控制TH17细胞发生在小肠中
Enric Esplugues1, Samuel Huber, Nicola Gagliani
1Department of Immunobiology, Yale University School of Medicine, New Haven, Connecticut 06520, USA. enric.esplugues@yale.edu
Nature
|July 19, 2011
概括
亲炎性T辅助17 (T(H) 17细胞,涉及到自身免疫性疾病,在小肠中受到控制. 它们被消除或转化为调节性T(H) 17细胞,限制它们的致病性.
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:
- 产生中白素-17的T辅助细胞 (T(H) 17) 是一个独特的CD4(+) T细胞子集.
- T(H) 17细胞是自身免疫性疾病的关键驱动因素,如实验性自身免疫性脑膜炎 (EAE).
- 在体内控制T(H) 17细胞的机制在很大程度上是未知的.
研究的目的:
- 研究免疫系统如何以及在哪里控制亲炎性T17细胞 in vivo.
- 确定负责限制T(H) 17细胞致病性的机制.
主要方法:
- 使用了耐受性诱导,败血症和流感A型病毒感染 (H1N1) 的模型.
- 研究了通过CCR6/CCL20轴的T(H) 17细胞迁移.
- 在小肠中评估了T(H) 17细胞清除和表型转化.
主要成果:
- 支持炎症的T(H) 17细胞迁移到小肠,并在小肠内受到控制.
- 在小肠中CCL20化学激素的表达促进了T(H) 17细胞的同源化.
- 细胞通过肠膜排出或获得调节性,免疫抑制性质 (rT(H) 17).
结论:
- 小肠是控制致病性T(H) 17细胞的关键位置.
- 机制包括消除和转化为调节性T(H) 17细胞,减轻自身免疫反应.
- 这些发现突显了胃肠道在免疫平衡和T(H) 17细胞调节中的作用.
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