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树突状细胞在静息状态下激活 T 细胞的多样化结果。

Variegated Outcomes of T Cell Activation by Dendritic Cells in the Steady State.

机构信息

Department of Molecular Microbiology and Immunology, Saint Louis University School of Medicine, St. Louis, MO.

Department of Molecular Microbiology and Immunology, Saint Louis University School of Medicine, St. Louis, MO

出版信息

J Immunol. 2022 Feb 1;208(3):539-547. doi: 10.4049/jimmunol.2100932.


DOI:10.4049/jimmunol.2100932
PMID:35042789
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8852351/
Abstract

Conventional dendritic cells (cDC) control adaptive immunity by sensing damage- and pathogen-associated molecular patterns and then inducing defined differentiation programs in T cells. Nevertheless, in the absence of specific proimmunogenic innate signals, generally referred to as the steady state, cDC also activate T cells to induce specific functional fates. Consistent with the maintenance of homeostasis, such specific outcomes of T cell activation in the steady state include T cell clonal anergy, deletion, and conversion of peripheral regulatory T cells (pTregs). However, the robust induction of protolerogenic mechanisms must be reconciled with the initiation of autoimmune responses and cancer immunosurveillance that are also observed under homeostatic conditions. Here we review the diversity of fates and functions of T cells involved in the opposing immunogenic and tolerogenic processes induced in the steady state by the relevant mechanisms of systemic cDC present in murine peripheral lymphoid organs.

摘要

传统树突状细胞 (cDC) 通过感知损伤相关和病原体相关的分子模式来控制适应性免疫,然后诱导 T 细胞的特定分化程序。然而,在没有特定的促免疫原性先天信号(通常称为稳态)的情况下,cDC 也会激活 T 细胞以诱导特定的功能命运。与维持体内平衡一致,稳态中 T 细胞激活的这种特定结果包括 T 细胞克隆无反应性、缺失和外周调节性 T 细胞 (pTreg) 的转化。然而,必须协调强烈诱导的耐受原性机制与在稳态下观察到的自身免疫反应和癌症免疫监视的启动。在这里,我们回顾了参与由存在于鼠外周淋巴器官中的系统性 cDC 的相关机制在稳态下诱导的免疫原性和耐受原性过程的 T 细胞的各种命运和功能。

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Variegated Outcomes of T Cell Activation by Dendritic Cells in the Steady State.

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[5]
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[6]
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[7]
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本文引用的文献

[1]
Lung dendritic cells migrate to the spleen to prime long-lived TCF1 memory CD8 T cell precursors after influenza infection.

Sci Immunol. 2021-9-10

[2]
Current and Future Immunotherapies for Multiple Sclerosis.

Mo Med. 2021

[3]
Type 1 conventional dendritic cells and interferons are required for spontaneous CD4 and CD8 T-cell protective responses to breast cancer.

Clin Transl Immunology. 2021-7-14

[4]
The formation of pre-effectors in the steady state opens a new perspective for cancer immunosurveillance.

Oncotarget. 2021-6-22

[5]
A local regulatory T cell feedback circuit maintains immune homeostasis by pruning self-activated T cells.

Cell. 2021-7-22

[6]
Induction of antigen-specific tolerance by nanobody-antigen adducts that target class-II major histocompatibility complexes.

Nat Biomed Eng. 2021-11

[7]
Dendritic Cell Regulation of T Helper Cells.

Annu Rev Immunol. 2021-4-26

[8]
Gut Helicobacter presentation by multiple dendritic cell subsets enables context-specific regulatory T cell generation.

Elife. 2021-2-3

[9]
Dendritic Cells Revisited.

Annu Rev Immunol. 2021-4-26

[10]
The receptor DNGR-1 signals for phagosomal rupture to promote cross-presentation of dead-cell-associated antigens.

Nat Immunol. 2021-2

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