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Potential functions of atypical memory B cells in Plasmodium-exposed individuals

Naturally acquired immunity against clinical malaria is slow to develop, taking years of repeated exposure to parasites to acquire sufficiently broad and potent antibody responses. Increasing evidence suggests that Plasmodium infection and the resulting immune stimulation contribute to changes in th...

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Detalles Bibliográficos
Autores principales: Braddom, Ashley E., Batugedara, Gayani, Bol, Sebastiaan, Bunnik, Evelien M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7666103/
https://www.ncbi.nlm.nih.gov/pubmed/32987039
http://dx.doi.org/10.1016/j.ijpara.2020.08.003
Descripción
Sumario:Naturally acquired immunity against clinical malaria is slow to develop, taking years of repeated exposure to parasites to acquire sufficiently broad and potent antibody responses. Increasing evidence suggests that Plasmodium infection and the resulting immune stimulation contribute to changes in the B cell compartment. In particular, accumulation of atypical memory B cells (atMBCs) is common in Plasmodium-exposed individuals. Similarities to B cell subsets present in other acute and chronic disease settings have provided insight into the development and potential function of these cells; however, their contribution to protection against malaria is still poorly understood. Here, we discuss recent findings that have increased our understanding of atMBCs and outline outstanding questions related to their function and development in the protective immune response to malaria.