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上皮内淋巴细胞通过 CD160/HVEM 信号促进肠道再生。

Intraepithelial lymphocytes promote intestinal regeneration through CD160/HVEM signaling.

机构信息

Institute for Immunology, Tsinghua University, Beijing, China; Department of Basic Medical Sciences, School of Medicine, Tsinghua University, Beijing, China; Beijing Key Lab for Immunological Research on Chronic Diseases, Tsinghua University, Beijing, China.

Institute for Immunology, Tsinghua University, Beijing, China.

出版信息

Mucosal Immunol. 2024 Apr;17(2):257-271. doi: 10.1016/j.mucimm.2024.02.004. Epub 2024 Feb 8.

DOI:10.1016/j.mucimm.2024.02.004
PMID:38340986
Abstract

Chemotherapy and radiotherapy frequently lead to intestinal damage. The mechanisms governing the repair or regeneration of intestinal damage are still not fully elucidated. Intraepithelial lymphocytes (IELs) are the primary immune cells residing in the intestinal epithelial layer. However, whether IELs are involved in intestinal epithelial injury repair remains unclear. Here, we found that IELs rapidly infiltrated the intestinal crypt region and are crucial for the recovery of the intestinal epithelium post-chemotherapy. Interestingly, IELs predominantly promoted intestinal regeneration by modulating the proliferation of transit-amplifying (TA) cells. Mechanistically, the expression of CD160 on IELs allows for interaction with herpes virus entry mediator (HVEM) on the intestinal epithelium, thereby activating downstream nuclear factor kappa (NF-κB) signaling and further promoting intestinal regeneration. Deficiency in either CD160 or HVEM resulted in reduced proliferation of intestinal progenitor cells, impaired intestinal damage repair, and increased mortality following chemotherapy. Remarkably, the adoptive transfer of CD160-sufficient IELs rescued the Rag1 deficient mice from chemotherapy-induced intestinal inflammation. Overall, our study underscores the critical role of IELs in intestinal regeneration and highlights the potential applications of targeting the CD160-HVEM axis for managing intestinal adverse events post-chemotherapy and radiotherapy.

摘要

化疗和放疗常导致肠道损伤。然而,肠道损伤修复的调控机制仍未完全阐明。上皮内淋巴细胞(IELs)是定居在肠道上皮层的主要免疫细胞。但是,IELs 是否参与肠道上皮损伤修复仍不清楚。在这里,我们发现 IELs 迅速浸润到肠隐窝区域,对于化疗后肠上皮的恢复至关重要。有趣的是,IELs 主要通过调节过渡扩增(TA)细胞的增殖来促进肠再生。从机制上讲,IELs 上 CD160 的表达允许与肠道上皮上的疱疹病毒进入介体(HVEM)相互作用,从而激活下游核因子 kappa(NF-κB)信号通路,并进一步促进肠再生。CD160 或 HVEM 的缺失导致肠祖细胞增殖减少、肠损伤修复受损以及化疗后死亡率增加。值得注意的是,CD160 充足的 IELs 的过继转移可使 Rag1 缺陷小鼠免受化疗引起的肠道炎症。总的来说,我们的研究强调了 IELs 在肠再生中的关键作用,并突出了靶向 CD160-HVEM 轴以管理化疗和放疗后肠道不良事件的潜在应用。

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Intraepithelial lymphocytes promote intestinal regeneration through CD160/HVEM signaling.上皮内淋巴细胞通过 CD160/HVEM 信号促进肠道再生。
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