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滤泡调节性固有淋巴细胞群损害生发中心 Tfh 细胞与 B 细胞之间的相互作用。

A follicular regulatory Innate Lymphoid Cell population impairs interactions between germinal center Tfh and B cells.

机构信息

The Department of Medicine, Division of Infectious Diseases & HIV Medicine, Drexel University College of Medicine, Philadelphia, PA, USA.

The Department of Molecular and Cellular Biology and Genetics, Drexel University College of Medicine, Philadelphia, PA, USA.

出版信息

Commun Biol. 2021 May 12;4(1):563. doi: 10.1038/s42003-021-02079-0.

Abstract

Innate Lymphoid Cells (ILCs) are immune cells typically found on mucosal surfaces and in secondary lymphoid organs where they regulate the immune response to pathogens. Despite their key role in the immune response, there are still fundamental gaps in our understanding of ILCs. Here we report a human ILC population present in the follicles of tonsils and lymph nodes termed follicular regulatory ILCs (ILC) that to our knowledge has not been previously identified. ILC have a distinct phenotype and transcriptional program when compared to other defined ILCs. Surprisingly, ILC inhibit the ability of follicular helper T (Tfh) cells to provide B cell help. The localization of ILC to the germinal centers suggests these cells may interfere with germinal center B cell (GC-B) and germinal center Tfh cell (GC-Tfh) interactions through the production of transforming growth factor beta (TGF-β. Intriguingly, under conditions of impaired GC-Tfh-GC-B cell interactions, such as human immunodeficiency virus (HIV) infection, the frequency of these cells is increased. Overall, we predict a role for ILC in regulating GC-Tfh-GC-B cell interactions and propose they expand in chronic inflammatory conditions.

摘要

固有淋巴细胞 (ILC) 是通常存在于黏膜表面和次级淋巴器官中的免疫细胞,它们调节对病原体的免疫反应。尽管它们在免疫反应中起着关键作用,但我们对 ILC 的理解仍存在基本的差距。在这里,我们报告了一种存在于扁桃体和淋巴结滤泡中的人类 ILC 群体,称为滤泡调节性 ILC (ILC),据我们所知,这种细胞以前尚未被识别。与其他已定义的 ILC 相比,ILC 具有独特的表型和转录程序。令人惊讶的是,ILC 抑制滤泡辅助 T (Tfh) 细胞提供 B 细胞帮助的能力。ILC 定位于生发中心表明这些细胞可能通过产生转化生长因子β (TGF-β) 干扰生发中心 B 细胞 (GC-B) 和生发中心 Tfh 细胞 (GC-Tfh) 之间的相互作用。有趣的是,在 GC-Tfh-GC-B 细胞相互作用受损的情况下,例如人类免疫缺陷病毒 (HIV) 感染,这些细胞的频率增加。总的来说,我们预测 ILC 在调节 GC-Tfh-GC-B 细胞相互作用中起作用,并提出它们在慢性炎症条件下扩张。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5814/8115650/f6c8f377ab4a/42003_2021_2079_Fig1_HTML.jpg

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