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辅助性 T 细胞 17 在类风湿关节炎中的致病机制和可塑性。

Th17 cell pathogenicity and plasticity in rheumatoid arthritis.

机构信息

Jiangsu Key Laboratory for Pharmacology and Safety Evaluation of Chinese Materia Medica, School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, Jiangsu Province, People's Republic of China.

出版信息

J Leukoc Biol. 2019 Dec;106(6):1233-1240. doi: 10.1002/JLB.4RU0619-197R. Epub 2019 Sep 9.

Abstract

CD4 Th cells play an important role in the development of rheumatoid arthritis (RA) by regulating adaptive immune response. As major subsets of CD4 Th cells, Th17 cells can produce a large number of hallmark cytokines such as IL-17A and IL-17F, which participate in host defense and immune homeostasis. However, increasing researches have shown that Th17 cells are unstable and exhibit a certain degree of plasticity, which aggravates their pathogenicity. Furthermore, the plasticity and pathogenicity of Th17 cells are closely related with the disease activity in RA. In this paper, the characteristics including phenotype, differentiation, plasticity, and pathogenicity of Th17 cells in RA will be systematically summarized. This will contribute to clarify the immunologic mechanism of RA and further provide a novel strategy for the clinical treatment of autoimmune diseases.

摘要

CD4+T 细胞通过调节适应性免疫反应在类风湿关节炎(RA)的发生发展中发挥重要作用。Th17 细胞作为 CD4+T 细胞的主要亚群之一,能够产生大量特征性细胞因子,如 IL-17A 和 IL-17F,参与宿主防御和免疫稳态。然而,越来越多的研究表明,Th17 细胞不稳定,表现出一定程度的可塑性,从而加重其致病性。此外,Th17 细胞的可塑性和致病性与 RA 的疾病活动密切相关。本文将对 RA 中 Th17 细胞的表型、分化、可塑性和致病性进行系统总结,这将有助于阐明 RA 的免疫机制,并为自身免疫性疾病的临床治疗提供新策略。

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