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肠道微生物特异性 T 细胞的胸腺发育。

Thymic development of gut-microbiota-specific T cells.

机构信息

Immunology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

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

出版信息

Nature. 2021 Jun;594(7863):413-417. doi: 10.1038/s41586-021-03531-1. Epub 2021 May 12.


DOI:10.1038/s41586-021-03531-1
PMID:33981034
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8323488/
Abstract

Humans and their microbiota have coevolved a mutually beneficial relationship in which the human host provides a hospitable environment for the microorganisms and the microbiota provides many advantages for the host, including nutritional benefits and protection from pathogen infection. Maintaining this relationship requires a careful immune balance to contain commensal microorganisms within the lumen while limiting inflammatory anti-commensal responses. Antigen-specific recognition of intestinal microorganisms by T cells has previously been described. Although the local environment shapes the differentiation of effector cells it is unclear how microbiota-specific T cells are educated in the thymus. Here we show that intestinal colonization in early life leads to the trafficking of microbial antigens from the intestine to the thymus by intestinal dendritic cells, which then induce the expansion of microbiota-specific T cells. Once in the periphery, microbiota-specific T cells have pathogenic potential or can protect against related pathogens. In this way, the developing microbiota shapes and expands the thymic and peripheral T cell repertoire, allowing for enhanced recognition of intestinal microorganisms and pathogens.

摘要

人类及其微生物群共同进化出一种互利共生的关系,在这种关系中,人类宿主为微生物提供了一个适宜的环境,而微生物群则为主机提供了许多优势,包括营养益处和防止病原体感染。维持这种关系需要一种精细的免疫平衡,以将腔道内的共生微生物限制在其中,同时限制针对共生微生物的炎症反应。T 细胞对肠道微生物的抗原特异性识别以前已有描述。尽管局部环境塑造了效应细胞的分化,但尚不清楚肠道特异性 T 细胞在胸腺中是如何被教育的。在这里,我们表明,早期生命中的肠道定植导致肠道树突状细胞将微生物抗原从肠道运送到胸腺,从而诱导肠道特异性 T 细胞的扩增。一旦进入外周,肠道特异性 T 细胞就具有潜在的致病性,或者可以预防相关病原体。通过这种方式,不断发展的微生物群塑造和扩展了胸腺和外周 T 细胞库,增强了对肠道微生物和病原体的识别。

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本文引用的文献

[1]
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Immunity. 2020-12-15

[2]
Toxin-Triggered Interleukin-1 Receptor Signaling Enables Early-Life Discrimination of Pathogenic versus Commensal Skin Bacteria.

Cell Host Microbe. 2019-11-26

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Curr Protoc Immunol. 2019-6

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Nat Immunol. 2019-1-14

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Cell Host Microbe. 2018-12-20

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Immunity. 2018-7-3

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c-MAF-dependent regulatory T cells mediate immunological tolerance to a gut pathobiont.

Nature. 2018-2-7

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IgA-coated enriched in Crohn's disease spondyloarthritis promote T17-dependent inflammation.

Sci Transl Med. 2017-2-8

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A Wave of Regulatory T Cells into Neonatal Skin Mediates Tolerance to Commensal Microbes.

Immunity. 2015-11-17

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An IL-23R/IL-22 Circuit Regulates Epithelial Serum Amyloid A to Promote Local Effector Th17 Responses.

Cell. 2015-10-8

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