免疫学
白细胞介素17
发病机制
RAR相关孤儿受体γ
CTLA-4号机组
白细胞介素23
炎症性肠病
白细胞介素12
多发性硬化
自身免疫
白细胞介素21
生物
炎症
医学
T细胞
细胞毒性T细胞
免疫系统
疾病
FOXP3型
体外
遗传学
病理
作者
Alí N. Kamali,Seyedeh Masoomeh Noorbakhsh,Haleh Hamedifar,Farhad Jadidi‐Niaragh,Reza Yazdani,José M. Bautista,Gholamreza Azizi
标识
DOI:10.1016/j.molimm.2018.11.015
摘要
The T helper 17 (Th17) cells contain a dynamic subset of CD4+ T-cells that are able to develop into other different lineage subsets, including the Th1-like Th17 cells. These cells co-express retinoic acid-related orphan receptor gamma t (RORγt) and transcription factor T-box-expressed-in-T-cells (T-bet) and produce both interleukin (IL)-17 and interferon (IFN)-γ. Recent reports have shown that Th1-like Th17 cells play crucial roles in the pathogenesis of autoimmune diseases such as inflammatory bowel disease, multiple sclerosis and rheumatoid arthritis, as well as, some primary immunodeficiency with autoimmune features. Here, the actual mechanisms for Th17 cells plasticity to Th1-like Th17 cells are discussed and reviewed in association to the role that Th1-like Th17 cells have on inflammatory and autoimmune disorders.
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