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肠道黏膜 IgA B 细胞应答的调节:最新进展。

The regulation of gut mucosal IgA B-cell responses: recent developments.

机构信息

Department of Microbiology and Immunology, Mucosal Immunobiology and Vaccine Center, Institute of Biomedicine, University of Gothenburg, Gothenburg, Sweden.

出版信息

Mucosal Immunol. 2017 Nov;10(6):1361-1374. doi: 10.1038/mi.2017.62. Epub 2017 Jul 26.

Abstract

The majority of activated B cells differentiate into IgA plasma cells, with the gut being the largest producer of immunoglobulin in the body. Secretory IgA antibodies have numerous critical functions of which protection against infections and the role for establishing a healthy microbiota appear most important. Expanding our knowledge of the regulation of IgA B-cell responses and how effective mucosal vaccines can be designed are of critical importance. Here we discuss recent developments in the field that shed light on the uniqueness and complexity of mucosal IgA responses and the control of protective IgA responses in the gut, specifically.

摘要

大多数活化的 B 细胞分化为 IgA 浆细胞,而肠道是体内产生免疫球蛋白的最大器官。分泌型 IgA 抗体具有许多关键功能,其中预防感染和建立健康微生物群的作用似乎最为重要。扩大我们对 IgA B 细胞反应的调节以及如何设计有效的黏膜疫苗的认识至关重要。在这里,我们讨论了该领域的最新进展,这些进展揭示了黏膜 IgA 反应的独特性和复杂性,以及对肠道中保护性 IgA 反应的控制。

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