Human responses to the DNA prime/chimpanzee adenovirus (ChAd63) boost vaccine identify CSP, AMA1 and TRAP MHC Class I-restricted epitopes

This integrated approach using immunoassays and bioinformatics identified and confirmed AMA1-MHC Class I-restricted epitopes and a list of predicted additional epitopes which could be evaluated in future studies to assess possible association with protection against CHMI in the Phase 1 trial participants. The results suggest that identification of protection-associated epitopes within malaria antigens is feasible and can help design potent next generation multi-antigen, multi-epitope malaria vaccines for a genetically diverse population and to develop robust assays to measure protective cellular immunity against pre-erythrocytic stages of malaria. This approach can be used to develop vaccines for other novel emerging infectious disease pathogens.

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Publication Details

Journal
PLoS ONE
Published
2025-02-13
DOI
https://doi.org/10.1371/journal.pone.0318098
Citations
2
Primary Topic
vaccines and immunoinformatics approaches
Type
article
Field-Weighted Citation Impact
1.61

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article

Human responses to the DNA prime/chimpanzee adenovirus (ChAd63) boost vaccine identify CSP, AMA1 and TRAP MHC Class I-restricted epitopes

Lorraine Soisson, Martha Sedegah, Christopher Duplessis, Noelle B. Patterson et al.
2 citations
PLoS ONE
vaccines and immunoinformatics approaches
1.61
article

Human responses to the DNA prime/chimpanzee adenovirus (ChAd63) boost vaccine identify CSP, AMA1 and TRAP MHC Class I-restricted epitopes

Lorraine Soisson, Martha Sedegah, Christopher Duplessis, Noelle B. Patterson, Rachel Velasco, Arnel Belmonte, Bjoern Peters, Marvin J. Sklar, María Belmonte, Keith Limbach, Sandra Inoue, Judith E. Epstein, Jun Huang, Kimberly A. Edgel, Michael R. Hollingdale, Santina Maiolatesi, Eileen Villasante, Harini Ganeshan
article en
2 citations

Abstract

This integrated approach using immunoassays and bioinformatics identified and confirmed AMA1-MHC Class I-restricted epitopes and a list of predicted additional epitopes which could be evaluated in future studies to assess possible association with protection against CHMI in the Phase 1 trial participants. The results suggest that identification of protection-associated epitopes within malaria antigens is feasible and can help design potent next generation multi-antigen, multi-epitope malaria vaccines for a genetically diverse population and to develop robust assays to measure protective cellular immunity against pre-erythrocytic stages of malaria. This approach can be used to develop vaccines for other novel emerging infectious disease pathogens.

PLoS ONEVol. 20(2)
Henry M. Jackson Foundation (US), National Institutes of Health (US), La Jolla Institute for Immunology (US), Naval Medical Research Command (US), General Dynamics (United States) (US), United States Agency for International Development (US), National Institute of Allergy and Infectious Diseases (US)
U.S. Department of Defense, United States Agency for International Development, Henry M. Jackson Foundation, National Institutes of Health, U.S. Navy, National Medical Research Council, National Institute of Allergy and Infectious Diseases
Good health and well-being
Openalex Percentile: Top 19%
vaccines and immunoinformatics approaches
1.61
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