Genetic Diversity and Protective Efficacy of the RTS,S/AS01 Malaria Vaccine

Daniel E. Neafsey(Broad Institute), Michal Juraska(Cape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa), Trevor Bedford(Cape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa), David Benkeser(Cape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa), Clarissa Valim(Broad Institute), Allison Griggs(Broad Institute), Marc Lievens(GlaxoSmithKline (Belgium)), Salim Abdulla(Ifakara Health Institute), Samuel Adjei(Kwame Nkrumah University of Science and Technology), Tsiri Agbenyega(Kwame Nkrumah University of Science and Technology), Sélidji Todagbé Agnandji(Albert Schweitzer Hospital), Pedro Aíde(Manhiça Health Research Centre), Scott Anderson(Broad Institute), Daniel Ansong(Albert Schweitzer Hospital), John J. Aponte(Manhiça Health Research Centre), Kwaku Poku Asante(Kintampo Health Research Centre), Philip Bejon(Wellcome Trust), Ashley J. Birkett(U.S. President's Malaria Initiative), Myriam Bruls(GlaxoSmithKline (Belgium)), Kristen M. Connolly(Broad Institute), Umberto D’Alessandro(MRC Unit the Gambia), Carlota Dobaño(Manhiça Health Research Centre), Samwel Gesase(National Institute for Medical Research), Brian Greenwood(London School of Hygiene & Tropical Medicine), Jonna Grimsby(Broad Institute), Halidou Tinto(Institut de Recherche en Sciences de la Santé), Mary J. Hamel(AID Atlanta), Irving Hoffman(Communities In Schools of Orange County), Portia Kamthunzi, Simon Kariuki(Kenya Medical Research Institute), Peter G. Kremsner(Albert Schweitzer Hospital), Amanda Leach(GlaxoSmithKline (Belgium)), Bertrand Lell(Albert Schweitzer Hospital), Niall J. Lennon(Broad Institute), John Lusingu(National Institute for Medical Research), Kevin Marsh(Wellcome Trust), Francis Martinson, Jackson T. Molel(Ifakara Health Institute), Eli L. Moss(Broad Institute), Patricia Njuguna(Wellcome Trust), Christian F. Ockenhouse(U.S. President's Malaria Initiative), Bernhards Ogutu, Walter Otieno, Lucas Otieno, Kephas Otieno(Kenya Medical Research Institute), Seth Owusu‐Agyei(Kintampo Health Research Centre), Daniel J. Park(Broad Institute), Karell G. Pellé(Broad Institute), Dana Robbins(Broad Institute), Carsten Russ(Broad Institute), Elizabeth M. Ryan(Broad Institute), Jahit Sacarlal(Manhiça Health Research Centre), Brian Sogoloff(Broad Institute), Hermann Sorgho(Institut de Recherche en Sciences de la Santé), Marcel Tanner(Swiss Tropical and Public Health Institute), Thor G. Theander(University of Copenhagen), Innocent Valéa(Institut de Recherche en Sciences de la Santé), Sarah K. Volkman(Broad Institute), Qing Yu(Broad Institute), Didier Lapierre(GlaxoSmithKline (Belgium)), Bruce W. Birren(Broad Institute), Peter B. Gilbert(Cape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa), Dyann F. Wirth(Harvard University)
New England Journal of Medicine
October 21, 2015
Cited by 450Open Access
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Abstract

BACKGROUND: The RTS,S/AS01 vaccine targets the circumsporozoite protein of Plasmodium falciparum and has partial protective efficacy against clinical and severe malaria disease in infants and children. We investigated whether the vaccine efficacy was specific to certain parasite genotypes at the circumsporozoite protein locus. METHODS: We used polymerase chain reaction-based next-generation sequencing of DNA extracted from samples from 4985 participants to survey circumsporozoite protein polymorphisms. We evaluated the effect that polymorphic positions and haplotypic regions within the circumsporozoite protein had on vaccine efficacy against first episodes of clinical malaria within 1 year after vaccination. RESULTS: In the per-protocol group of 4577 RTS,S/AS01-vaccinated participants and 2335 control-vaccinated participants who were 5 to 17 months of age, the 1-year cumulative vaccine efficacy was 50.3% (95% confidence interval [CI], 34.6 to 62.3) against clinical malaria in which parasites matched the vaccine in the entire circumsporozoite protein C-terminal (139 infections), as compared with 33.4% (95% CI, 29.3 to 37.2) against mismatched malaria (1951 infections) (P=0.04 for differential vaccine efficacy). The vaccine efficacy based on the hazard ratio was 62.7% (95% CI, 51.6 to 71.3) against matched infections versus 54.2% (95% CI, 49.9 to 58.1) against mismatched infections (P=0.06). In the group of infants 6 to 12 weeks of age, there was no evidence of differential allele-specific vaccine efficacy. CONCLUSIONS: These results suggest that among children 5 to 17 months of age, the RTS,S vaccine has greater activity against malaria parasites with the matched circumsporozoite protein allele than against mismatched malaria. The overall vaccine efficacy in this age category will depend on the proportion of matched alleles in the local parasite population; in this trial, less than 10% of parasites had matched alleles. (Funded by the National Institutes of Health and others.).


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