Horn Veronika, Sonnenberg Gregory F
Jill Roberts Institute for Research in Inflammatory Bowel Disease, Weill Cornell Medicine, Cornell University, New York, NY, USA.
Joan and Sanford I. Weill Department of Medicine, Division of Gastroenterology & Hepatology, Weill Cornell Medicine, Cornell University, New York, NY, USA.
Nat Rev Gastroenterol Hepatol. 2024 Jun;21(6):428-443. doi: 10.1038/s41575-024-00906-3. Epub 2024 Mar 11.
The gastrointestinal tract is an immunologically rich organ, containing complex cell networks and dense lymphoid structures that safeguard this large absorptive barrier from pathogens, contribute to tissue physiology and support mucosal healing. Simultaneously, the immune system must remain tolerant to innocuous dietary antigens and trillions of normally beneficial microorganisms colonizing the intestine. Indeed, a dysfunctional immune response in the intestine underlies the pathogenesis of numerous local and systemic diseases, including inflammatory bowel disease, food allergy, chronic enteric infections or cancers. Here, we discuss group 3 innate lymphoid cells (ILC3s), which have emerged as orchestrators of tissue physiology, immunity, inflammation, tolerance and malignancy in the gastrointestinal tract. ILC3s are abundant in the developing and healthy intestine but their numbers or function are altered during chronic disease and cancer. The latest studies provide new insights into the mechanisms by which ILC3s fundamentally shape intestinal homeostasis or disease pathophysiology, and often this functional dichotomy depends on context and complex interactions with other cell types or microorganisms. Finally, we consider how this knowledge could be harnessed to improve current treatments or provoke new opportunities for therapeutic intervention to promote gut health.
胃肠道是一个免疫丰富的器官,包含复杂的细胞网络和密集的淋巴结构,这些结构保护这个巨大的吸收屏障免受病原体侵害,有助于组织生理功能并支持黏膜愈合。同时,免疫系统必须对无害的饮食抗原和数以万亿计正常定殖于肠道的有益微生物保持耐受。事实上,肠道免疫反应功能失调是众多局部和全身性疾病发病机制的基础,包括炎症性肠病、食物过敏、慢性肠道感染或癌症。在此,我们讨论3型固有淋巴细胞(ILC3s),它们已成为胃肠道组织生理、免疫、炎症、耐受和恶性肿瘤的协调者。ILC3s在发育中的和健康的肠道中大量存在,但在慢性疾病和癌症期间其数量或功能会发生改变。最新研究为ILC3s从根本上塑造肠道稳态或疾病病理生理学的机制提供了新见解,而且这种功能二分法通常取决于背景以及与其他细胞类型或微生物的复杂相互作用。最后,我们思考如何利用这些知识来改进当前的治疗方法或为促进肠道健康的治疗干预带来新机遇。