Sun-Yat Sen University, School of Medicine, Guangzhou, China.
Experimental Immunology Branch, National Cancer Institute, National Institute of Health (NIH), Bethesda, MD, United States.
Front Immunol. 2022 Jul 4;13:951339. doi: 10.3389/fimmu.2022.951339. eCollection 2022.
It has been well established that Foxp3+ regulatory T cells (Treg cells) play a crucial role for immune repression and tolerance, protecting the body from autoimmunity and inflammation. Previous studies indicate that intestinal Treg cells are one specialized population of Treg cells, distinct from those in other organ compartments, both functionally and phenotypically. Specific external and internal signals, particularly the presence of microbiota, shape these Treg cells to better cooperate with the gut ecosystem, controlling intestinal physiology. The integrity of intestinal epithelial barrier represents a key feature of gut immune tolerance, which can be regulated by multiple factors. Emerging evidence suggests that bidirectional interactions between gut epithelium and resident T cells significantly contribute to intestinal barrier function. Understanding how Treg cells regulate intestinal barrier integrity provides insights into immune tolerance-mediated mucosal homeostasis, which can further illuminate potential therapeutic strategies for treating inflammatory bowel disease and colon cancer.
已经证实,Foxp3+ 调节性 T 细胞(Treg 细胞)在免疫抑制和耐受中发挥着关键作用,保护身体免受自身免疫和炎症的侵害。先前的研究表明,肠道 Treg 细胞是 Treg 细胞的一个特殊群体,在功能和表型上都与其他器官隔室中的 Treg 细胞不同。特定的外部和内部信号,特别是微生物群的存在,使这些 Treg 细胞更好地与肠道生态系统合作,控制肠道生理。肠道上皮屏障的完整性是肠道免疫耐受的一个关键特征,它可以受到多种因素的调节。新出现的证据表明,肠道上皮和固有 T 细胞之间的双向相互作用对肠道屏障功能有重要贡献。了解 Treg 细胞如何调节肠道屏障的完整性,有助于我们理解免疫耐受介导的黏膜稳态,这也为治疗炎症性肠病和结肠癌的潜在治疗策略提供了启示。