Wu Zhengyu, Chen Xingchi, Han Fei, Leeansyah Edwin
Institute of Biopharmaceutical and Health Engineering, Tsinghua Shenzhen International Graduate School, Tsinghua University, Shenzhen 518055, China.
Sci Adv. 2025 Feb 7;11(6):eadu4172. doi: 10.1126/sciadv.adu4172.
Mucosa-associated invariant T (MAIT) cells are a large population of unconventional T cells widely distributed in the human gastrointestinal tract. Their homing to the gut is central to maintaining mucosal homeostasis and immunity. This review discusses the potential mechanisms that guide MAIT cells to the intestinal mucosa during homeostasis and inflammation, emphasizing the roles of chemokines, chemokine receptors, and tissue adhesion molecules. The potential influence of the gut microbiota on MAIT cell homing to different regions of the human gut is also discussed. Last, we introduce how organoid technology offers a potentially valuable approach to advance our understanding of MAIT cell tissue homing by providing a more physiologically relevant model that mimics the human gut tissue. These models may enable a detailed investigation of the gut-specific homing mechanisms of MAIT cells. By understanding the regulation of MAIT cell homing to the human gut, potential avenues for therapeutic interventions targeting gut inflammatory conditions such as inflammatory bowel diseases (IBD) may emerge.
黏膜相关恒定T(MAIT)细胞是一大群广泛分布于人类胃肠道的非常规T细胞。它们归巢至肠道对于维持黏膜稳态和免疫至关重要。本综述讨论了在稳态和炎症期间引导MAIT细胞至肠道黏膜的潜在机制,重点强调趋化因子、趋化因子受体和组织黏附分子的作用。还讨论了肠道微生物群对MAIT细胞归巢至人类肠道不同区域的潜在影响。最后,我们介绍类器官技术如何通过提供一个更能模拟人类肠道组织的生理相关模型,为推进我们对MAIT细胞组织归巢的理解提供一种潜在有价值的方法。这些模型可能有助于详细研究MAIT细胞的肠道特异性归巢机制。通过了解MAIT细胞归巢至人类肠道的调控机制,可能会出现针对肠道炎症性疾病(IBD)等肠道炎性病症的治疗干预潜在途径。