Transcriptional Regulators of T Helper 17 Cell Differentiation in Health and Autoimmune Diseases

被引:124
|
作者
Capone, Alessia [1 ,2 ]
Volpe, Elisabetta [1 ]
机构
[1] IRCSS Fdn Santa Lucia, Neuroimmunol Unit, Rome, Italy
[2] Sapienza Univ, Dept Biol & Biotechnol Charles Darwin, Rome, Italy
来源
FRONTIERS IN IMMUNOLOGY | 2020年 / 11卷
关键词
T helper 17 cells; interleukin-17; retinoic acid receptor related orphan nuclear receptor gamma t; multiple sclerosis; Crohn's disease; rheumatoid arthritis; psoriasis; ROR-GAMMA-T; KAPPA-B-ZETA; ORPHAN NUCLEAR RECEPTORS; INDUCIBLE FACTOR HIF; RUNX1; BINDING-SITE; GROWTH-FACTOR-BETA; TH17; CELLS; T(H)17 DIFFERENTIATION; INDUCED ARTHRITIS; IL-17;
D O I
10.3389/fimmu.2020.00348
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T helper (Th) 17 cells are a subtype of CD4 T lymphocytes characterized by the expression of retinoic acid-receptor (RAR)-related orphan receptor (ROR)gamma t transcription factor, encoded by gene Rorc. These cells are implicated in the pathology of autoimmune inflammatory disorders as well as in the clearance of extracellular infections. The main function of Th17 cells is the production of cytokine called interleukin (IL)-17A. This review highlights recent advances in mechanisms regulating transcription of IL-17A. In particular, we described the lineage defining transcription factor ROR gamma t and other factors that regulate transcription of Il17a or Rorc by interacting with ROR gamma t or by binding their specific DNA regions, which may positively or negatively influence their expression. Moreover, we reported the eventual involvement of those factors in Th17-related diseases, such as multiple sclerosis, rheumatoid arthritis, psoriasis, and Crohn's disease, characterized by an exaggerated Th17 response. Finally, we discussed the potential new therapeutic approaches for Th17-related diseases targeting these transcription factors. The wide knowledge of transcriptional regulators of Th17 cells is crucial for the better understanding of the pathogenic role of these cells and for development of therapeutic strategies aimed at fighting Th17-related diseases.
引用
收藏
页数:8
相关论文
共 50 条
  • [41] Revisiting the old link between infection and autoimmune disease with commensals and T helper 17 cells
    Blander, J. Magarian
    Torchinsky, Miriam B.
    Campisi, Laura
    IMMUNOLOGIC RESEARCH, 2012, 54 (1-3) : 50 - 68
  • [42] The T helper 17-regulatory T cell axis in transplant rejection and tolerance
    Mitchell, Peter
    Afzali, Behdad
    Lombardi, Giovanna
    Lechler, Robert I.
    CURRENT OPINION IN ORGAN TRANSPLANTATION, 2009, 14 (04) : 326 - 331
  • [43] Defining the human T helper 17 cell phenotype
    Annunziato, Francesco
    Cosmi, Lorenzo
    Liotta, Francesco
    Maggi, Enrico
    Romagnani, Sergio
    TRENDS IN IMMUNOLOGY, 2012, 33 (10) : 505 - 512
  • [44] Epigenetic activation during T helper 17 cell differentiation is mediated by Tripartite motif containing 28
    Jiang, Yu
    Liu, Ying
    Lu, Huiping
    Sun, Shao-Cong
    Jin, Wei
    Wang, Xiaohu
    Dong, Chen
    NATURE COMMUNICATIONS, 2018, 9
  • [46] From interleukin-23 to T-helper 17 cells: human T-helper cell differentiation revisited
    Boniface, Katia
    Blom, Bianca
    Liu, Yong-Jun
    Malefyt, Rene de Waal
    IMMUNOLOGICAL REVIEWS, 2008, 226 : 132 - 146
  • [47] Targeting T-cell integrins in autoimmune and inflammatory diseases
    Kelly, Aidan J.
    Long, Aideen
    CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2023, : 15 - 26
  • [48] The T helper type 17/regulatory T cell paradigm in pregnancy
    Figueiredo, Ana Sofia
    Schumacher, Anne
    IMMUNOLOGY, 2016, 148 (01) : 13 - 21
  • [49] Molecular mechanisms of T helper 17 cell differentiation: Emerging roles for transcription cofactors
    Jiang, Yu
    Wang, Xiaohu
    Dong, Chen
    ADVANCES IN IMMUNOLOGY IN CHINA, PT A, 2019, 144 : 121 - 153
  • [50] Dysregulated MicroRNA involvement in Multiple Sclerosis by induction of T Helper 17 Cell Differentiation
    Chen, Chen
    Zhou, Yifan
    Wang, Jingqi
    Yan, Yaping
    Peng, Lisheng
    Qiu, Wei
    FRONTIERS IN IMMUNOLOGY, 2018, 9