TY - JOUR
T1 - Breadth of humoral response and antigenic targets of sporozoite-inhibitory antibodies associated with sterile protection induced by controlled human malaria infection
AU - Peng, Kaitian
AU - Goh, Yun Shan
AU - Siau, Anthony
AU - Franetich, Jean François
AU - Chia, Wan Ni
AU - Ong, Alice Soh Meoy
AU - Malleret, Benoit
AU - Wu, Ying Ying
AU - Snounou, Georges
AU - Hermsen, Cornelus C.
AU - Adams, John H.
AU - Mazier, Dominique
AU - Preiser, Peter R.
AU - Sauerwein, Robert W.
AU - Grüner, Anne Charlotte
AU - Rénia, Laurent
N1 - Publisher Copyright:
© 2016 John Wiley & Sons Ltd
PY - 2016/12/1
Y1 - 2016/12/1
N2 - The development of an effective malaria vaccine has remained elusive even until today. This is because of our incomplete understanding of the immune mechanisms that confer and/or correlate with protection. Human volunteers have been protected experimentally from a subsequent challenge by immunization with Plasmodium falciparum sporozoites under drug cover. Here, we demonstrate that sera from the protected individuals contain neutralizing antibodies against the pre-erythrocytic stage. To identify the antigen(s) recognized by these antibodies, a newly developed library of P. falciparum antigens was screened with the neutralizing sera. Antibodies from protected individuals recognized a broad antigenic repertoire of which three antigens, PfMAEBL, PfTRAP and PfSEA1 were recognized by most protected individuals. As a proof of principle, we demonstrated that anti-PfMAEBL antibodies block liver stage development in human hepatocytes. Thus, these antigens identified are promising targets for vaccine development against malaria.
AB - The development of an effective malaria vaccine has remained elusive even until today. This is because of our incomplete understanding of the immune mechanisms that confer and/or correlate with protection. Human volunteers have been protected experimentally from a subsequent challenge by immunization with Plasmodium falciparum sporozoites under drug cover. Here, we demonstrate that sera from the protected individuals contain neutralizing antibodies against the pre-erythrocytic stage. To identify the antigen(s) recognized by these antibodies, a newly developed library of P. falciparum antigens was screened with the neutralizing sera. Antibodies from protected individuals recognized a broad antigenic repertoire of which three antigens, PfMAEBL, PfTRAP and PfSEA1 were recognized by most protected individuals. As a proof of principle, we demonstrated that anti-PfMAEBL antibodies block liver stage development in human hepatocytes. Thus, these antigens identified are promising targets for vaccine development against malaria.
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U2 - 10.1111/cmi.12608
DO - 10.1111/cmi.12608
M3 - Article
C2 - 27130708
AN - SCOPUS:84971277140
SN - 1462-5814
VL - 18
SP - 1739
EP - 1750
JO - Cellular Microbiology
JF - Cellular Microbiology
IS - 12
ER -