Authors
Ja-Hyun Koo, Prabhanshu Tripathi, Yevel Flores-Garcia, Kazutoyo Miura, Ganchimeg Bayarsaikhan, Chen-Hsiang Shen, Stephanie R Weldon, Sven Kratochvil, Thavaleak Prum, Ali A Albowaidey, Ye-Ji Kim, Jordan R Ellis-Pugh, Quynh Anh Phan, Jennifer Suurbaar, Robert Sifa Onjiko, Misook Choe, Gordon A Dale, Haotian Lei, Nicholas C Morano, Lais Da Silva Pereira, Marlon Dillon, Michael F Bender, Mariah Lofgren, Baoshan Zhang, Theodore C Pierson, Lawrence Shapiro, Tongqing Zhou, Usha Nair, Azza H Idris, Fidel Zavala, Peter D Kwong, Robert A Seder, Facundo D Batista
Published in
The Journal of experimental medicine. Volume 223. Issue 9. Sep 07, 2026. Epub Aug 07, 2026.
Abstract
The first approval of malaria vaccines RTS,S/AS01 and R21/Matrix M marked a major milestone. Both vaccines present a portion of the Plasmodium falciparum circumsporozoite protein (PfCSP) containing an immunodominant major repeat region, which may limit breadth to other protective epitopes, limiting efficacy and durability. Using B cell receptor (BCR) knock-in mice, we found that the R21-included PfCSP epitope elicited robust B cell responses to the immunodominant major repeats but not to other highly protective epitopes, the minor repeat and junction. We then defined a minimal peptide capable of eliciting minor repeat-specific B cell responses and generating highly protective antibodies (Abs). We characterized these Abs bioinformatically and structurally to identify protective traits, which informed the design of variant Abs with improved affinity. Finally, we demonstrated that vaccination combining the R21-included PfCSP epitope, the minimal minor repeat peptide, and a junctional region immunogen elicited balanced B cell and Ab responses, enhancing protection in vivo. Broadening responses through immunofocusing may overcome immunogenic gaps in current malaria vaccines.
PMID:
42565808
Bibliographic data and abstract were imported from PubMed on 07 Aug 2026.
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