先天性淋巴细胞
生物
免疫学
先天免疫系统
微生物群
平衡
炎症性肠病
肠道菌群
免疫系统
人口
炎症
获得性免疫系统
免疫
细胞生物学
CTLA-4号机组
疾病
T细胞
医学
遗传学
病理
环境卫生
作者
Jonathan W. Lo,Jan-Hendrik Schroeder,Luke B. Roberts,Rami Mohamed,Domenico Cozzetto,Gordon Beattie,Omer Omer,Ellen M. Ross,Frank Heuts,Geraldine M. Jowett,Emily Read,Matthew Madgwick,Joana F. Neves,Tamás Korcsmáros,Richard G. Jenner,Lucy S. K. Walker,Nick Powell,Graham M. Lord
标识
DOI:10.1038/s41467-024-51719-6
摘要
The maintenance of intestinal homeostasis is a fundamental process critical for organismal integrity. Sitting at the interface of the gut microbiome and mucosal immunity, adaptive and innate lymphoid populations regulate the balance between commensal micro-organisms and pathogens. Checkpoint inhibitors, particularly those targeting the CTLA-4 pathway, disrupt this fine balance and can lead to inflammatory bowel disease and immune checkpoint colitis. Here, we show that CTLA-4 is expressed by innate lymphoid cells and that its expression is regulated by ILC subset-specific cytokine cues in a microbiota-dependent manner. Genetic deletion or antibody blockade of CTLA-4 in multiple in vivo models of colitis demonstrates that this pathway plays a key role in intestinal homeostasis. Lastly, we have found that this observation is conserved in human IBD. We propose that this population of CTLA-4-positive ILC may serve as an important target for the treatment of idiopathic and iatrogenic intestinal inflammation.
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