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维甲酸相关孤儿受体γt 上皮内抗原呈递细胞介导口服耐受和调节性T细胞诱导。

RORγt eTACs mediate oral tolerance and Treg induction.

作者信息

Sun Im-Hong, Qualls Anita E, Yin Han S, Wang Jiaxi, Arvedson Matthew P, Germino Joe, Horner Nolan K, Zhong Sheng, Du Juan, Valdearcos Martin, Ntranos Vasilis, Locksley Richard M, Ricardo-Gonzalez Roberto R, Gardner James M

机构信息

Department of Surgery, University of California, San Francisco, San Francisco, CA, USA.

Diabetes Center, University of California, San Francisco , San Francisco, CA, USA.

出版信息

J Exp Med. 2025 Aug 4;222(8). doi: 10.1084/jem.20250573. Epub 2025 Apr 29.


DOI:10.1084/jem.20250573
PMID:40298935
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12039581/
Abstract

The immune system must distinguish pathogens from innocuous dietary antigens, but the precise mechanisms and cellular actors remain unclear. Here, we demonstrate that RORγt-lineage APCs are required for oral tolerance. Using lineage tracing and single-cell sequencing, we show these APCs consist of three principal populations: type 3 innate lymphoid cells (ILC3s), RORγt-lineage dendritic cells, and cells expressing Aire called RORγt eTACs (R-eTACs)-also known as Janus or Thetis cells. We show that R-eTACs, but not ILC3s, are required for oral tolerance induction. We find R-eTACs are of probable myeloid origin and uniquely express integrin β8 (Itgb8). Both MHCII and Itgb8 expression in RORγt-lineage cells are necessary to induce food-specific regulatory T cells. Mice lacking R-eTACs or with deletion of MHCII or Itgb8 in the RORγt lineage fail to generate Tregs and instead develop a T-follicular helper response with elevated antigen-specific antibodies. These findings establish R-eTACs as critical mediators of oral tolerance and suggest novel cellular targets to modulate immune tolerance.

摘要

免疫系统必须区分病原体与无害的饮食抗原,但其确切机制和细胞作用因子仍不清楚。在此,我们证明RORγt谱系的抗原呈递细胞(APC)是口服耐受所必需的。通过谱系追踪和单细胞测序,我们发现这些APC由三个主要群体组成:3型天然淋巴细胞(ILC3)、RORγt谱系树突状细胞以及表达Aire的细胞,称为RORγt eTAC(R-eTAC),也称为Janus细胞或Thetis细胞。我们表明,口服耐受诱导需要R-eTAC,而不是ILC3。我们发现R-eTAC可能起源于髓系,且独特地表达整合素β8(Itgb8)。RORγt谱系细胞中MHCII和Itgb8的表达对于诱导食物特异性调节性T细胞都是必需的。缺乏R-eTAC或RORγt谱系中MHCII或Itgb8缺失的小鼠无法产生调节性T细胞,反而会产生抗原特异性抗体水平升高的T滤泡辅助细胞反应。这些发现确立了R-eTAC作为口服耐受的关键介质,并提示了调节免疫耐受的新细胞靶点。

相似文献

[1]
RORγt eTACs mediate oral tolerance and Treg induction.

J Exp Med. 2025-8-4

[2]
PRDM16-dependent antigen-presenting cells induce tolerance to gut antigens.

Nature. 2025-4-14

[3]
"What's in a name?" Clarifying the identity of RORγt+ antigen-presenting cells.

J Exp Med. 2025-8-4

[4]
β8 Integrin Expression and Activation of TGF-β by Intestinal Dendritic Cells Are Determined by Both Tissue Microenvironment and Cell Lineage.

J Immunol. 2016-9-1

[5]
Rorγt-positive dendritic cells are required for the induction of peripheral regulatory T cells in response to oral antigens.

Cell. 2025-5-15

[6]
RORγt-expressing dendritic cells are functionally versatile and evolutionarily conserved antigen-presenting cells.

Proc Natl Acad Sci U S A. 2025-3-4

[7]
Functional targeting of ILC2s and ILC3s reveals selective roles in intestinal fibrosis and homeostasis.

J Exp Med. 2025-7-7

[8]
Novel antigen-presenting cell imparts T-dependent tolerance to gut microbiota.

Nature. 2022-10

[9]
A distinct human cell type expressing MHCII and RORγt with dual characteristics of dendritic cells and type 3 innate lymphoid cells.

Proc Natl Acad Sci U S A. 2023-12-26

[10]
Eosinophils Contribute to Oral Tolerance via Induction of RORγt-Positive Antigen-Presenting Cells and RORγt-Positive Regulatory T Cells.

Biomolecules. 2024-1-10

引用本文的文献

[1]
RORγt antigen-presenting cells mediate food tolerance.

Nat Rev Immunol. 2025-5-29

[2]
Thetis cells: regulators of intestinal immune tolerance.

Curr Opin Immunol. 2025-8

本文引用的文献

[1]
PRDM16-dependent antigen-presenting cells induce tolerance to gut antigens.

Nature. 2025-4-14

[2]
RORγt-expressing dendritic cells are functionally versatile and evolutionarily conserved antigen-presenting cells.

Proc Natl Acad Sci U S A. 2025-3-4

[3]
Identification of antigen-presenting cell-T cell interactions driving immune responses to food.

Science. 2025-3-14

[4]
The right educational environment: Oral tolerance in early life.

Immunol Rev. 2024-9

[5]
Early life imprinting of intestinal immune tolerance and tissue homeostasis.

Immunol Rev. 2024-5

[6]
Automatic cell-type harmonization and integration across Human Cell Atlas datasets.

Cell. 2023-12-21

[7]
A distinct human cell type expressing MHCII and RORγt with dual characteristics of dendritic cells and type 3 innate lymphoid cells.

Proc Natl Acad Sci U S A. 2023-12-26

[8]
The emerging family of RORγt antigen-presenting cells.

Nat Rev Immunol. 2024-1

[9]
ICOS costimulation is indispensable for the differentiation of T follicular regulatory cells.

Life Sci Alliance. 2023-4

[10]
ILC3s select microbiota-specific regulatory T cells to establish tolerance in the gut.

Nature. 2022-10

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