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免疫网络中成纤维细胞与 T 细胞的串扰。

Crosstalk between fibroblasts and T cells in immune networks.

机构信息

Department of Dermatology, College of Medicine, Pusan National University, Busan, Republic of Korea.

Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology, Daejeon, Republic of Korea.

出版信息

Front Immunol. 2023 Jan 9;13:1103823. doi: 10.3389/fimmu.2022.1103823. eCollection 2022.


DOI:10.3389/fimmu.2022.1103823
PMID:36700220
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9868862/
Abstract

Fibroblasts are primarily considered as cells that support organ structures and are currently receiving attention for their roles in regulating immune responses in health and disease. Fibroblasts are assigned distinct phenotypes and functions in different organs owing to their diverse origins and functions. Their roles in the immune system are multifaceted, ranging from supporting homeostasis to inducing or suppressing inflammatory responses of immune cells. As a major component of immune cells, T cells are responsible for adaptive immune responses and are involved in the exacerbation or alleviation of various inflammatory diseases. In this review, we discuss the mechanisms by which fibroblasts regulate immune responses by interacting with T cells in host health and diseases, as well as their potential as advanced therapeutic targets.

摘要

成纤维细胞主要被认为是支持器官结构的细胞,目前因其在健康和疾病中调节免疫反应的作用而受到关注。成纤维细胞由于其起源和功能的不同,被赋予了不同的表型和功能。它们在免疫系统中的作用是多方面的,从支持内稳态到诱导或抑制免疫细胞的炎症反应。作为免疫细胞的主要组成部分,T 细胞负责适应性免疫反应,并参与各种炎症性疾病的恶化或缓解。在这篇综述中,我们讨论了成纤维细胞通过与宿主健康和疾病中的 T 细胞相互作用来调节免疫反应的机制,以及它们作为先进治疗靶点的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d515/9868862/02da3f40223c/fimmu-13-1103823-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d515/9868862/c1a89d218acd/fimmu-13-1103823-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d515/9868862/02da3f40223c/fimmu-13-1103823-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d515/9868862/c1a89d218acd/fimmu-13-1103823-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d515/9868862/02da3f40223c/fimmu-13-1103823-g002.jpg

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本文引用的文献

[1]
Immune checkpoint inhibitors as mediators for immunosuppression by cancer-associated fibroblasts: A comprehensive review.

Front Immunol. 2022

[2]
LRRC15 myofibroblasts dictate the stromal setpoint to suppress tumour immunity.

Nature. 2022-11

[3]
Bioinformatic analysis of cancer-associated fibroblast related gene signature as a predictive model in clinical outcomes and immune characteristics of gastric cancer.

Ann Transl Med. 2022-6

[4]
Lymph node fibroblastic reticular cells preserve a tolerogenic niche in allograft transplantation through laminin α4.

J Clin Invest. 2022-7-1

[5]
Mechanisms of joint destruction in rheumatoid arthritis - immune cell-fibroblast-bone interactions.

Nat Rev Rheumatol. 2022-7

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Lymph node fibroblastic reticular cells regulate differentiation and function of CD4 T cells via CD25.

J Exp Med. 2022-5-2

[7]
Crosstalk between cancer-associated fibroblasts and immune cells in the tumor microenvironment: new findings and future perspectives.

Mol Cancer. 2021-10-11

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Importance of lymphocyte-stromal cell interactions in autoimmune and inflammatory rheumatic diseases.

Nat Rev Rheumatol. 2021-9

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Lymph node fibroblastic reticular cells steer immune responses.

Trends Immunol. 2021-8

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Fibroblasts as confederates of the immune system.

Immunol Rev. 2021-7

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