首页> 外文OA文献 >Immune tolerance. Group 3 innate lymphoid cells mediate intestinal selection of commensal bacteria-specific CD4⁺ T cells
【2h】

Immune tolerance. Group 3 innate lymphoid cells mediate intestinal selection of commensal bacteria-specific CD4⁺ T cells

机译:免疫耐受。第3组先天性淋巴样细胞介导共生细菌特异性CD4 + T细胞的肠道选择

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Inflammatory CD4(+) T cell responses to self or commensal bacteria underlie the pathogenesis of autoimmunity and inflammatory bowel disease (IBD), respectively. Although selection of self-specific T cells in the thymus limits responses to mammalian tissue antigens, the mechanisms that control selection of commensal bacteria-specific T cells remain poorly understood. Here, we demonstrate that group 3 innate lymphoid cell (ILC3)-intrinsic expression of major histocompatibility complex class II (MHCII) is regulated similarly to thymic epithelial cells and that MHCII(+) ILC3s directly induce cell death of activated commensal bacteria-specific T cells. Further, MHCII on colonic ILC3s was reduced in pediatric IBD patients. Collectively, these results define a selection pathway for commensal bacteria-specific CD4(+) T cells in the intestine and suggest that this process is dysregulated in human IBD.
机译:自身或共生细菌的炎症性CD4(+)T细胞反应分别是自身免疫和炎症性肠病(IBD)的发病机理。尽管在胸腺中选择自我特异性T细胞限制了对哺乳动物组织抗原的反应,但控制共生细菌特异性T细胞选择的机制仍然知之甚少。在这里,我们证明了主要组织相容性复合体II类(MHCII)的第3组先天淋巴样细胞(ILC3)内在表达与胸腺上皮细胞相似,并且MHCII(+)ILC3s直接诱导活化的共生细菌特异性T细胞死亡细胞。此外,小儿IBD患者中结肠ILC3s上的MHCII减少。总的来说,这些结果定义了肠道中共生细菌特异性CD4(+)T细胞的选择途径,并表明该过程在人IBD中失调。

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号