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miRNAs 改变辅助性 T 细胞 17 细胞在自身免疫性疾病发病机制中的命运。

miRNAs Alter T Helper 17 Cell Fate in the Pathogenesis of Autoimmune Diseases.

机构信息

Department of Dermatology, Zhongshan Hospital, Fudan University, Shanghai, China.

出版信息

Front Immunol. 2021 Apr 21;12:593473. doi: 10.3389/fimmu.2021.593473. eCollection 2021.

Abstract

T helper 17 (Th17) cells are characterized by the secretion of the IL-17 cytokine and are essential for the immune response against bacterial and fungal infections. Despite the beneficial roles of Th17 cells, unrestrained IL-17 production can contribute to immunopathology and inflammatory autoimmune diseases, including multiple sclerosis, rheumatoid arthritis, and inflammatory bowel disease. Although these diverse outcomes are directed by the activation of Th17 cells, the regulation of Th17 cells is incompletely understood. The discovery that microRNAs (miRNAs) are involved in the regulation of Th17 cell differentiation and function has greatly improved our understanding of Th17 cells in immune response and disease. Here, we provide an overview of the biogenesis and function of miRNA and summarize the role of miRNAs in Th17 cell differentiation and function. Finally, we focus on recent advances in miRNA-mediated dysregulation of Th17 cell fate in autoimmune diseases.

摘要

辅助性 T 细胞 17(Th17)细胞的特征是分泌白细胞介素 17(IL-17)细胞因子,对于抵抗细菌和真菌感染的免疫反应至关重要。尽管 Th17 细胞具有有益作用,但不受控制的 IL-17 产生可能导致免疫病理学和炎症性自身免疫性疾病,包括多发性硬化症、类风湿关节炎和炎症性肠病。尽管这些不同的结果是由 Th17 细胞的激活所驱动的,但 Th17 细胞的调节机制尚不完全清楚。发现 microRNAs(miRNAs)参与调节 Th17 细胞分化和功能,极大地提高了我们对 Th17 细胞在免疫反应和疾病中的理解。在这里,我们概述了 miRNA 的生物发生和功能,并总结了 miRNA 在 Th17 细胞分化和功能中的作用。最后,我们重点介绍了 miRNA 介导的 Th17 细胞命运失调在自身免疫性疾病中的最新进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65bf/8096907/ad13947bc438/fimmu-12-593473-g0001.jpg

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