环子孢子蛋白
表位
病毒学
单克隆抗体
恶性疟原虫
疟疾
生物
抗体
抗原
免疫学
作者
Cherrelle Dacon,Re’em Moskovitz,Kristian E. Swearingen,Lais Da Silva Pereira,Yevel Flores-García,Maya Aleshnick,Sachie Kanatani,Barbara J. Flynn,Alvaro Molina-Cruz,Kurt Wollenberg,Maria Traver,Payton Kirtley,Lauren Purser,Marlon Dillon,Brian Bonilla,Adriano Franco,Sirak Petros,Jake E. Kritzberg,Courtney Tucker,Gonzalo E. González‐Páez
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2025-01-02
卷期号:387 (6729): eadr0510-eadr0510
被引量:13
标识
DOI:10.1126/science.adr0510
摘要
The most advanced monoclonal antibodies (mAbs) and vaccines against malaria target the central repeat region or closely related sequences within the Plasmodium falciparum circumsporozoite protein (PfCSP). Here, using an antigen-agnostic strategy to investigate human antibody responses to whole sporozoites, we identified a class of mAbs that target a cryptic PfCSP epitope that is only exposed after cleavage and subsequent pyroglutamylation (pGlu) of the newly formed N terminus. This pGlu-CSP epitope is not targeted by current anti-PfCSP mAbs and is not included in the licensed malaria vaccines. MAD21-101, the most potent mAb in this class, confers sterile protection against Pf infection in a human liver–chimeric mouse model. These findings reveal a site of vulnerability on the sporozoite surface that can be targeted by next-generation antimalarial interventions.
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