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CD8 调节性 T 细胞在免疫耐受中的未来前景。

Future prospects for CD8 regulatory T cells in immune tolerance.

机构信息

Centre de Recherche en Transplantation et Immunologie UMR 1064, INSERM, Université de Nantes, Nantes, France.

Institut de Transplantation Urologie Néphrologie (ITUN), CHU Nantes, Nantes, France.

出版信息

Immunol Rev. 2019 Nov;292(1):209-224. doi: 10.1111/imr.12812. Epub 2019 Oct 8.

DOI:10.1111/imr.12812
PMID:31593314
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7027528/
Abstract

CD8 Tregs have been long described and significant progresses have been made about their phenotype, their functional mechanisms, and their suppressive ability compared to conventional CD4 Tregs. They are now at the dawn of their clinical use. In this review, we will summarize their phenotypic characteristics, their mechanisms of action, the similarities, differences and synergies between CD8 and CD4 Tregs, and we will discuss the biology, development and induction of CD8 Tregs, their manufacturing for clinical use, considering open questions/uncertainties and future technically accessible improvements notably through genetic modifications.

摘要

CD8 Tregs 已经被长期描述,并且在其表型、功能机制和与传统 CD4 Tregs 相比的抑制能力方面取得了重大进展。它们现在正处于临床应用的曙光阶段。在这篇综述中,我们将总结它们的表型特征、作用机制、CD8 和 CD4 Tregs 之间的相似性、差异和协同作用,我们将讨论 CD8 Tregs 的生物学、发育和诱导,以及它们用于临床应用的制造,考虑到开放性问题/不确定性和未来通过遗传修饰等技术上可实现的改进。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7f7/7027528/56742cb6db48/IMR-292-209-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7f7/7027528/93a10c203ac5/IMR-292-209-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7f7/7027528/56742cb6db48/IMR-292-209-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7f7/7027528/93a10c203ac5/IMR-292-209-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7f7/7027528/56742cb6db48/IMR-292-209-g002.jpg

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Cell Death Dis. 2019 May 28;10(6):407. doi: 10.1038/s41419-019-1642-x.
3
T-cell exhaustion correlates with improved outcomes in kidney transplant recipients.
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Front Immunol. 2025 Apr 16;16:1574327. doi: 10.3389/fimmu.2025.1574327. eCollection 2025.
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Synthetic rEg.P29 Peptides Induce Protective Immune Responses Against in Mice.合成的重组P29肽诱导小鼠针对[具体疾病或病原体,原文未明确]产生保护性免疫反应。
Vaccines (Basel). 2025 Mar 3;13(3):266. doi: 10.3390/vaccines13030266.
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Low-dose interleukin 2 therapy halts the progression of post-streptococcal autoimmune complications in a rat model of rheumatic heart disease.低剂量白细胞介素2疗法可阻止风湿性心脏病大鼠模型中链球菌感染后自身免疫并发症的进展。
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