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系统性硬化症中异常的B淋巴细胞激活与功能

Abnormal B lymphocyte activation and function in systemic sclerosis.

作者信息

Yoshizaki Ayumi, Sato Shinichi

机构信息

Department of Dermatology, University of Tokyo Graduate School of Medicine, Tokyo, Japan.

出版信息

Ann Dermatol. 2015 Feb;27(1):1-9. doi: 10.5021/ad.2015.27.1.1. Epub 2015 Feb 3.

Abstract

Systemic sclerosis (SSc) is characterized by tissue fibrosis and autoimmunity. Although the pathogenic relationship between autoimmunity and clinical manifestations of SSc remains unknown, SSc patients display abnormal immune responses including the production of disease-specific autoantibodies. Previous studies have demonstrated that B cells play a critical role in systemic autoimmunity and disease expression through various functions such as induction of the activation of other immune cells in addition to autoantibody production. CD19 is a crucial regulator of B cell activation. Recent studies demonstrated that B cells from SSc patients showed an up-regulated CD19 signaling pathway that induced SSc-specific autoantibody production in SSc mouse models. CD19 transgenic mice lost tolerance for autoantigen and generated autoantibodies spontaneously. B cells from SSc patients exhibited an overexpression of CD19 that induced SSc-specific autoantibody production in transgenic mice. Moreover, SSc patients displayed intrinsic B cell abnormalities characterized by chronic hyper-reactivity of memory B cells, which was possibly due to CD19 overexpression. Similarly, B cells from a tight-skin mouse, a genetic model of SSc, showed augmented CD19 signaling. In bleomycin-induced SSc mouse models, endogenous ligands for toll-like receptor 4 induced by bleomycin stimulated B cells to produce various fibrogenic cytokines and autoantibodies. Remarkably, the loss of CD19 resulted in the inhibition of B cell hyper-reactivity and autoantibody production, which are associated with improvements in fibrosis and a parallel decrease in fibrogenic cytokine production by B cells. Taken together, the findings suggest that altered B cell function may result in tissue fibrosis as well as autoimmunity in SSc.

摘要

系统性硬化症(SSc)的特征是组织纤维化和自身免疫。尽管自身免疫与SSc临床表现之间的致病关系尚不清楚,但SSc患者表现出异常的免疫反应,包括产生疾病特异性自身抗体。先前的研究表明,B细胞通过多种功能在系统性自身免疫和疾病表达中起关键作用,除了产生自身抗体外,还可诱导其他免疫细胞的激活。CD19是B细胞激活的关键调节因子。最近的研究表明,SSc患者的B细胞显示CD19信号通路上调,这在SSc小鼠模型中诱导了SSc特异性自身抗体的产生。CD19转基因小鼠对自身抗原失去耐受性并自发产生自身抗体。SSc患者的B细胞表现出CD19的过表达,这在转基因小鼠中诱导了SSc特异性自身抗体的产生。此外,SSc患者表现出内在的B细胞异常,其特征是记忆B细胞的慢性高反应性,这可能是由于CD19过表达所致。同样,来自SSc基因模型紧皮小鼠的B细胞显示CD19信号增强。在博来霉素诱导的SSc小鼠模型中,博来霉素诱导的Toll样受体4内源性配体刺激B细胞产生各种促纤维化细胞因子和自身抗体。值得注意的是,CD19的缺失导致B细胞高反应性和自身抗体产生受到抑制,这与纤维化的改善以及B细胞促纤维化细胞因子产生的平行减少有关。综上所述,这些发现表明B细胞功能改变可能导致SSc中的组织纤维化以及自身免疫。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8016/4323585/4ad1cb451395/ad-27-1-g001.jpg

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