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调节性 T 细胞:免疫平衡的掌控者和未来治疗创新的源泉。

Regulatory T cells: masterminds of immune equilibrium and future therapeutic innovations.

机构信息

Department of Tumor Biological Treatment, The Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu, China.

Jiangsu Engineering Research Center for Tumor Immunotherapy, The Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu, China.

出版信息

Front Immunol. 2024 Sep 3;15:1457189. doi: 10.3389/fimmu.2024.1457189. eCollection 2024.


DOI:10.3389/fimmu.2024.1457189
PMID:39290699
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11405253/
Abstract

Regulatory T cells (Tregs), a subset of CD4T cells marked by the expression of the transcription factor forkhead box protein 3 (Foxp3), are pivotal in maintaining immune equilibrium and preventing autoimmunity. In our review, we addressed the functional distinctions between Foxp3Tregs and other T cells, highlighting their roles in autoimmune diseases and cancer. We uncovered the dual nature of Tregs: they prevented autoimmune diseases by maintaining self-tolerance while contributing to tumor evasion by suppressing anti-tumor immunity. This study underscored the potential for targeted therapeutic strategies, such as enhancing Treg activity to restore balance in autoimmune diseases or depleting Foxp3Tregs to augment anti-tumor immune responses in cancer. These insights laid the groundwork for future research and clinical applications, emphasizing the critical role of Foxp3Tregs in immune regulation and the advancement of next-generation immunotherapies.

摘要

调节性 T 细胞(Tregs)是 CD4T 细胞的一个亚群,其特征是表达转录因子叉头框蛋白 3(Foxp3)。它们在维持免疫平衡和预防自身免疫中起着关键作用。在我们的综述中,我们探讨了 Foxp3Tregs 和其他 T 细胞之间的功能区别,强调了它们在自身免疫性疾病和癌症中的作用。我们揭示了 Tregs 的双重性质:它们通过维持自身耐受来预防自身免疫性疾病,同时通过抑制抗肿瘤免疫来促进肿瘤逃逸。这项研究强调了靶向治疗策略的潜力,例如增强 Treg 活性以恢复自身免疫性疾病中的平衡,或耗尽 Foxp3Tregs 以增强癌症中的抗肿瘤免疫反应。这些见解为未来的研究和临床应用奠定了基础,强调了 Foxp3Tregs 在免疫调节和下一代免疫疗法中的关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1333/11405253/63ac73ccd1fb/fimmu-15-1457189-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1333/11405253/e0d120ae7ae5/fimmu-15-1457189-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1333/11405253/b2a314866c3d/fimmu-15-1457189-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1333/11405253/63ac73ccd1fb/fimmu-15-1457189-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1333/11405253/e0d120ae7ae5/fimmu-15-1457189-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1333/11405253/b2a314866c3d/fimmu-15-1457189-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1333/11405253/63ac73ccd1fb/fimmu-15-1457189-g003.jpg

相似文献

[1]
Regulatory T cells: masterminds of immune equilibrium and future therapeutic innovations.

Front Immunol. 2024

[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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本文引用的文献

[1]
Induction of regulatory T cells and efficacy of low-dose interleukin-2 in systemic sclerosis: interventional open-label phase 1-phase 2a study.

RMD Open. 2024-4-4

[2]
Gedatolisib in combination with palbociclib and endocrine therapy in women with hormone receptor-positive, HER2-negative advanced breast cancer: results from the dose expansion groups of an open-label, phase 1b study.

Lancet Oncol. 2024-4

[3]
Metabolic targeting of cancer associated fibroblasts overcomes T-cell exclusion and chemoresistance in soft-tissue sarcomas.

Nat Commun. 2024-3-20

[4]
A humanized IL-2 mutein expands Tregs and prolongs transplant survival in preclinical models.

J Clin Invest. 2024-3-1

[5]
Anti-TIGIT antibody improves PD-L1 blockade through myeloid and T cells.

Nature. 2024-3

[6]
INHBA(+) cancer-associated fibroblasts generate an immunosuppressive tumor microenvironment in ovarian cancer.

NPJ Precis Oncol. 2024-2-15

[7]
Triggers for the onset and recurrence of psoriasis: a review and update.

Cell Commun Signal. 2024-2-12

[8]
Individualised neoantigen therapy mRNA-4157 (V940) plus pembrolizumab versus pembrolizumab monotherapy in resected melanoma (KEYNOTE-942): a randomised, phase 2b study.

Lancet. 2024-2-17

[9]
Immune cells in the epithelial immune microenvironment of psoriasis: emerging therapeutic targets.

Front Immunol. 2023

[10]
Strengthening bonds via RyR2 inhibition helps immune suppression.

J Clin Invest. 2023-12-15

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