Regulation of B Cell Responses in SLE by Three Classes of Interferons.

Regulation of B Cell Responses in SLE by Three Classes of Interferons.
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通过三类干扰素调节SLE中B细胞反应的调节。

DOI:
10.3390/ijms221910464
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发表时间:
2021-09-28
影响因子:
5.6
通讯作者:
Rahman ZSM
Rahman ZSM
中科院分区:
生物学2区
文献类型:
--
作者:
Domeier PP;Rahman ZSM

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有三种类型的干扰素(1型,2型和3型)可以促进各种自身免疫性疾病的发展和维持,包括系统性红斑狼疮(SLE)。每一类干扰素通过不同的信号传导机制促进自身反应性B细胞和SLE相关自身抗体的产生。SLE患者接受不同的1型干扰素阻断生物制剂治疗有不同的结果,这表明其他环境和遗传因素可能决定了这些细胞因子如何促进自身反应性B细胞和SLE的发展。了解每类干扰素如何控制SLE中的B细胞应答对于开发优化的B细胞和干扰素靶向治疗是必要的。在这篇综述中,我们将讨论各类干扰素如何差异促进外周B细胞耐受性的丧失,并导致自身反应性B细胞,自身抗体和SLE的发展。
There are three classes of interferons (type 1, 2, and 3) that can contribute to the development and maintenance of various autoimmune diseases, including systemic lupus erythematosus (SLE). Each class of interferons promotes the generation of autoreactive B cells and SLE-associated autoantibodies by distinct signaling mechanisms. SLE patients treated with various type 1 interferon-blocking biologics have diverse outcomes, suggesting that additional environmental and genetic factors may dictate how these cytokines contribute to the development of autoreactive B cells and SLE. Understanding how each class of interferons controls B cell responses in SLE is necessary for developing optimized B cell- and interferon-targeted therapeutics. In this review, we will discuss how each class of interferons differentially promotes the loss of peripheral B cell tolerance and leads to the development of autoreactive B cells, autoantibodies, and SLE.
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