在发炎性T细胞的产生过程中,IL-21对自身蛋白调节至关重要
Roza Nurieva1, Xuexian O Yang, Gustavo Martinez
1Department of Immunology, M. D. Anderson Cancer Center, Houston, Texas 77030, USA. rnurieva@mdanderson.org
Nature
|June 22, 2007
概括
干白素-21 (IL-21) 对于T辅助细胞17 (T(H) 17的分化至关重要,作为一种自因子. 它的缺乏可以保护自身免疫性疾病,突出显示IL-21作为治疗点.
科学领域:
- 免疫学 免疫学 免疫学
- 细胞生物学 细胞生物学
背景情况:
- CD4+辅助T细胞分化成T(H) 1和T(H) 2等子集,每个子集都有独特的功能.
- 一个独特的子集T(H) 17细胞,介导组织炎症,并由特定的细胞因子和转录因子诱导.
研究的目的:
- 调查介素-21 (IL-21) 在T(H) 17细胞分化中的作用及其作为炎症疾病治疗点的潜力.
主要方法:
- 在小鼠T(H) 17细胞中分析细胞因子表达.
- 研究IL-6对IL-21的诱导及其对STAT3和ROR-gamma的依赖.
- 评估IL-21对T(H) 17分化和Foxp3表达的影响.
- 评估IL-21缺乏对实验性自身免疫脑膜炎的影响.
主要成果:
- IL-21在小鼠T(H) 17细胞中高度表达,并以STAT3依赖的方式由IL-6诱导.
- IL-21强烈诱导T(H) 17分化并抑制Foxp3表达,需要STAT3和ROR-gamma.
- 缺少IL-21会损害T(H) 17细胞的产生,并提供对实验性自身免疫脑膜炎的保护.
结论:
- IL-21作为一个足够的和必要的自克林细胞因子,用于T (H) 17的分化.
- IL-21代表了管理炎症性疾病的潜在治疗标.
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