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Tim-3在母胎耐受中的作用:当前认识综述

Involvement of Tim-3 in Maternal-fetal Tolerance: A Review of Current Understanding.

作者信息

Meng Xinhang, Luo Yujie, Cui Liyuan, Wang Songcun

机构信息

Laboratory for Reproductive Immunology, Hospital of Obstetrics and Gynecology, Fudan University Shanghai Medical College, Shanghai 200011, China.

出版信息

Int J Biol Sci. 2025 Jan 1;21(2):789-801. doi: 10.7150/ijbs.106115. eCollection 2025.

DOI:10.7150/ijbs.106115
PMID:39781467
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11705645/
Abstract

As the first T cell immunoglobulin mucin (Tim) family member to be identified, Tim-3 is a powerful immune checkpoint that functions in immunoregulation and induction of tolerance. Conventionally, Tim-3 is considered to play a role in adaptive immunity, especially in helper T cell-mediated immune responses. As researches progress, Tim-3 has been detected in a wider range of cell types, modulating cell function through ligand-receptor interactions and other pathways. Strikingly, Tim-3 plays a pivotal role in maternal-fetal tolerance by regulating immune cell functions and orchestrating the maternal-fetal cross-talk. In this review, we elaborate on the involvement of Tim-3 in immunology, with a focus on its participation in maternal-fetal tolerance to provide new insights into immunoregulation during pregnancy. Our work will be helpful in further understanding the pathogenesis of pregnancy-related diseases and will inspire new strategies for their diagnosis and treatment.

摘要

作为首个被鉴定出的T细胞免疫球蛋白黏蛋白(Tim)家族成员,Tim-3是一种强大的免疫检查点,在免疫调节和诱导免疫耐受中发挥作用。传统上,Tim-3被认为在适应性免疫中发挥作用,尤其是在辅助性T细胞介导的免疫反应中。随着研究的进展,Tim-3已在更广泛的细胞类型中被检测到,通过配体-受体相互作用和其他途径调节细胞功能。引人注目的是,Tim-3通过调节免疫细胞功能和协调母胎对话,在母胎耐受中发挥关键作用。在本综述中,我们阐述了Tim-3在免疫学中的参与情况,重点关注其在母胎耐受中的作用,为孕期免疫调节提供新的见解。我们的工作将有助于进一步了解妊娠相关疾病的发病机制,并为其诊断和治疗激发新的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c6c/11705645/c6eb8330c744/ijbsv21p0789g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c6c/11705645/6ab491d2f518/ijbsv21p0789g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c6c/11705645/ef45eb3ef290/ijbsv21p0789g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c6c/11705645/c6eb8330c744/ijbsv21p0789g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c6c/11705645/6ab491d2f518/ijbsv21p0789g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c6c/11705645/ef45eb3ef290/ijbsv21p0789g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c6c/11705645/c6eb8330c744/ijbsv21p0789g003.jpg

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本文引用的文献

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IL-27/Blimp-1 axis regulates the differentiation and function of Tim-3+ Tregs during early pregnancy.IL-27/Blimp-1 轴调节妊娠早期 Tim-3+Tregs 的分化和功能。
JCI Insight. 2024 Aug 22;9(16):e179233. doi: 10.1172/jci.insight.179233.
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Soluble Tim-3 serves as a tumor prognostic marker and therapeutic target for CD8 T cell exhaustion and anti-PD-1 resistance.可溶性 Tim-3 可作为肿瘤预后标志物,并可作为耗尽的 CD8 T 细胞及抗 PD-1 耐药的治疗靶点。
Cell Rep Med. 2024 Aug 20;5(8):101686. doi: 10.1016/j.xcrm.2024.101686.
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TOX2 nuclear-cytosol translocation is linked to leukemogenesis of acute T-cell leukemia by repressing TIM3 transcription.
TOX2 的核质易位通过抑制 TIM3 转录与急性 T 细胞白血病的白血病发生有关。
Cell Death Differ. 2024 Nov;31(11):1506-1518. doi: 10.1038/s41418-024-01352-z. Epub 2024 Jul 30.
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TIM-3 Expression on Dendritic Cells in Colorectal Cancer.结直肠癌中树突状细胞上TIM-3的表达
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J Transl Int Med. 2024 Mar 21;12(1):96-105. doi: 10.2478/jtim-2023-0104. eCollection 2024 Feb.
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