| Literature DB >> 31497905 |
Pei Yang1, Fei-Ya Qian1, Ming-Fei Zhang1, A-Lan Xu1, Xiang Wang1, Bao-Ping Jiang1, Ling-Ling Zhou1.
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. ©2019 Society for Leukocyte Biology.Entities:
Keywords: Th17 cells; pathogenicity; plasticity; rheumatoid arthritis
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Year: 2019 PMID: 31497905 DOI: 10.1002/JLB.4RU0619-197R
Source DB: PubMed Journal: J Leukoc Biol ISSN: 0741-5400 Impact factor: 4.962