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肠道免疫耐受和组织稳态的早期生活印迹。

Early life imprinting of intestinal immune tolerance and tissue homeostasis.

机构信息

Immunology and Microbial Pathogenesis Program, Weill Cornell Medicine Graduate School of Medical Sciences, New York, New York, USA.

Immuno-Oncology, Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, New York, USA.

出版信息

Immunol Rev. 2024 May;323(1):303-315. doi: 10.1111/imr.13321. Epub 2024 Mar 19.

Abstract

Besides its canonical role in protecting the host from pathogens, the immune system plays an arguably equally important role in maintaining tissue homeostasis. Within barrier tissues that interface with the external microenvironment, induction of immune tolerance to innocuous antigens, such as commensal, dietary, and environmental antigens, is key to establishing immune homeostasis. The early postnatal period represents a critical window of opportunity in which parallel development of the tissue, immune cells, and microbiota allows for reciprocal regulation that shapes the long-term immunological tone of the tissue and subsequent risk of immune-mediated diseases. During early infancy, the immune system appears to sacrifice pro-inflammatory functions, prioritizing the establishment of tissue tolerance. In this review, we discuss mechanisms underlying early life windows for intestinal tolerance with a focus on newly identified RORγt antigen-presenting cells-Thetis cells-and highlight the role of the intestinal microenvironment in shaping intestinal immune system development and tolerance.

摘要

除了其在保护宿主免受病原体侵害方面的规范作用外,免疫系统在维持组织内稳态方面也起着同样重要的作用。在与外部微环境交界的屏障组织中,诱导对无害抗原(如共生、饮食和环境抗原)的免疫耐受对于建立免疫内稳态至关重要。出生后的早期阶段是一个关键的机会窗口,在此期间,组织、免疫细胞和微生物群的平行发育允许相互调节,从而塑造组织的长期免疫基调以及随后免疫介导疾病的风险。在婴儿早期,免疫系统似乎牺牲了促炎功能,优先建立组织耐受。在这篇综述中,我们讨论了肠道耐受的早期生命窗口的机制,重点介绍了新发现的 RORγt 抗原呈递细胞——忒提斯细胞,并强调了肠道微环境在塑造肠道免疫系统发育和耐受中的作用。

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