H. Hunt and G. E. Grau, Cytokines: accelerators and brakes in the pathogenesis of cerebral malaria, Trends in immunology, vol.24, pp.491-499, 2003.

R. Idro, E. Bitarakwate, S. Tumwesigire, and C. C. John, Clinical manifestations of severe malaria in the highlands of southwestern Uganda, The American journal of tropical medicine and hygiene, vol.72, pp.561-567, 2005.

J. Illingworth, N. S. Butler, S. Roetynck, J. Mwacharo, S. K. Pierce et al., Chronic exposure to Plasmodium falciparum is associated with phenotypic evidence of B and T cell exhaustion, Journal of immunology, vol.190, pp.1038-1047, 1950.

J. Imanishi, Expression of cytokines in bacterial and viral infections and their biochemical aspects, Journal of biochemistry, vol.127, pp.525-530, 2000.

R. Ing and M. M. Stevenson, Dendritic cell and NK cell reciprocal cross talk promotes gamma interferon-dependent immunity to blood-stage Plasmodium chabaudi AS infection in mice, Infection and immunity, vol.77, pp.770-782, 2009.

S. Inoue, M. Niikura, S. Mineo, and F. Kobayashi, Roles of IFN-gamma and gammadelta T Cells in Protective Immunity Against Blood-Stage Malaria, Frontiers in immunology, vol.4, p.258, 2013.

Y. Ishida, Y. Agata, K. Shibahara, and T. Honjo, Induced expression of PD-1, a novel member of the immunoglobulin gene superfamily, upon programmed cell death, The EMBO journal, vol.11, pp.3887-3895, 1992.

S. K. Iyengar, K. B. Jacobs, and L. J. Palmer, Improved evidence for linkage on 6p and 5p with retrospective pooling of data from three asthma genome screens, Genetic epidemiology, vol.21, pp.130-135, 2001.

K. Jain, S. Sood, and K. Gowthamarajan, Modulation of cerebral malaria by curcumin as an adjunctive therapy. The Brazilian journal of infectious diseases : an official publication of the Brazilian Society of, Infectious Diseases, vol.17, pp.579-591, 2013.

C. J. Janse, J. Ramesar, and A. P. Waters, High-efficiency transfection and drug selection of genetically transformed blood stages of the rodent malaria parasite Plasmodium berghei, Nature protocols, vol.1, pp.346-356, 2006.

E. M. Janssen, E. E. Lemmens, T. Wolfe, U. Christen, M. G. Von-herrath et al., CD4+ T cells are required for secondary expansion and memory in CD8+ T lymphocytes, Nature, vol.421, pp.852-856, 2003.

O. Jobe, J. Lumsden, A. K. Mueller, J. Williams, H. Silva-rivera et al., Genetically attenuated Plasmodium berghei liver stages induce sterile protracted protection that is mediated by major histocompatibility complex Class I-dependent interferon-gamma-producing CD8+ T cells, The Journal of infectious diseases, vol.196, pp.599-607, 2007.

S. Jongwutiwes, C. Putaporntip, T. Iwasaki, M. U. Ferreira, H. Kanbara et al., Mitochondrial genome sequences support ancient population expansion in Plasmodium vivax, Molecular biology and evolution, vol.22, pp.1733-1739, 2005.

D. A. Joy, X. Feng, J. Mu, T. Furuya, K. Chotivanich et al., Early origin and recent expansion of Plasmodium falciparum, Science, vol.300, pp.318-321, 2003.

J. Jung, M. Kim, M. J. Kim, J. Kim, J. Moon et al., Translationally controlled tumor protein interacts with the third cytoplasmic domain of Na,K-ATPase alpha subunit and inhibits the pump activity in HeLa cells, The Journal of biological chemistry, vol.279, pp.49868-49875, 2004.

H. S. Kang, M. J. Lee, H. Song, S. H. Han, Y. M. Kim et al., Molecular identification of IgE-dependent histamine-releasing factor as a B cell growth factor, Journal of immunology, vol.166, pp.6545-6554, 1950.

S. H. Kappe, A. M. Vaughan, J. A. Boddey, and A. F. Cowman, That was then but this is now: malaria research in the time of an eradication agenda, Science, vol.328, pp.862-866, 2010.

J. C. Kashiwakura, T. Ando, K. Matsumoto, M. Kimura, J. Kitaura et al.,

. Kawakami, Histamine-releasing factor has a proinflammatory role in mouse models of asthma and allergy, The Journal of clinical investigation, vol.122, pp.218-228, 2012.

D. K. Kaul, E. F. Roth, R. L. Nagel, R. J. Howard, and S. M. Handunnetti, Rosetting of Plasmodium falciparum-infected red blood cells with uninfected red blood cells enhances microvascular obstruction under flow conditions, Blood, vol.78, pp.812-819, 1991.

C. C. Keller, O. Yamo, C. Ouma, J. M. Ong'echa, D. Ounah et al., Acquisition of hemozoin by monocytes down-regulates interleukin-12 p40 (IL12p40) transcripts and circulating IL-12p70 through an IL-10-dependent mechanism: in vivo and in vitro findings in severe malarial anemia, Infection and immunity, vol.74, pp.5249-5260, 2006.

S. M. Khan, C. J. Janse, S. H. Kappe, and S. A. Mikolajczak, Genetic engineering of attenuated malaria parasites for vaccination, Current opinion in biotechnology, vol.23, pp.908-916, 2012.

A. Kharazmi and S. Jepsen, Enhanced inhibition of in vitro multiplication of Plasmodium falciparum by stimulated human polymorphonuclear leucocytes, Clinical and experimental immunology, vol.57, pp.287-292, 1984.

M. Kim, Y. Jung, K. Lee, and C. Kim, Identification of the calcium binding sites in translationally controlled tumor protein, Archives of pharmacal research, vol.23, pp.633-636, 2000.

M. Kim, J. Maeng, and K. Lee, Dimerization of TCTP and its clinical implications for allergy, Biochimie, vol.95, pp.659-666, 2013.

M. Kim, H. J. Min, H. Y. Won, H. Park, J. C. Lee et al., Dimerization of translationally controlled tumor protein is essential for its cytokine-like activity, PloS one, vol.4, p.6464, 2009.

P. S. Kim and R. Ahmed, Features of responding T cells in cancer and chronic infection, Current opinion in immunology, vol.22, pp.223-230, 2010.

E. Y. Klein, Antimalarial drug resistance: a review of the biology and strategies to delay emergence and spread, International journal of antimicrobial agents, vol.41, pp.311-317, 2013.

N. Klonis, M. P. Crespo-ortiz, I. Bottova, N. Abu-bakar, S. Kenny et al., Artemisinin activity against Plasmodium falciparum requires hemoglobin uptake and digestion, Proceedings of the National Academy of Sciences of the United States of America, vol.108, pp.11405-11410, 2011.

Y. Kohara, K. Tanabe, K. Matsuoka, N. Kanda, H. Matsuda et al., A major determinant quantitative-trait locus responsible for atopic dermatitis-like skin lesions in NC/Nga mice is located on Chromosome 9, Immunogenetics, vol.53, pp.15-21, 2001.

Y. Koide, T. Kiyota, M. Tonganunt, D. Pinkaew, Z. Liu et al., Embryonic lethality of fortilin-null mutant mice by BMPpathway overactivation, Biochimica et biophysica acta, vol.1790, pp.326-338, 2009.

G. Krishnegowda, A. M. Hajjar, J. Zhu, E. J. Douglass, S. Uematsu et al., Induction of proinflammatory responses in macrophages by the glycosylphosphatidylinositols of Plasmodium falciparum: cell signaling receptors, glycosylphosphatidylinositol (GPI) structural requirement, and regulation of GPI activity, The Journal of biological chemistry, vol.280, pp.8606-8616, 2005.

R. Kumsiri, M. Troye-blomberg, K. Pattanapanyasat, S. Krudsood, and Y. Maneerat, IgE low affinity receptor (CD23) expression, Plasmodium falciparum specific IgE and tumor necrosis factor-alpha production in Thai uncomplicated and severe falciparum malaria patients, Acta tropica, vol.154, pp.25-33, 2016.

J. A. Kurtzhals, O. Rodrigues, M. Addae, J. O. Commey, F. K. Nkrumah et al., Reversible suppression of bone marrow response to erythropoietin in Plasmodium falciparum malaria, British journal of haematology, vol.97, pp.169-174, 1997.

S. Ladhani, B. Lowe, A. O. Cole, K. Kowuondo, and C. R. Newton, Changes in white blood cells and platelets in children with falciparum malaria: relationship to disease outcome, British journal of haematology, vol.119, pp.839-847, 2002.

J. M. Langdon, B. M. Vonakis, and S. M. Macdonald, Identification of the interaction between the human recombinant histamine releasing factor/translationally controlled tumor protein and elongation factor-1 delta (also known as eElongation factor-1B beta), Biochimica et biophysica acta, vol.1688, pp.232-236, 2004.

J. Langhorne, C. Cross, E. Seixas, C. Li, and T. Von-der-weid, A role for B cells in the development of T cell helper function in a malaria infection in mice, Proceedings of the National Academy of Sciences of the United States of America, vol.95, pp.1730-1734, 1998.

J. Langhorne, F. M. Ndungu, A. M. Sponaas, and K. Marsh, Immunity to malaria: more questions than answers, Nature immunology, vol.9, pp.725-732, 2008.

R. A. Leblanc, L. Pesnicak, E. S. Cabral, M. Godleski, and S. E. Straus, Lack of interleukin-6 (IL-6) enhances susceptibility to infection but does not alter latency or reactivation of herpes simplex virus type 1 in IL-6 knockout mice, Journal of virology, vol.73, pp.8145-8151, 1999.

R. F. Leke, R. R. Djokam, R. Mbu, R. J. Leke, J. Fogako et al., Detection of the Plasmodium falciparum antigen histidine-rich protein 2 in blood of pregnant women: implications for diagnosing placental malaria, Journal of clinical microbiology, vol.37, pp.2992-2996, 1999.

F. M. Leoratti, R. R. Durlacher, M. V. Lacerda, M. G. Alecrim, A. W. Ferreira et al., Pattern of humoral immune response to Plasmodium falciparum blood stages in individuals presenting different clinical expressions of malaria, Malaria journal, vol.7, p.186, 2008.

N. D. Levine, Progress in taxonomy of the Apicomplexan protozoa, The Journal of protozoology, vol.35, pp.518-520, 1988.

F. Li, D. Zhang, and K. Fujise, Characterization of fortilin, a novel antiapoptotic protein, The Journal of biological chemistry, vol.276, pp.47542-47549, 2001.

P. Liehl, V. Zuzarte-luis, J. Chan, T. Zillinger, F. Baptista et al., Host-cell sensors for Plasmodium activate innate immunity against liver-stage infection, vol.20, pp.47-53, 2014.

H. Liu, H. W. Peng, Y. S. Cheng, H. S. Yuan, and H. F. Yang-yen, Stabilization and enhancement of the antiapoptotic activity of mcl-1 by TCTP, Molecular and cellular biology, vol.25, pp.3117-3126, 2005.

D. E. Logie, I. A. Mcgregor, D. S. Rowe, and W. Z. Billewicz, Plasma immunoglobulin concentrations in mothers and newborn children with special reference to placental malaria: Studies in the Gambia, Bulletin of the World Health Organization, vol.49, pp.547-554, 1973.

S. Looareesuwan, M. Ho, Y. Wattanagoon, N. J. White, D. A. Warrell et al., Dynamic alteration in splenic function during acute falciparum malaria, The New England journal of medicine, vol.317, pp.675-679, 1987.

F. E. Lovegrove, S. A. Gharib, L. Pena-castillo, S. N. Patel, J. T. Ruzinski et al., Parasite burden and CD36-mediated sequestration are determinants of acute lung injury in an experimental malaria model, PLoS pathogens, vol.4, p.1000068, 2008.

T. C. Luke and S. L. Hoffman, Rationale and plans for developing a non-replicating, metabolically active, radiation-attenuated Plasmodium falciparum sporozoite vaccine, The Journal of experimental biology, vol.206, pp.3803-3808, 2003.

A. J. Luty, J. Mayombo, F. Lekoulou, and R. Mshana, Immunologic responses to soluble exoantigens of Plasmodium falciparum in Gabonese children exposed to continuous intense infection, The American journal of tropical medicine and hygiene, vol.51, pp.720-729, 1994.

A. J. Luty, D. J. Perkins, B. Lell, R. Schmidt-ott, L. G. Lehman et al., Low interleukin-12 activity in severe Plasmodium falciparum malaria, Infection and immunity, vol.68, pp.3909-3915, 2000.

S. M. Macdonald, J. Bhisutthibhan, T. A. Shapiro, S. J. Rogerson, T. E. Taylor et al., Immune mimicry in malaria: Plasmodium falciparum secretes a functional histamine-releasing factor homolog in vitro and in vivo, Proceedings of the National Academy of Sciences of the United States of America, vol.98, pp.10829-10832, 2001.

S. M. Macdonald, L. M. Lichtenstein, D. Proud, M. Plaut, R. M. Naclerio et al., Studies of IgE-dependent histamine releasing factors: heterogeneity of IgE, Journal of immunology, vol.139, pp.506-512, 1950.

S. M. Macdonald, T. Rafnar, J. Langdon, and L. M. Lichtenstein, Molecular identification of an IgE-dependent histamine-releasing factor, Science, vol.269, pp.688-690, 1995.

B. Maegraith and A. Fletcher, The pathogenesis of mammalian malaria, Advances in parasitology, vol.10, pp.49-75, 1972.

Y. Maeno, P. Perlmann, Y. Perlmannh, K. Kusuhara, T. Taniguchi et al., IgE deposition in brain microvessels and on parasitized erythrocytes from cerebral malaria patients, The American journal of tropical medicine and hygiene, vol.63, pp.128-132, 2000.

Y. Maeno, R. W. Steketee, T. Nagatake, T. Tegoshi, R. S. Desowitz et al., Immunoglobulin complex deposits in Plasmodium falciparum-infected placentas from Malawi and Papua New Guinea, The American journal of tropical medicine and hygiene, vol.49, pp.574-580, 1993.

A. G. Maier, B. M. Cooke, A. F. Cowman, and L. Tilley, Malaria parasite proteins that remodel the host erythrocyte, Nat Rev Microbiol, vol.7, pp.341-354, 2009.

A. Malek, R. Sager, P. Kuhn, K. H. Nicolaides, and H. Schneider, Evolution of maternofetal transport of immunoglobulins during human pregnancy, American journal of reproductive immunology, vol.36, pp.248-255, 1989.

E. Malkin, J. Hu, Z. Li, Z. Chen, X. Bi et al., A phase 1 trial of PfCP2.9: an AMA1/MSP1 chimeric recombinant protein vaccine for Plasmodium falciparum malaria, vol.26, pp.6864-6873, 2008.

M. K. Mannoor, R. C. Halder, S. R. Morshed, A. Ariyasinghe, H. Y. Bakir et al., Essential role of extrathymic T cells in protection against malaria, Journal of immunology, vol.169, pp.301-306, 1950.

D. G. Marsh, J. D. Neely, D. R. Breazeale, B. Ghosh, L. R. Freidhoff et al., Linkage analysis of IL4 and other chromosome 5q31.1 markers and total serum immunoglobulin E concentrations, Science, vol.264, pp.1152-1156, 1994.

K. Marsh and R. W. Snow, Host-parasite interaction and morbidity in malaria endemic areas, Philosophical transactions of the Royal Society of London. Series B, Biological sciences, vol.352, pp.1385-1394, 1997.

J. R. Matangila, J. Lufuluabo, A. L. Ibalanky, R. A. Inocencio-da-luz, P. Lutumba et al., Asymptomatic Plasmodium falciparum infection is associated with anaemia in pregnancy and can be more cost-effectively detected by rapid diagnostic test than by microscopy in Kinshasa, Democratic Republic of the Congo, Malaria journal, vol.13, p.132, 2014.

C. Mathieu, C. Demarta-gatsi, A. Porcherie, S. Brega, S. Thiberge et al., Plasmodium berghei histamine-releasing factor favours liver-stage development via inhibition of IL-6 production and associates with a severe outcome of disease, Cellular microbiology, vol.17, pp.542-558, 2015.

J. M. Matz, A. Ingmundson, J. C. Nunes, W. Stenzel, K. Matuschewski et al., Vivo Function of PTEX88 in Malaria Parasite Sequestration and Virulence, vol.14, pp.528-534, 2015.

M. B. Mccall, J. Hopman, M. Daou, B. Maiga, V. Dara et al., Early interferon-gamma response against Plasmodium falciparum correlates with interethnic differences in susceptibility to parasitemia between sympatric Fulani and Dogon in Mali, The Journal of infectious diseases, vol.201, pp.142-152, 2010.

J. S. Mccarthy, J. Marjason, S. Elliott, P. Fahey, G. Bang et al., A phase 1 trial of MSP2-C1, a blood-stage malaria vaccine containing 2 isoforms of MSP2 formulated with Montanide(R) ISA 720, PloS one, vol.6, p.24413, 2011.

R. S. Mcintosh, J. Shi, R. M. Jennings, J. C. Chappel, T. F. De-koning-ward et al., The importance of human FcgammaRI in mediating protection to malaria, PLoS pathogens, vol.3, p.72, 2007.

S. Mecheri, Contribution of allergic inflammatory response to the pathogenesis of malaria disease, Biochimica et biophysica acta, vol.1822, pp.49-56, 2012.

I. M. Medana and G. D. Turner, Human cerebral malaria and the blood-brain barrier, International journal for parasitology, vol.36, pp.555-568, 2006.

S. J. Meding, S. C. Cheng, B. Simon-haarhaus, and J. Langhorne, Role of gamma interferon during infection with Plasmodium chabaudi chabaudi, Infection and immunity, vol.58, pp.3671-3678, 1990.

R. Menard and V. Nussenzweig, Structure-function analysis of malaria proteins by gene targeting, Parasitology today, vol.16, pp.222-224, 2000.

S. R. Meshnick, Artemisinin: mechanisms of action, resistance and toxicity, International journal for parasitology, vol.32, pp.1655-1660, 2002.

D. A. Meyers, D. S. Postma, C. I. Panhuysen, J. Xu, P. J. Amelung et al., Evidence for a locus regulating total serum IgE levels mapping to chromosome 5, Genomics, vol.23, pp.464-470, 1994.

M. J. Micallef, T. Ohtsuki, K. Kohno, F. Tanabe, S. Ushio et al., Interferon-gamma-inducing factor enhances T helper 1 cytokine production by stimulated human T cells: synergism with interleukin-12 for interferon-gamma production, European journal of immunology, vol.26, pp.1647-1651, 1996.

L. H. Miller, D. I. Baruch, K. Marsh, and O. K. Doumbo, The pathogenic basis of malaria, Nature, vol.415, pp.673-679, 2002.

G. H. Mitchell, A. W. Thomas, G. Margos, A. R. Dluzewski, and L. H. Bannister, Apical membrane antigen 1, a major malaria vaccine candidate, mediates the close attachment of invasive merozoites to host red blood cells, Infection and immunity, vol.72, pp.154-158, 2004.

T. Miyagami, I. Igarshi, and M. Suzuki, Plasmodium berghei: long lasting immunity induced by a permanent attenuated mutant. Zentralblatt fur Bakteriologie, Mikrobiologie, und Hygiene. Series A, Medical microbiology, infectious diseases, virology, parasitology, vol.264, pp.502-512, 1987.

M. Miyakoda, D. Kimura, M. Yuda, Y. Chinzei, Y. Shibata et al., Malariaspecific and nonspecific activation of CD8+ T cells during blood stage of Plasmodium berghei infection, Journal of immunology, vol.181, pp.1420-1428, 1950.

D. Modiano, V. Petrarca, B. S. Sirima, I. Nebie, D. Diallo et al., Different response to Plasmodium falciparum malaria in west African sympatric ethnic groups, Proceedings of the National Academy of Sciences of the United States of America, vol.93, pp.13206-13211, 1996.

K. Mohan, P. Moulin, and M. M. Stevenson, Natural killer cell cytokine production, not cytotoxicity, contributes to resistance against blood-stage Plasmodium chabaudi AS infection, Journal of immunology, vol.159, pp.4990-4998, 1950.

L. Molineaux, M. Trauble, W. E. Collins, G. M. Jeffery, and K. Dietz, Malaria therapy reinoculation data suggest individual variation of an innate immune response and independent acquisition of antiparasitic and antitoxic immunities, Transactions of the Royal Society of Tropical Medicine and Hygiene, vol.96, pp.205-209, 2002.

C. Monso-hinard, J. N. Lou, C. Behr, P. Juillard, and G. E. Grau, Expression of major histocompatibility complex antigens on mouse brain microvascular endothelial cells in relation to susceptibility to cerebral malaria, Immunology, vol.92, pp.53-59, 1997.

A. Moody, Rapid diagnostic tests for malaria parasites, Clinical microbiology reviews, vol.15, pp.66-78, 2002.
DOI : 10.1128/cmr.15.1.66-78.2002
URL : https://cmr.asm.org/content/15/1/66.full.pdf

V. Moorthy and A. V. Hill, Malaria vaccines, Br Med Bull, vol.62, pp.59-72, 2002.

D. A. Morrison, Evolution of the Apicomplexa: where are we now?, Trends in parasitology, vol.25, pp.375-382, 2009.

M. M. Mota, G. Pradel, J. P. Vanderberg, J. C. Hafalla, U. Frevert et al., Migration of Plasmodium sporozoites through cells before infection, Science, vol.291, pp.141-144, 2001.

A. K. Mueller, N. Camargo, K. Kaiser, C. Andorfer, U. Frevert et al., Plasmodium liver stage developmental arrest by depletion of a protein at the parasitehost interface, Proceedings of the National Academy of Sciences of the United States of America, vol.102, pp.3022-3027, 2005.

A. K. Mueller, M. Deckert, K. Heiss, K. Goetz, K. Matuschewski et al., Genetically attenuated Plasmodium berghei liver stages persist and elicit sterile protection primarily via CD8 T cells, The American journal of pathology, vol.171, pp.107-115, 2007.

A. K. Mueller, M. Labaied, S. H. Kappe, and K. Matuschewski, Genetically modified Plasmodium parasites as a protective experimental malaria vaccine, Nature, vol.433, pp.164-167, 2005.

A. Muesch, E. Hartmann, K. Rohde, A. Rubartelli, R. Sitia et al., A novel pathway for secretory proteins, Trends in biochemical sciences, vol.15, pp.86-88, 1990.

E. Mundwiler-pachlatko and H. P. Beck, Maurer's clefts, the enigma of Plasmodium falciparum, Proceedings of the National Academy of Sciences of the United States of America, vol.110, pp.19987-19994, 2013.

J. M. Musser, J. S. Kroll, D. M. Granoff, E. R. Moxon, B. R. Brodeur et al., Global genetic structure and molecular epidemiology of encapsulated Haemophilus influenzae, Reviews of infectious diseases, vol.12, pp.75-111, 1990.

S. M. Muxel, A. P. Freitas-do-rosario, C. A. Zago, S. I. Castillo-mendez, L. R. Sardinha et al., The spleen CD4+ T cell response to blood-stage Plasmodium chabaudi malaria develops in two phases characterized by different properties, PloS one, vol.6, p.22434, 2011.

S. Nabi and S. Qader, Is Global Warming likely to cause an increased incidence of Malaria?, The Libyan journal of medicine, vol.4, pp.18-22, 2009.

C. Naing, M. A. Whittaker, V. N. Wai, and J. W. Mak, Is Plasmodium vivax malaria a severe malaria?: a systematic review and meta-analysis, PLoS neglected tropical diseases, vol.8, p.3071, 2014.

E. H. Nardin and R. S. Nussenzweig, T cell responses to pre-erythrocytic stages of malaria: role in protection and vaccine development against pre-erythrocytic stages, Annual review of immunology, vol.11, pp.687-727, 1993.

R. Ndyomugyenyi and P. Magnussen, Anaemia in pregnancy: Plasmodium falciparum infection is an important cause in primigravidae in Hoima district, western Uganda, Annals of tropical medicine and parasitology, vol.93, pp.457-465, 1999.

T. Nebl, M. J. De, L. Veer, and . Schofield, Stimulation of innate immune responses by malarial glycosylphosphatidylinositol via pattern recognition receptors, Parasitology, vol.130, pp.45-62, 2005.

M. E. Nelles, J. M. Moreau, C. L. Furlonger, A. Berger, J. A. Medin et al., Murine splenic CD4(+) T cells, induced by innate immune cell interactions and secreted factors, develop antileukemia cytotoxicity, Cancer immunology research, vol.2, pp.1113-1124, 2014.

K. Nganou-makamdop and R. W. Sauerwein, Liver or blood-stage arrest during malaria sporozoite immunization: the later the better?, Trends in parasitology, vol.29, pp.304-310, 2013.

M. Niikura, S. Inoue, S. Mineo, Y. Yamada, I. Kaneko et al., Experimental cerebral malaria is suppressed by disruption of nucleoside transporter 1 but not purine nucleoside phosphorylase, Biochemical and biophysical research communications, vol.432, pp.504-508, 2013.

A. Nussler, S. Pied, J. Goma, L. Renia, F. Miltgen et al., TNF inhibits malaria hepatic stages in vitro via synthesis of IL-6, International immunology, vol.3, pp.317-321, 1991.

R. K. Nyakundi, O. Nyamongo, J. Maamun, M. Akinyi, I. Mulei et al., Protective Effect of Chronic Schistosomiasis in Baboons Coinfected with Schistosoma mansoni and Plasmodium knowlesi, Infection and immunity, vol.84, pp.1320-1330, 2016.

C. Ocana-morgner, M. M. Mota, and A. Rodriguez, Malaria blood stage suppression of liver stage immunity by dendritic cells, The Journal of experimental medicine, vol.197, pp.143-151, 2003.

S. Oehen and K. Brduscha-riem, Differentiation of naive CTL to effector and memory CTL: correlation of effector function with phenotype and cell division, Journal of immunology, vol.161, pp.5338-5346, 1950.

B. R. Ogutu, O. J. Apollo, D. Mckinney, W. Okoth, J. Siangla et al.,

E. Martin, V. A. Angov, J. A. Stewart, D. G. Lyon, M. R. Heppner et al., Blood stage malaria vaccine eliciting high antigen-specific antibody concentrations confers no protection to young children in Western Kenya, PloS one, vol.4, p.4708, 2009.

T. Ohno, A. Ishih, Y. Kohara, H. Yonekawa, M. Terada et al., Chromosomal mapping of the host resistance locus to rodent malaria (Plasmodium yoelii) infection in mice, Immunogenetics, vol.53, pp.736-740, 2001.

I. Okamoto, K. Kohno, T. Tanimoto, H. Ikegami, and M. Kurimoto, Development of CD8+ effector T cells is differentially regulated by IL-18 and IL-12, Journal of immunology, vol.162, pp.3202-3211, 1950.

B. A. Okech, A. Nalunkuma, D. Okello, X. L. Pang, K. Suzue et al., Natural human immunoglobulin G subclass responses to Plasmodium falciparum serine repeat antigen in Uganda, The American journal of tropical medicine and hygiene, vol.65, pp.912-917, 2001.

G. A. Oliveira, K. A. Kumar, J. M. Calvo-calle, C. Othoro, D. Altszuler et al., Class II-restricted protective immunity induced by malaria sporozoites, Infection and immunity, vol.76, pp.1200-1206, 2008.

J. M. Oomen, J. H. Meuwissen, and W. Gemert, Differences in blood status of three ethnic groups inhabiting the same locality in Northern Nigeria. Anaemia, splenomegaly and associated causes, Tropical and geographical medicine, vol.31, pp.587-606, 1979.

A. S. Orago and C. A. Facer, Cytotoxicity of human natural killer (NK) cell subsets for Plasmodium falciparum erythrocytic schizonts: stimulation by cytokines and inhibition by neomycin, Clinical and experimental immunology, vol.86, pp.22-29, 1991.

M. G. Overstreet, Y. C. Chen, I. A. Cockburn, S. W. Tse, and F. Zavala, CD4+ T cells modulate expansion and survival but not functional properties of effector and memory CD8+ T cells induced by malaria sporozoites, PloS one, vol.6, p.15948, 2011.

R. M. Packard, The origins of antimalarial-drug resistance, The New England journal of medicine, vol.371, pp.397-399, 2014.

A. Pain, U. Bohme, A. E. Berry, K. Mungall, R. D. Finn et al., The genome of the simian and human malaria parasite Plasmodium knowlesi, vol.455, pp.799-803, 2008.

A. Pain, D. J. Ferguson, O. Kai, B. C. Urban, B. Lowe et al., Plateletmediated clumping of Plasmodium falciparum-infected erythrocytes is a common adhesive phenotype and is associated with severe malaria, Proceedings of the National Academy of Sciences of the United States of America, vol.98, pp.1805-1810, 2001.

M. E. Patarroyo, P. Romero, M. L. Torres, P. Clavijo, A. Moreno et al., Induction of protective immunity against experimental infection with malaria using synthetic peptides, Nature, vol.328, pp.629-632, 1987.

S. Pelleau, S. Diop, M. D. Badiane, J. Vitte, P. Beguin et al., Enhanced basophil reactivities during severe malaria and their relationship with the Plasmodium falciparum histamine-releasing factor translationally controlled tumor protein, Infection and immunity, vol.80, pp.2963-2970, 2012.

D. J. Perkins, J. B. Weinberg, and P. G. Kremsner, Reduced interleukin-12 and transforming growth factor-beta1 in severe childhood malaria: relationship of cytokine balance with disease severity, The Journal of infectious diseases, vol.182, pp.988-992, 2000.

D. J. Perkins, T. Were, G. C. Davenport, P. Kempaiah, J. B. Hittner et al., Severe malarial anemia: innate immunity and pathogenesis, International journal of biological sciences, vol.7, pp.1427-1442, 2011.

H. Perlmann, H. Helmby, M. Hagstedt, J. Carlson, P. H. Larsson et al., IgE elevation and IgE anti-malarial antibodies in Plasmodium falciparum malaria: association of high IgE levels with cerebral malaria, Clinical and experimental immunology, vol.97, pp.284-292, 1994.

P. Perlmann, H. Perlmann, G. Elghazali, and M. T. Blomberg, IgE and tumor necrosis factor in malaria infection, Immunology letters, vol.65, pp.29-33, 1999.

P. Perlmann, H. Perlmann, B. W. Flyg, M. Hagstedt, G. Elghazali et al., Immunoglobulin E, a pathogenic factor in Plasmodium falciparum malaria, Infection and immunity, vol.65, pp.116-121, 1997.

P. Perlmann, H. Perlmann, S. Looareesuwan, S. Krudsood, S. Kano et al., Contrasting functions of IgG and IgE antimalarial antibodies in uncomplicated and severe Plasmodium falciparum malaria, The American journal of tropical medicine and hygiene, vol.62, pp.373-377, 2000.

P. Perlmann and M. Troye-blomberg, Malaria and the immune system in humans, Chemical immunology, vol.80, pp.229-242, 2002.

J. A. Perry, A. Rush, R. J. Wilson, C. S. Olver, and A. C. Avery, Dendritic cells from malariainfected mice are fully functional APC, Journal of immunology, vol.172, pp.475-482, 1950.

S. Pied, A. Nussler, M. Pontent, F. Miltgen, H. Matile et al., C-reactive protein protects against preerythrocytic stages of malaria, Infection and immunity, vol.57, pp.278-282, 1989.

S. Pied, L. Renia, A. Nussler, F. Miltgen, and D. Mazier, Inhibitory activity of IL-6 on malaria hepatic stages, Parasite immunology, vol.13, pp.211-217, 1991.

S. Pied, J. Roland, A. Louise, D. Voegtle, V. Soulard et al., Liver CD4-CD8-NK1.1+ TCR alpha beta intermediate cells increase during experimental malaria infection and are able to exhibit inhibitory activity against the parasite liver stage in vitro, Journal of immunology, vol.164, pp.1463-1469, 1950.

P. Pino, N. Vouldoukis, M. Dugas, J. Conti, B. Nitcheu et al., Induction of the CD23/nitric oxide pathway in endothelial cells downregulates ICAM-1 expression and decreases cytoadherence of Plasmodium falciparum-infected erythrocytes, Cellular microbiology, vol.6, pp.839-848, 2004.

A. Pinzon-charry, V. Mcphun, V. Kienzle, C. Hirunpetcharat, C. Engwerda et al., Low doses of killed parasite in CpG elicit vigorous CD4+ T cell responses against blood-stage malaria in mice, The Journal of clinical investigation, vol.120, pp.2967-2978, 2010.

L. Piva, P. Tetlak, C. Claser, K. Karjalainen, L. Renia et al., Cutting edge: Clec9A+ dendritic cells mediate the development of experimental cerebral malaria, Journal of immunology, vol.189, pp.1128-1132, 1950.

T. Planche, A. Dzeing, E. Ngou-milama, M. Kombila, and P. W. Stacpoole, Metabolic complications of severe malaria, Current topics in microbiology and immunology, vol.295, pp.105-136, 2005.
DOI : 10.1007/3-540-29088-5_5

A. E. Platonov, G. A. Shipulin, I. V. Vershinina, J. Dankert, J. G. Van-de-winkel et al., Association of human Fc gamma RIIa (CD32) polymorphism with susceptibility to and severity of meningococcal disease, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, vol.27, pp.746-750, 1998.

D. Plouffe, A. Brinker, C. Mcnamara, K. Henson, N. Kato et al.,

P. G. Caldwell, Y. Schultz, E. A. Zhou, and . Winzeler, In silico activity profiling reveals the mechanism of action of antimalarials discovered in a high-throughput screen, Proc Natl Acad Sci U S A, vol.105, pp.9059-9064, 2008.

M. Polimeni and M. Prato, Host matrix metalloproteinases in cerebral malaria: new kids on the block against blood-brain barrier integrity? Fluids and barriers of the CNS, vol.11, 2014.

D. J. Pombo, G. Lawrence, C. Hirunpetcharat, C. Rzepczyk, M. Bryden et al., Immunity to malaria after administration of ultra-low doses of red cells infected with Plasmodium falciparum, The Lancet, vol.360, pp.610-617, 2002.

M. Poorafshar, H. Helmby, M. Troye-blomberg, and L. Hellman, MMCP-8, the first lineagespecific differentiation marker for mouse basophils. Elevated numbers of potent IL-4producing and MMCP-8-positive cells in spleens of malaria-infected mice, European journal of immunology, vol.30, pp.2660-2668, 2000.

A. Porcherie, C. Mathieu, R. Peronet, E. Schneider, J. Claver et al., Critical role of the neutrophil-associated high-affinity receptor for IgE in the pathogenesis of experimental cerebral malaria, The Journal of experimental medicine, vol.208, pp.2225-2236, 2011.
URL : https://hal.archives-ouvertes.fr/hal-00629378

F. Porichis and D. E. Kaufmann, Role of PD-1 in HIV pathogenesis and as target for therapy, Current HIV/AIDS reports, vol.9, pp.81-90, 2012.

D. S. Postma, E. R. Bleecker, P. J. Amelung, K. J. Holroyd, J. Xu et al., Genetic susceptibility to asthma-bronchial hyperresponsiveness coinherited with a major gene for atopy, The New England journal of medicine, vol.333, pp.894-900, 1995.

D. Prakash, C. Fesel, R. Jain, P. A. Cazenave, G. C. Mishra et al., Clusters of cytokines determine malaria severity in Plasmodium falciparum-infected patients from endemic areas of Central India, The Journal of infectious diseases, vol.194, pp.198-207, 2006.

R. N. Price, J. A. Simpson, F. Nosten, C. Luxemburger, L. Hkirjaroen et al., Factors contributing to anemia after uncomplicated falciparum malaria, The American journal of tropical medicine and hygiene, vol.65, pp.614-622, 2001.

C. Proietti and D. L. Doolan, The case for a rational genome-based vaccine against malaria, Frontiers in microbiology, vol.5, p.741, 2014.

F. Prugnolle, P. Durand, C. Neel, B. Ollomo, F. J. Ayala et al., African great apes are natural hosts of multiple related malaria species, including Plasmodium falciparum, Proceedings of the National Academy of Sciences of the United States of America, vol.107, pp.1458-1463, 2010.

E. D. Putrianti, A. Schmidt-christensen, I. Arnold, V. T. Heussler, K. Matuschewski et al., The Plasmodium serine-type SERA proteases display distinct expression patterns and non-essential in vivo roles during life cycle progression of the malaria parasite, Cellular microbiology, vol.12, pp.725-739, 2010.

E. D. Putrianti, O. Silvie, M. Kordes, S. Borrmann, and K. Matuschewski, Vaccine-like immunity against malaria by repeated causal-prophylactic treatment of liver-stage Plasmodium parasites, The Journal of infectious diseases, vol.199, pp.899-903, 2009.

J. U. Que, S. J. Cryz, R. Ballou, E. Furer, M. Gross et al., Effect of carrier selection on immunogenicity of protein conjugate vaccines against Plasmodium falciparum circumsporozoites, Infection and immunity, vol.56, pp.2645-2649, 1988.

T. C. Quinn and D. J. Wyler, Mechanisms of action of hyperimmune serum in mediating protective immunity to rodent malaria (Plasmodium berghei), Journal of immunology, vol.123, pp.2245-2249, 1950.

G. S. Rajahram, B. E. Barber, T. William, M. J. Grigg, J. Menon et al., Falling Plasmodium knowlesi Malaria Death Rate among Adults despite Rising Incidence, Emerging infectious diseases, vol.22, pp.41-48, 2010.

G. Ramadori, J. Van-damme, H. Rieder, and K. H. Meyer-zum-buschenfelde, Interleukin 6, the third mediator of acute-phase reaction, modulates hepatic protein synthesis in human and mouse. Comparison with interleukin 1 beta and tumor necrosis factor-alpha, European journal of immunology, vol.18, pp.1259-1264, 1988.

V. Ramakrishnaiah, C. Thumann, I. Fofana, F. Habersetzer, Q. Pan et al., Exosome-mediated transmission of hepatitis C virus between human hepatoma Huh7.5 cells, Proceedings of the National Academy of Sciences of the United States of America, vol.110, pp.13109-13113, 2013.

R. S. Ramiro, S. E. Reece, and D. J. Obbard, Molecular evolution and phylogenetics of rodent malaria parasites, BMC evolutionary biology, vol.12, p.219, 2012.

G. Raposo and W. Stoorvogel, Extracellular vesicles: exosomes, microvesicles, and friends, The Journal of cell biology, vol.200, pp.373-383, 2013.
DOI : 10.1083/jcb.201211138
URL : http://jcb.rupress.org/content/200/4/373.full.pdf

L. Renia, S. M. Potter, M. Mauduit, D. S. Rosa, M. Kayibanda et al., Pathogenic T cells in cerebral malaria, International journal for parasitology, vol.36, pp.547-554, 2006.

B. A. Rhein, L. S. Powers, K. Rogers, M. Anantpadma, B. K. Singh et al., Interferon-gamma Inhibits Ebola Virus Infection, PLoS pathogens, vol.11, p.1005263, 2015.
DOI : 10.1371/journal.ppat.1005263
URL : https://journals.plos.org/plospathogens/article/file?id=10.1371/journal.ppat.1005263&type=printable

S. B. Rho, J. H. Lee, M. S. Park, H. J. Byun, S. Kang et al., Antiapoptotic protein TCTP controls the stability of the tumor suppressor p53, FEBS letters, vol.585, pp.29-35, 2011.

J. S. Richards and J. G. Beeson, The future for blood-stage vaccines against malaria, Immunology and cell biology, vol.87, pp.377-390, 2009.

T. L. Richie, P. F. Billingsley, B. K. Sim, E. R. James, S. Chakravarty et al., Progress with Plasmodium falciparum sporozoite (PfSPZ)-based malaria vaccines, vol.33, pp.7452-7461, 2015.

P. Rihet, Y. Traore, L. Abel, C. Aucan, T. Traore-leroux et al., Malaria in humans: Plasmodium falciparum blood infection levels are linked to chromosome 5q31-q33, American journal of human genetics, vol.63, pp.498-505, 1998.
URL : https://hal.archives-ouvertes.fr/hal-01595931

A. Robert, Y. Coppel, and B. Meunier, Alkylation of heme by the antimalarial drug artemisinin, Chemical communications, pp.414-415, 2002.

M. Roestenberg, M. Mccall, J. Hopman, J. Wiersma, A. J. Luty et al., Protection against a malaria challenge by sporozoite inoculation, The New England journal of medicine, vol.361, pp.468-477, 2009.

J. A. Rowe, A. Claessens, R. A. Corrigan, and M. Arman, Adhesion of Plasmodium falciparuminfected erythrocytes to human cells: molecular mechanisms and therapeutic implications, Expert reviews in molecular medicine, vol.11, p.16, 2009.

J. A. Rowe and S. A. Kyes, The role of Plasmodium falciparum var genes in malaria in pregnancy, Molecular microbiology, vol.53, pp.1011-1019, 2004.

J. A. Rowe, J. Shafi, O. K. Kai, K. Marsh, and A. Raza, Nonimmune IgM, but not IgG binds to the surface of Plasmodium falciparum-infected erythrocytes and correlates with rosetting and severe malaria, The American journal of tropical medicine and hygiene, vol.66, pp.692-699, 2002.

R. and S. C. , Efficacy and safety of RTS,S/AS01 malaria vaccine with or without a booster dose in infants and children in Africa: final results of a phase 3, individually randomised, controlled trial, Lancet, vol.386, pp.31-45, 2015.

M. A. Ruffer, Studies in palaeopathology in Egypt, The Journal of Pathology and Bacteriology, vol.18, pp.149-162, 1913.

N. Rujeni, N. Nausch, N. Midzi, R. Gwisai, T. Mduluza et al., Soluble CD23 levels are inversely associated with atopy and parasite-specific IgE levels but not with polyclonal IgE levels in people exposed to helminth infection, International archives of allergy and immunology, vol.161, pp.333-341, 2013.
DOI : 10.1159/000346545
URL : http://europepmc.org/articles/pmc3795451?pdf=render

J. Sachs and P. Malaney, The economic and social burden of malaria, Nature, vol.415, pp.680-685, 2002.

I. Sagara, A. Dicko, R. D. Ellis, M. P. Fay, S. I. Diawara et al., A randomized controlled phase 2 trial of the blood stage AMA1-C1/Alhydrogel malaria vaccine in children in Mali, vol.27, pp.3090-3098, 2009.

A. Sakuntabhai, R. Ndiaye, I. Casademont, C. Peerapittayamongkol, C. Rogier et al., Genetic determination and linkage mapping of Plasmodium falciparum malaria related traits in Senegal, PloS one, vol.3, p.2000, 2008.

H. Sam and M. M. Stevenson, Early IL-12 p70, but not p40, production by splenic macrophages correlates with host resistance to blood-stage Plasmodium chabaudi AS malaria, Clinical and experimental immunology, vol.117, pp.343-349, 1999.

H. Sam and M. M. Stevenson, In vivo IL-12 production and IL-12 receptors beta1 and beta2 mRNA expression in the spleen are differentially up-regulated in resistant B6 and susceptible A/J mice during early blood-stage Plasmodium chabaudi AS malaria, Journal of immunology, vol.162, pp.1582-1589, 1950.

L. A. Sanni, L. F. Fonseca, and J. Langhorne, Mouse models for erythrocytic-stage malaria, Methods in molecular medicine, vol.72, pp.57-76, 2002.

A. Scherf, J. J. Lopez-rubio, and L. Riviere, Antigenic variation in Plasmodium falciparum, Annual review of microbiology, vol.62, pp.445-470, 2008.

J. Schmieg, G. Gonzalez-aseguinolaza, and M. Tsuji, The role of natural killer T cells and other T cell subsets against infection by the pre-erythrocytic stages of malaria parasites, Microbes and infection / Institut Pasteur, vol.5, pp.499-506, 2003.

B. S. Schneider, C. Mathieu, R. Peronet, and S. Mecheri, Anopheles stephensi saliva enhances progression of cerebral malaria in a murine model. Vector borne and zoonotic diseases, vol.11, pp.423-432, 2011.

L. Schofield and G. E. Grau, Immunological processes in malaria pathogenesis, Nature reviews. Immunology, vol.5, pp.722-735, 2005.

L. Schofield and F. Hackett, Signal transduction in host cells by a glycosylphosphatidylinositol toxin of malaria parasites, The Journal of experimental medicine, vol.177, pp.145-153, 1993.

L. Schofield, S. Novakovic, P. Gerold, R. T. Schwarz, M. J. Mcconville et al., Glycosylphosphatidylinositol toxin of Plasmodium up-regulates intercellular adhesion molecule-1, vascular cell adhesion molecule-1, and E-selectin expression in vascular endothelial cells and increases leukocyte and parasite cytoadherence via tyrosine kinasedependent signal transduction, Journal of immunology, vol.156, pp.1886-1896, 1950.

L. Schofield, J. Villaquiran, A. Ferreira, H. Schellekens, R. Nussenzweig et al., Gamma interferon, CD8+ T cells and antibodies required for immunity to malaria sporozoites, Nature, vol.330, pp.664-666, 1987.

J. Schrevel, G. Asfaux-foucher, J. M. Hopkins, V. Robert, C. Bourgouin et al., Vesicle trafficking during sporozoite development in Plasmodium berghei: ultrastructural evidence for a novel trafficking mechanism, Parasitology, vol.135, pp.1-12, 2008.

J. T. Schroeder, L. M. Lichtenstein, and S. M. Macdonald, Recombinant histamine-releasing factor enhances IgE-dependent IL-4 and IL-13 secretion by human basophils, Journal of immunology, vol.159, pp.447-452, 1950.

R. R. Schumann, Malarial fever: hemozoin is involved but Toll-free, Proceedings of the National Academy of Sciences of the United States of America, vol.104, pp.1743-1744, 2007.

J. D. Schwarzmeier, R. Hubmann, M. Duchler, U. Jager, and M. Shehata, Regulation of CD23 expression by Notch2 in B-cell chronic lymphocytic leukemia, Leukemia & lymphoma, vol.46, pp.157-165, 2005.

R. A. Seder, L. J. Chang, M. E. Enama, K. L. Zephir, U. N. Sarwar et al.,

S. L. Graham and . Hoffman, Protection against malaria by intravenous immunization with a nonreplicating sporozoite vaccine, Science, vol.341, pp.1359-1365, 2013.

J. Seka-seka, Y. Brouh, A. C. Yapo-crezoit, and N. H. Atseye, The role of serum immunoglobulin E in the pathogenesis of Plasmodium falciparum malaria in Ivorian children, Scandinavian journal of immunology, vol.59, pp.228-230, 2004.

E. Sergent and L. Parrot, L'immunite, la premunition et la resistance innee, Arch. Inst. Pasteur Algerie, vol.13, pp.279-319, 1935.

L. Serghides, T. G. Smith, S. N. Patel, and K. C. Kain, CD36 and malaria: friends or foes?, Trends in parasitology, vol.19, pp.461-469, 2003.

B. A. Sherry, G. Alava, K. J. Tracey, J. Martiney, A. Cerami et al., Malaria-specific metabolite hemozoin mediates the release of several potent endogenous pyrogens (TNF, MIP1 alpha, and MIP-1 beta) in vitro, and altered thermoregulation in vivo, Journal of inflammation, vol.45, pp.85-96, 1995.

P. Shetty, The numbers game, Nature, vol.484, pp.14-15, 2012.

Y. P. Shi, B. L. Nahlen, S. Kariuki, K. B. Urdahl, P. D. Mcelroy et al., Fcgamma receptor IIa (CD32) polymorphism is associated with protection of infants against high-density Plasmodium falciparum infection. VII. Asembo Bay Cohort Project, The Journal of infectious diseases, vol.184, pp.107-111, 2001.

Y. P. Shi, V. Udhayakumar, A. J. Oloo, B. L. Nahlen, and A. A. , Differential effect and interaction of monocytes, hyperimmune sera, and immunoglobulin G on the growth of asexual stage Plasmodium falciparum parasites, The American journal of tropical medicine and hygiene, vol.60, pp.135-141, 1999.

W. A. Siddiqui, L. Q. Tam, K. J. Kramer, G. S. Hui, S. E. Case et al., Merozoite surface coat precursor protein completely protects Aotus monkeys against Plasmodium falciparum malaria, Proceedings of the National Academy of Sciences of the United States of America, vol.84, pp.3014-3018, 1987.

O. Silvie, J. P. Semblat, J. F. Franetich, L. Hannoun, W. Eling et al., Effects of irradiation on Plasmodium falciparum sporozoite hepatic development: implications for the design of pre-erythrocytic malaria vaccines, Parasite immunology, vol.24, pp.221-223, 2002.

B. Singh, L. K. Sung, A. Matusop, A. Radhakrishnan, S. S. Shamsul et al., A large focus of naturally acquired Plasmodium knowlesi infections in human beings, Lancet, vol.363, pp.1017-1024, 2004.

A. Sowunmi, A. I. Ayede, A. G. Falade, V. N. Ndikum, C. O. Sowunmi et al., Randomized comparison of chloroquine and amodiaquine in the treatment of acute, uncomplicated, Plasmodium falciparum malaria in children, Annals of tropical medicine and parasitology, vol.95, pp.549-558, 2001.

A. Sowunmi, G. O. Gbotosho, C. T. Happi, A. A. Adedeji, O. M. Bolaji et al., Enhancement of the antimalarial efficacy of amodiaquine by chlorpheniramine in vivo, Memorias do Instituto Oswaldo Cruz, vol.102, pp.417-419, 2007.

A. Sowunmi, A. M. Oduola, O. A. Ogundahunsi, C. O. Falade, G. O. Gbotosho et al., Enhanced efficacy of chloroquine-chlorpheniramine combination in acute uncomplicated falciparum malaria in children, Transactions of the Royal Society of Tropical Medicine and Hygiene, vol.91, pp.63-67, 1997.

A. Sowunmi, A. M. Oduola, O. A. Ogundahunsi, and L. A. Salako, Comparative efficacy of chloroquine plus chlorpheniramine and pyrimethamine/sulfadoxine in acute uncomplicated falciparum malaria in Nigerian children, Transactions of the Royal Society of Tropical Medicine and Hygiene, vol.92, pp.77-81, 1998.

A. Sowunmi, A. M. Oduola, O. A. Ogundahunsi, and L. A. Salako, Enhancement of the antimalarial effect of chloroquine by chloropheniramine in vivo, Tropical medicine & international health : TM & IH, vol.3, pp.177-183, 1998.

R. Spaccapelo, E. Aime, S. Caterbi, P. Arcidiacono, B. Capuccini et al., Disruption of plasmepsin-4 and merozoites surface protein-7 genes in Plasmodium berghei induces combined virulence-attenuated phenotype, Scientific reports, vol.1, p.39, 2011.

R. Spaccapelo, C. J. Janse, S. Caterbi, B. Franke-fayard, J. A. Bonilla et al., Plasmepsin 4-deficient Plasmodium berghei are virulence attenuated and induce protective immunity against experimental malaria, The American journal of pathology, vol.176, pp.205-217, 2010.

A. M. Sponaas, E. T. Cadman, C. Voisine, V. Harrison, A. Boonstra et al., Malaria infection changes the ability of splenic dendritic cell populations to stimulate antigen-specific T cells, The Journal of experimental medicine, vol.203, pp.1427-1433, 2006.

A. M. Sponaas, A. P. Freitas-do-rosario, C. Voisine, B. Mastelic, J. Thompson et al., Migrating monocytes recruited to the spleen play an important role in control of blood stage malaria, Blood, vol.114, pp.5522-5531, 2009.

M. Spring, J. Murphy, R. Nielsen, M. Dowler, J. W. Bennett et al., First-in-human evaluation of genetically attenuated Plasmodium falciparum sporozoites administered by bite of Anopheles mosquitoes to adult volunteers, Vaccine, vol.31, pp.4975-4983, 2013.

T. Srichaikul, N. Archararit, T. Siriasawakul, and T. Viriyapanich, Histamine changes in Plasmodium falciparum malaria, Transactions of the Royal Society of Tropical Medicine and Hygiene, vol.70, pp.36-38, 1976.

D. I. Stanisic, A. E. Barry, and M. F. Good, Escaping the immune system: How the malaria parasite makes vaccine development a challenge, Trends in parasitology, vol.29, pp.612-622, 2013.

R. Stephens and J. Langhorne, Effector memory Th1 CD4 T cells are maintained in a mouse model of chronic malaria, PLoS pathogens, vol.6, p.1001208, 2010.

R. Stephens, B. Seddon, and J. Langhorne, Homeostatic proliferation and IL-7R alpha expression do not correlate with enhanced T cell proliferation and protection in chronic mouse malaria, PloS one, vol.6, p.26686, 2011.

Y. Sterkers, C. Scheidig, M. Da-rocha, C. Lepolard, J. Gysin et al., Members of the low-molecular-mass rhoptry protein complex of Plasmodium falciparum bind to the surface of normal erythrocytes, The Journal of infectious diseases, vol.196, pp.617-621, 2007.

M. M. Stevenson and E. M. Riley, Innate immunity to malaria, Nature reviews. Immunology, vol.4, pp.169-180, 2004.

M. M. Stevenson and M. F. Tam, Differential induction of helper T cell subsets during bloodstage Plasmodium chabaudi AS infection in resistant and susceptible mice, Clinical and experimental immunology, vol.92, pp.77-83, 1993.

M. M. Stevenson, M. F. Tam, S. F. Wolf, and A. Sher, IL-12-induced protection against bloodstage Plasmodium chabaudi AS requires IFN-gamma and TNF-alpha and occurs via a nitric oxide-dependent mechanism, Journal of immunology, vol.155, pp.2545-2556, 1950.

R. J. Stoltzfus, H. M. Chwaya, A. Montresor, M. Albonico, L. Savioli et al., Malaria, hookworms and recent fever are related to anemia and iron status indicators in 0-to 5-y old Zanzibari children and these relationships change with age, The Journal of nutrition, vol.130, pp.1724-1733, 2000.

K. D. Stone, C. Prussin, and D. D. Metcalfe, IgE, mast cells, basophils, and eosinophils, The Journal of allergy and clinical immunology, vol.125, pp.73-80, 2010.

Z. Su and M. M. Stevenson, Central role of endogenous gamma interferon in protective immunity against blood-stage Plasmodium chabaudi AS infection, Infection and immunity, vol.68, pp.4399-4406, 2000.

Z. Su and M. M. Stevenson, IL-12 is required for antibody-mediated protective immunity against blood-stage Plasmodium chabaudi AS malaria infection in mice, Journal of immunology, vol.168, pp.1348-1355, 1950.

A. Suhrbier, L. A. Winger, E. Castellano, and R. E. Sinden, Survival and antigenic profile of irradiated malarial sporozoites in infected liver cells, Infection and immunity, vol.58, pp.2834-2839, 1990.

K. Suzue, T. Asai, T. Takeuchi, and S. Koyasu, In vivo role of IFN-gamma produced by antigen-presenting cells in early host defense against intracellular pathogens, European journal of immunology, vol.33, pp.2666-2675, 2003.

A. Swaika, W. A. Hammond, and R. W. Joseph, Current state of anti-PD-L1 and anti-PD-1 agents in cancer therapy, Molecular immunology, vol.67, pp.4-17, 2015.

K. J. Taylor, T. T. Van, S. M. Macdonald, S. R. Meshnick, R. T. Fernley et al., Immunization of mice with Plasmodium TCTP delays establishment of Plasmodium infection, Parasite immunology, vol.37, pp.23-31, 2015.

A. W. Taylor-robinson, A model of development of acquired immunity to malaria in humans living under endemic conditions, Medical hypotheses, vol.58, pp.148-156, 2002.

A. W. Taylor-robinson and R. S. Phillips, B cells are required for the switch from Th1-to Th2regulated immune responses to Plasmodium chabaudi chabaudi infection, Infection and immunity, vol.62, pp.2490-2498, 1994.

A. W. Taylor-robinson and R. S. Phillips, Infective dose modulates the balance between Th1and Th2-regulated immune responses during blood-stage malaria infection, Scandinavian journal of immunology, vol.48, pp.527-534, 1998.

A. C. Teirlinck, M. B. Mccall, M. Roestenberg, A. Scholzen, R. Woestenenk et al., Longevity and composition of cellular immune responses following experimental Plasmodium falciparum malaria infection in humans, PLoS pathogens, vol.7, p.1002389, 2011.

A. Telerman and R. Amson, The molecular programme of tumour reversion: the steps beyond malignant transformation, Nature reviews. Cancer, vol.9, pp.206-216, 2009.

V. Thathy and R. Menard, Gene targeting in Plasmodium berghei, Methods in molecular medicine, vol.72, pp.317-331, 2002.

P. Thaw, N. J. Baxter, A. M. Hounslow, C. Price, J. P. Waltho et al., Structure of TCTP reveals unexpected relationship with guanine nucleotide-free chaperones, Nature structural biology, vol.8, pp.701-704, 2001.

N. Thawani, M. Tam, and M. M. Stevenson, STAT6-mediated suppression of erythropoiesis in an experimental model of malarial anemia, Haematologica, vol.94, pp.195-204, 2009.

C. Thery, M. Ostrowski, and E. Segura, Membrane vesicles as conveyors of immune responses, Nature reviews. Immunology, vol.9, pp.581-593, 2009.

D. O. Thueson, L. S. Speck, M. A. Lett-brown, and J. A. Grant, Histamine-releasing activity (HRA). I. Production by mitogen-or antigen-stimulated human mononuclear cells, Journal of immunology, vol.123, pp.626-632, 1950.

L. M. Ting, M. Gissot, A. Coppi, P. Sinnis, and K. Kim, Attenuated Plasmodium yoelii lacking purine nucleoside phosphorylase confer protective immunity, Nature medicine, vol.14, pp.954-958, 2008.

A. J. Tormo, M. C. Letellier, M. Sharma, G. Elson, S. Crabe et al., IL-6 activates STAT5 in T cells, Cytokine, vol.60, pp.575-582, 2012.

M. Troye-blomberg, K. Berzins, and P. Perlmann, T-cell control of immunity to the asexual blood stages of the malaria parasite, Critical reviews in immunology, vol.14, pp.131-155, 1994.

M. Troye-blomberg, P. Perlmann, L. Mincheva-nilsson, and H. Perlmann, Immune regulation of protection and pathogenesis in Plasmodium falciparum malaria, Parassitologia, vol.41, pp.131-138, 1999.

M. Troye-blomberg, E. M. Riley, L. Kabilan, M. Holmberg, H. Perlmann et al., Production by activated human T cells of interleukin 4 but not interferon-gamma is associated with elevated levels of serum antibodies to activating malaria antigens, Proceedings of the National Academy of Sciences of the United States of America, vol.87, pp.5484-5488, 1990.

M. Troye-blomberg, S. Worku, P. Tangteerawatana, R. Jamshaid, K. Soderstrom et al., Human gamma delta T cells that inhibit the in vitro growth of the asexual blood stages of the Plasmodium falciparum parasite express cytolytic and proinflammatory molecules, Scandinavian journal of immunology, vol.50, pp.642-650, 1999.

S. W. Tse, A. J. Radtke, and F. Zavala, Induction and maintenance of protective CD8+ T cells against malaria liver stages: implications for vaccine development, Memorias do Instituto Oswaldo Cruz, vol.106, pp.172-178, 2011.

G. Turner, Cerebral malaria. Brain pathology, vol.7, pp.569-582, 1997.

M. Tuynder, G. Fiucci, S. Prieur, A. Lespagnol, A. Geant et al., Translationally controlled tumor protein is a target of tumor reversion, Proceedings of the National Academy of Sciences of the United States of America, vol.101, pp.15364-15369, 2004.

M. Tuynder, L. Susini, S. Prieur, S. Besse, G. Fiucci et al., Biological models and genes of tumor reversion: cellular reprogramming through tpt1/TCTP and SIAH1, Proceedings of the National Academy of Sciences of the United States of America, vol.99, pp.14976-14981, 2002.

B. C. Urban, D. J. Ferguson, A. Pain, N. Willcox, M. Plebanski et al., Plasmodium falciparum-infected erythrocytes modulate the maturation of dendritic cells, Nature, vol.400, pp.73-77, 1999.

M. Vafa, E. Israelsson, B. Maiga, A. Dolo, O. K. Doumbo et al., Relationship between immunoglobulin isotype response to Plasmodium falciparum blood stage antigens and parasitological indexes as well as splenomegaly in sympatric ethnic groups living in Mali, Acta tropica, vol.109, pp.12-16, 2009.

M. Vafa, B. Maiga, K. Berzins, M. Hayano, S. Bereczky et al., Associations between the IL-4-590 T allele and Plasmodium falciparum infection prevalence in asymptomatic Fulani of Mali. Microbes and infection, vol.9, pp.1043-1048, 2007.

N. Van-braeckel-budimir, J. T. Harty-;-van-der-heyde, H. C. , D. Huszar, C. Woodhouse et al., The resolution of acute malaria in a definitive model of B cell deficiency, the JHD mouse, Frontiers in microbiology, vol.5, pp.4557-4562, 1950.

H. C. Van-der-heyde, B. Pepper, J. Batchelder, F. Cigel, and W. P. Weidanz, The time course of selected malarial infections in cytokine-deficient mice, Experimental parasitology, vol.85, pp.206-213, 1997.

T. Van-der-poll, C. V. Keogh, X. Guirao, W. A. Buurman, M. Kopf et al., Interleukin6 gene-deficient mice show impaired defense against pneumococcal pneumonia, The Journal of infectious diseases, vol.176, pp.439-444, 1997.

M. R. Van-dijk, B. Douradinha, B. Franke-fayard, V. Heussler, M. W. Van-dooren et al., Genetically attenuated, P36p-deficient malarial sporozoites induce protective immunity and apoptosis of infected liver cells, Proceedings of the National Academy of Sciences of the United States of America, vol.102, pp.12194-12199, 2005.

J. Vanderberg, R. Nussenzweig, and H. Most, Protective immunity produced by the injection of x-irradiated sporozoites of Plasmodium berghei. V. In vitro effects of immune serum on sporozoites, Military medicine, vol.134, pp.1183-1190, 1969.

F. Verra, G. Luoni, C. Calissano, M. Troye-blomberg, P. Perlmann et al., IL4-589C/T polymorphism and IgE levels in severe malaria, Acta tropica, vol.90, pp.205-209, 2004.

A. Villegas-mendez, R. Greig, T. N. Shaw, J. B. Souza, E. G. Findlay et al., IFN-gammaproducing CD4+ T cells promote experimental cerebral malaria by modulating CD8+ T cell accumulation within the brain, Journal of immunology, vol.189, pp.968-979, 1950.

J. M. Vinetz, S. Kumar, M. F. Good, B. J. Fowlkes, J. A. Berzofsky et al., Adoptive transfer of CD8+ T cells from immune animals does not transfer immunity to blood stage Plasmodium yoelii malaria, Journal of immunology, vol.144, pp.1069-1074, 1950.

T. Von-der-weid, N. Honarvar, and J. Langhorne, Gene-targeted mice lacking B cells are unable to eliminate a blood stage malaria infection, Journal of immunology, vol.156, pp.2510-2516, 1950.

B. M. Vonakis, R. Sora, J. M. Langdon, V. Casolaro, and S. M. Macdonald, Inhibition of cytokine gene transcription by the human recombinant histamine-releasing factor in human T lymphocytes, Journal of immunology, vol.171, pp.3742-3750, 1950.

I. Vouldoukis, D. Mazier, D. Moynet, D. Thiolat, D. Malvy et al., IgE mediates killing of intracellular Toxoplasma gondii by human macrophages through CD23-dependent, interleukin-10 sensitive pathway, PloS one, vol.6, p.18289, 2011.

S. J. Waddell, S. J. Popper, K. H. Rubins, M. J. Griffiths, P. O. Brown et al., Dissecting interferon-induced transcriptional programs in human peripheral blood cells, PloS one, vol.5, p.9753, 2010.

S. Waki, J. Tamura, M. Imanaka, S. Ishikawa, and M. Suzuki, Plasmodium berghei: isolation and maintenance of an irradiation attenuated strain in the nude mouse, Experimental parasitology, vol.53, pp.335-340, 1982.

D. J. Walker, J. L. Pitsch, M. M. Peng, B. L. Robinson, W. Peters et al., Mechanisms of artemisinin resistance in the rodent malaria pathogen Plasmodium yoelii, Antimicrobial agents and chemotherapy, vol.44, pp.344-347, 2000.

R. Wang, J. D. Smith, and S. H. Kappe, Advances and challenges in malaria vaccine development, Expert reviews in molecular medicine, vol.11, p.39, 2009.

P. Ward, L. Equinet, J. Packer, and C. Doerig, Protein kinases of the human malaria parasite Plasmodium falciparum: the kinome of a divergent eukaryote, BMC Genomics, vol.5, p.79, 2004.
URL : https://hal.archives-ouvertes.fr/inserm-00103327

G. E. Weiss, P. D. Crompton, S. Li, L. A. Walsh, S. Moir et al., Atypical memory B cells are greatly expanded in individuals living in a malaria-endemic area, Journal of immunology, vol.183, pp.2176-2182, 1950.

W. R. Weiss, M. Sedegah, R. L. Beaudoin, L. H. Miller, and M. F. Good, CD8+ T cells (cytotoxic/suppressors) are required for protection in mice immunized with malaria sporozoites, Proceedings of the National Academy of Sciences of the United States of America, vol.85, pp.573-576, 1988.

T. Were, G. C. Davenport, J. B. Hittner, C. Ouma, J. M. Vulule et al., Bacteremia in Kenyan children presenting with malaria, Journal of clinical microbiology, vol.49, pp.671-676, 2011.

E. J. Wherry, T cell exhaustion, Nature immunology, vol.12, pp.492-499, 2011.

N. J. White, Assessment of the pharmacodynamic properties of antimalarial drugs in vivo, Antimicrobial agents and chemotherapy, vol.41, pp.1413-1422, 1997.

N. J. White, S. Pukrittayakamee, T. T. Hien, M. A. Faiz, O. A. Mokuolu et al., Malaria. Lancet, vol.383, pp.723-735, 2014.

W. , , 2015.

S. Winkler, M. Willheim, K. Baier, D. Schmid, A. Aichelburg et al., Reciprocal regulation of Th1-and Th2-cytokine-producing T cells during clearance of parasitemia in Plasmodium falciparum malaria, Infection and immunity, vol.66, pp.6040-6044, 1998.

E. A. Winzeler, Malaria research in the post-genomic era, Nature, vol.455, pp.751-756, 2008.

J. J. Winzerling and D. Q. Pham, Iron metabolism in insect disease vectors: mining the Anopheles gambiae translated protein database, Insect biochemistry and molecular biology, vol.36, pp.310-321, 2006.

J. Wipasa, L. Okell, S. Sakkhachornphop, C. Suphavilai, K. Chawansuntati et al., Short-lived IFN-gamma effector responses, but long-lived IL10 memory responses, to malaria in an area of low malaria endemicity, PLoS pathogens, vol.7, p.1001281, 2011.

G. J. Wright and J. C. Rayner, Plasmodium falciparum erythrocyte invasion: combining function with immune evasion, PLoS pathogens, vol.10, p.1003943, 2014.

M. N. Wykes and M. F. Good, What have we learnt from mouse models for the study of malaria?, European journal of immunology, vol.39, pp.2004-2007, 2009.

M. N. Wykes, Y. H. Zhou, X. Q. Liu, and M. F. Good, Plasmodium yoelii can ablate vaccineinduced long-term protection in mice, Journal of immunology, vol.175, pp.2510-2516, 1950.

A. Xu, A. R. Bellamy, and J. A. Taylor, Expression of translationally controlled tumour protein is regulated by calcium at both the transcriptional and post-transcriptional level, The Biochemical journal, vol.342, pp.683-689, 1999.

W. Xu and J. J. Zhang, Stat1-dependent synergistic activation of T-bet for IgG2a production during early stage of B cell activation, Journal of immunology, vol.175, pp.7419-7424, 1950.

D. M. Yanez, D. D. Manning, A. J. Cooley, W. P. Weidanz, and H. C. Van-der-heyde, Participation of lymphocyte subpopulations in the pathogenesis of experimental murine cerebral malaria, Journal of immunology, vol.157, pp.1620-1624, 1950.

F. R. Yarm, Plk phosphorylation regulates the microtubule-stabilizing protein TCTP, Molecular and cellular biology, vol.22, pp.6209-6221, 2002.

S. S. Yazdani, P. Mukherjee, V. S. Chauhan, and C. E. Chitnis, Immune responses to asexual blood-stages of malaria parasites, Current molecular medicine, vol.6, pp.187-203, 2006.

A. M. Yee, H. M. Phan, R. Zuniga, J. E. Salmon, and D. M. Musher, Association between FcgammaRIIa-R131 allotype and bacteremic pneumococcal pneumonia. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, vol.30, pp.25-28, 2000.

T. Yoneto, S. Waki, T. Takai, Y. Tagawa, Y. Iwakura et al., A critical role of Fc receptor-mediated antibody-dependent phagocytosis in the host resistance to blood-stage Plasmodium berghei XAT infection, Journal of immunology, vol.166, pp.6236-6241, 1950.

M. Zhang, C. Fennell, L. Ranford-cartwright, R. Sakthivel, P. Gueirard et al., The Plasmodium eukaryotic initiation factor-2alpha kinase IK2 controls the latency of sporozoites in the mosquito salivary glands, J Exp Med, vol.207, pp.1465-1474, 2010.

J. Zhou, G. Feng, J. Beeson, P. M. Hogarth, S. J. Rogerson et al., CD14(hi)CD16+ monocytes phagocytose antibody-opsonised Plasmodium falciparum infected erythrocytes more efficiently than other monocyte subsets, and require CD16 and complement to do so, BMC medicine, vol.13, p.154, 2015.