滤泡辅助性T细胞在Graves病中的作用:致病机制和治疗意义。

IF 4.2 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Zhengrong Jiang, Linghong Huang, Lijun Chen, Huiyao Cai, Huibin Huang
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引用次数: 0

摘要

Graves病(GD)是一种主要影响甲状腺的特异性自身免疫性疾病,可导致甲状腺毒症,并可能伴有甲状腺外表现,如Graves眼病和胫前黏液水肿。其发病机制涉及自身反应性B细胞的异常增殖,这些细胞随后产生针对促甲状腺激素受体(TSHR)的自身抗体,导致甲状腺激素的过量分泌。辅助性T细胞(Th细胞)在这一过程中起着重要作用。近年来,滤泡辅助性T细胞(Tfh细胞)已被确定为Th细胞的一个新亚群,主要存在于淋巴器官的生发中心(GCs)和外周血中。Tfh细胞促进B细胞的发育和抗体的产生,在GD的发病机制中起着至关重要的作用。它们的异常增殖和功能可能导致自身抗体的产生和组织损伤等病理过程。本文综述了Tfh细胞生物学及其在GD中的作用的最新进展,探讨其作为治疗靶点的潜力,从而为GD的发病机制和治疗提供新的认识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Follicular helper T cells in Graves' disease: pathogenic mechanisms and therapeutic implications.

Graves' disease (GD) is a specific autoimmune disorder that primarily affects the thyroid gland, leading to thyrotoxicosis and potentially accompanied by extrathyroidal manifestations such as Graves' ophthalmopathy and pretibial myxedema. Its pathogenesis involves the abnormal proliferation of autoreactive B cells, which subsequently produce autoantibodies targeting the thyroid-stimulating hormone receptor (TSHR), resulting in excessive secretion of thyroid hormones. Helper T cells (Th cells) play a significant role in this process. In recent years, follicular helper T cells (Tfh cells) have been identified as a novel subset of Th cells, primarily residing in the germinal centers (GCs) of lymphoid organs and in peripheral blood. Tfh cells facilitate B cell development and antibody production, thus playing a crucial role in the pathogenesis of GD. Their aberrant proliferation and function may lead to the production of autoantibodies and pathological processes such as tissue damage. This review summarizes the latest advancements in the biology of Tfh cells and their role in GD, exploring their potential as therapeutic targets, thereby providing new insights into the pathogenesis and treatment of GD.

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来源期刊
CiteScore
9.80
自引率
0.00%
发文量
98
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Endocrinology and Metabolism publishes original, mechanistic studies on the physiology of endocrine and metabolic systems. Physiological, cellular, and molecular studies in whole animals or humans will be considered. Specific themes include, but are not limited to, mechanisms of hormone and growth factor action; hormonal and nutritional regulation of metabolism, inflammation, microbiome and energy balance; integrative organ cross talk; paracrine and autocrine control of endocrine cells; function and activation of hormone receptors; endocrine or metabolic control of channels, transporters, and membrane function; temporal analysis of hormone secretion and metabolism; and mathematical/kinetic modeling of metabolism. Novel molecular, immunological, or biophysical studies of hormone action are also welcome.
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