调节性B细胞
免疫系统
免疫学
自身免疫
生物
白细胞介素10
人口
B细胞
调节性T细胞
炎症
T细胞
细胞生物学
幼稚B细胞
B-1电池
B细胞受体
FOXP3型
生发中心
抗原
白细胞介素2受体
免疫耐受
医学
环境卫生
作者
Diego Catalán,Miguel Andrés Mansilla,Ashley Ferrier,Lilian Soto,Kristīne Oļeiņika,Juan Carlos Aguillón,Octavio Aravena
标识
DOI:10.3389/fimmu.2021.611795
摘要
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.
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