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调节性 B 细胞的免疫抑制机制。

Immunosuppressive Mechanisms of Regulatory B Cells.

机构信息

Programa Disciplinario de Inmunología, Facultad de Medicina, Instituto de Ciencias Biomédicas (ICBM), Universidad de Chile, Santiago, Chile.

Instituto Milenio en Inmunología e Inmunoterapia, Santiago, Chile.

出版信息

Front Immunol. 2021 Apr 29;12:611795. doi: 10.3389/fimmu.2021.611795. eCollection 2021.

DOI:10.3389/fimmu.2021.611795
PMID:33995344
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8118522/
Abstract

Regulatory B cells (Bregs) is a term that encompasses all B cells that act to suppress immune responses. Bregs contribute to the maintenance of tolerance, limiting ongoing immune responses and reestablishing immune homeostasis. The important role of Bregs in restraining the pathology associated with exacerbated inflammatory responses in autoimmunity and graft rejection has been consistently demonstrated, while more recent studies have suggested a role for this population in other immune-related conditions, such as infections, allergy, cancer, and chronic metabolic diseases. Initial studies identified IL-10 as the hallmark of Breg function; nevertheless, the past decade has seen the discovery of other molecules utilized by human and murine B cells to regulate immune responses. This new arsenal includes other anti-inflammatory cytokines such IL-35 and TGF-β, as well as cell surface proteins like CD1d and PD-L1. In this review, we examine the main suppressive mechanisms employed by these novel Breg populations. We also discuss recent evidence that helps to unravel previously unknown aspects of the phenotype, development, activation, and function of IL-10-producing Bregs, incorporating an overview on those questions that remain obscure.

摘要

调节性 B 细胞(Bregs)是一个术语,它包括所有具有抑制免疫反应作用的 B 细胞。Bregs 有助于维持耐受,限制持续的免疫反应并重建免疫稳态。Bregs 在抑制自身免疫和移植物排斥中与炎症反应过度相关的病理学方面发挥着重要作用,这一点已得到一致证明,而最近的研究表明,该群体在其他与免疫相关的疾病中也具有作用,如感染、过敏、癌症和慢性代谢疾病。最初的研究确定了 IL-10 是 Breg 功能的标志;然而,在过去的十年中,人们发现了人类和鼠类 B 细胞用于调节免疫反应的其他分子。这个新的“武器库”包括其他抗炎细胞因子,如 IL-35 和 TGF-β,以及细胞表面蛋白,如 CD1d 和 PD-L1。在这篇综述中,我们研究了这些新型 Breg 群体所采用的主要抑制机制。我们还讨论了最近的证据,这些证据有助于揭示 IL-10 产生 Bregs 的表型、发育、激活和功能的以前未知方面,包括对那些仍不清楚的问题的概述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ef6/8118522/eca7b20281b6/fimmu-12-611795-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ef6/8118522/61ad2f871213/fimmu-12-611795-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ef6/8118522/e6a4ee7a1367/fimmu-12-611795-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ef6/8118522/eca7b20281b6/fimmu-12-611795-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ef6/8118522/61ad2f871213/fimmu-12-611795-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ef6/8118522/e6a4ee7a1367/fimmu-12-611795-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ef6/8118522/eca7b20281b6/fimmu-12-611795-g0003.jpg

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