Hou Qihang, Huang Jingxi, Ayansola Hammed, Masatoshi Hori, Zhang Bingkun
State Key Laboratory of Animal Nutrition, Department of Animal Nutrition & Feed Science, College of Animal Science & Technology, China Agricultural University, Haidian District, Beijing, China.
Department of Veterinary Pharmacology, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Bunkyo-ku, Tokyo, Japan.
Front Immunol. 2021 Jan 20;11:623691. doi: 10.3389/fimmu.2020.623691. eCollection 2020.
The mammalian intestine is the largest immune organ that contains the intestinal stem cells (ISC), differentiated epithelial cells (enterocytes, Paneth cells, goblet cells, tuft cells, etc.), and gut resident-immune cells (T cells, B cells, dendritic cells, innate lymphoid cell, etc.). Inflammatory bowel disease (IBD), a chronic inflammatory disease characterized by mucosa damage and inflammation, threatens the integrity of the intestine. The continuous renewal and repair of intestinal mucosal epithelium after injury depend on ISCs. Inflamed mucosa healing could be a new target for the improvement of clinical symptoms, disease recurrence, and resection-free survival in IBD treated patients. The knowledge about the connections between ISC and immune cells is expanding with the development of intestinal organoid culture and single-cell RNA sequencing technology. Recent findings implicate that immune cells such as T cells, ILCs, dendritic cells, and macrophages and cytokines secreted by these cells are critical in the regeneration of ISCs and intestinal epithelium. Transplantation of ISC to the inflamed mucosa may be a new therapeutic approach to reconstruct the epithelial barrier in IBD. Considering the links between ISC and immune cells, we predict that the integration of biological agents and ISC transplantation will revolutionize the future therapy of IBD patients.
哺乳动物的肠道是最大的免疫器官,包含肠道干细胞(ISC)、分化的上皮细胞(肠上皮细胞、潘氏细胞、杯状细胞、簇状细胞等)和肠道常驻免疫细胞(T细胞、B细胞、树突状细胞、固有淋巴细胞等)。炎症性肠病(IBD)是一种以黏膜损伤和炎症为特征的慢性炎症性疾病,威胁着肠道的完整性。损伤后肠道黏膜上皮的持续更新和修复依赖于ISC。炎症黏膜愈合可能是改善IBD患者临床症状、疾病复发和无切除生存率的新靶点。随着肠道类器官培养和单细胞RNA测序技术的发展,关于ISC与免疫细胞之间联系的知识正在不断扩展。最近的研究结果表明,T细胞、固有淋巴细胞、树突状细胞和巨噬细胞等免疫细胞以及这些细胞分泌的细胞因子在ISC和肠上皮的再生中至关重要。将ISC移植到炎症黏膜可能是重建IBD上皮屏障的一种新的治疗方法。考虑到ISC与免疫细胞之间的联系,我们预测生物制剂与ISC移植的结合将彻底改变IBD患者的未来治疗。