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多阶段保护型抗 CelTOS 单克隆抗体,对疟疾具有跨物种的无菌保护作用。

Multistage protective anti-CelTOS monoclonal antibodies with cross-species sterile protection against malaria.

机构信息

Host‒Pathogen Interactions and Structural Vaccinology Section, Laboratory of Malaria Immunology and Vaccinology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.

Center of Global Health and Interdisciplinary Research, College of Public Health, University of South Florida, Tampa, FL, USA.

出版信息

Nat Commun. 2024 Aug 29;15(1):7487. doi: 10.1038/s41467-024-51701-2.

Abstract

CelTOS is a malaria vaccine antigen that is conserved in Plasmodium and other apicomplexan parasites and plays a role in cell-traversal. The structural basis and mechanisms of CelTOS-induced protective immunity to parasites are unknown. Here, CelTOS-specific monoclonal antibodies (mAbs) 7g7 and 4h12 demonstrated multistage activity, protecting against liver infection and preventing parasite transmission to mosquitoes. Both mAbs demonstrated cross-species activity with sterile protection against in vivo challenge with transgenic parasites containing either P. falciparum or P. vivax CelTOS, and with transmission reducing activity against P. falciparum. The mAbs prevented CelTOS-mediated pore formation providing insight into the protective mechanisms. X-ray crystallography and mutant-library epitope mapping revealed two distinct broadly conserved neutralizing epitopes. 7g7 bound to a parallel dimer of CelTOS, while 4h12 bound to a novel antiparallel dimer architecture. These findings inform the design of antibody therapies and vaccines and raise the prospect of a single intervention to simultaneously combat P. falciparum and P. vivax malaria.

摘要

CelTOS 是一种疟原虫疫苗抗原,在疟原虫和其他顶复门寄生虫中保守,在细胞穿入中发挥作用。CelTOS 诱导寄生虫保护性免疫的结构基础和机制尚不清楚。在这里,CelTOS 特异性单克隆抗体 (mAb) 7g7 和 4h12 表现出多阶段活性,可预防肝脏感染并防止寄生虫传播给蚊子。这两种 mAb 表现出种间活性,对含有疟原虫或间日疟原虫 CelTOS 的转基因寄生虫的体内挑战具有无菌保护作用,并具有降低疟原虫传播的活性。该 mAb 可阻止 CelTOS 介导的孔形成,从而深入了解保护机制。X 射线晶体学和突变文库表位作图揭示了两个截然不同的广泛保守中和表位。7g7 结合 CelTOS 的平行二聚体,而 4h12 结合新型反平行二聚体结构。这些发现为抗体治疗和疫苗的设计提供了信息,并提出了一种单一干预措施同时对抗疟原虫和间日疟原虫疟疾的前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e50f/11362571/39f6106a2549/41467_2024_51701_Fig1_HTML.jpg

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