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本文引用的文献

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Stability and function of regulatory T cells is maintained by a neuropilin-1-semaphorin-4a axis.调节性 T 细胞的稳定性和功能由神经纤毛蛋白 1-信号素 4a 轴维持。
Nature. 2013 Sep 12;501(7466):252-6. doi: 10.1038/nature12428. Epub 2013 Aug 4.
2
Putting the brakes on anticancer therapies: suppression of innate immune pathways by tumor-associated myeloid cells.抑制抗肿瘤疗法:肿瘤相关髓系细胞对固有免疫通路的抑制作用。
Trends Mol Med. 2013 Sep;19(9):536-45. doi: 10.1016/j.molmed.2013.06.001. Epub 2013 Jun 27.
3
Neutralizing tumor-promoting chronic inflammation: a magic bullet?中和促肿瘤慢性炎症:灵丹妙药?
Science. 2013 Jan 18;339(6117):286-91. doi: 10.1126/science.1232227.
4
TIM-3 as a molecular switch for tumor escape from innate immunity.TIM-3作为肿瘤逃避天然免疫的分子开关。
Front Immunol. 2013 Jan 9;3:418. doi: 10.3389/fimmu.2012.00418. eCollection 2012.
5
TIM family proteins promote the lysosomal degradation of the nuclear receptor NUR77.TIM 家族蛋白促进核受体 NUR77 的溶酶体降解。
Sci Signal. 2012 Dec 11;5(254):ra90. doi: 10.1126/scisignal.2003200.
6
Combined blockade of TIM-3 and TIM-4 augments cancer vaccine efficacy against established melanomas.联合阻断 TIM-3 和 TIM-4 可增强癌症疫苗对已建立的黑色素瘤的疗效。
Cancer Immunol Immunother. 2013 Apr;62(4):629-37. doi: 10.1007/s00262-012-1371-9. Epub 2012 Nov 10.
7
Bat3 promotes T cell responses and autoimmunity by repressing Tim-3–mediated cell death and exhaustion.Bat3 通过抑制 Tim-3 介导的细胞死亡和衰竭来促进 T 细胞反应和自身免疫。
Nat Med. 2012 Sep;18(9):1394-400. doi: 10.1038/nm.2871.
8
Tumor-infiltrating DCs suppress nucleic acid-mediated innate immune responses through interactions between the receptor TIM-3 and the alarmin HMGB1.肿瘤浸润树突状细胞通过 TIM-3 受体与警报素 HMGB1 之间的相互作用抑制核酸介导的固有免疫反应。
Nat Immunol. 2012 Sep;13(9):832-42. doi: 10.1038/ni.2376. Epub 2012 Jul 29.
9
A new development of FG-CC' siRNA blocking interaction of Tim-1 and Tim-4 can enhance DC vaccine against gastric cancer .FG-CC' siRNA阻断Tim-1与Tim-4相互作用的新进展可增强抗胃癌DC疫苗。
Hepatogastroenterology. 2012 Nov-Dec;59(120):2677-82. doi: 10.5754/hge11620.
10
Safety, activity, and immune correlates of anti-PD-1 antibody in cancer.抗 PD-1 抗体在癌症中的安全性、活性和免疫相关性。
N Engl J Med. 2012 Jun 28;366(26):2443-54. doi: 10.1056/NEJMoa1200690. Epub 2012 Jun 2.

TIM 基因家族对肿瘤免疫和免疫抑制的影响。

The impact of the TIM gene family on tumor immunity and immunosuppression.

机构信息

Hokkaido University, Hokkaido, Japan.

Research Center for Infection-Associated Cancer, Institute for Genetic Medicine, Hokkaido University, Hokkaido, Japan.

出版信息

Cell Mol Immunol. 2014 Jan;11(1):41-8. doi: 10.1038/cmi.2013.57. Epub 2013 Dec 16.

DOI:10.1038/cmi.2013.57
PMID:24336162
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4002149/
Abstract

Tumor immunoevasion is an advanced phase of cancer immunosurveillance in which tumor cells acquire the ability to circumvent host immune systems and exploit protumorigenic inflammation. T-cell immunoglobulin mucin (TIM) gene family members have emerged as critical checkpoint proteins that regulate multiple immune response phases and maintain immune homeostasis. Accumulating evidence demonstrates that tumor cells exploit TIM gene family members to evade immunosurveillance, whereas TIM gene family members facilitate the prevention of inflammation-related tumor progression. Thus, a comprehensive analysis to clarify the relative contributions of TIM gene family members in tumor progression may elucidate immunosurveillance systems in cancer patients.

摘要

肿瘤免疫逃逸是癌症免疫监视的一个高级阶段,在此阶段,肿瘤细胞获得了逃避宿主免疫系统和利用促肿瘤炎症的能力。T 细胞免疫球蛋白黏蛋白 (TIM) 基因家族成员已成为关键的检查点蛋白,可调节多种免疫反应阶段并维持免疫稳态。越来越多的证据表明,肿瘤细胞利用 TIM 基因家族成员来逃避免疫监视,而 TIM 基因家族成员则有助于防止与炎症相关的肿瘤进展。因此,全面分析以阐明 TIM 基因家族成员在肿瘤进展中的相对贡献,可能阐明癌症患者的免疫监视系统。