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Back from the dead: TIL apoptosis in cancer immune evasion.

作者信息

Horton Brendan L, Gajewski Thomas F

机构信息

Department of Pathology, University of Chicago, Chicago, IL, USA.

出版信息

Br J Cancer. 2018 Feb 6;118(3):309-311. doi: 10.1038/bjc.2017.483. Epub 2018 Jan 23.

DOI:10.1038/bjc.2017.483
PMID:29360810
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5808044/
Abstract
摘要

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Back from the dead: TIL apoptosis in cancer immune evasion.起死回生:肿瘤浸润淋巴细胞凋亡与肿瘤免疫逃逸
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Oncotarget. 2016 Feb 16;7(7):7390-402. doi: 10.18632/oncotarget.7180.
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Tumor specific cytolysis by tumor infiltrating lymphocytes in breast cancer.乳腺癌中肿瘤浸润淋巴细胞介导的肿瘤特异性细胞溶解作用。
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CD20+ tumor-infiltrating lymphocytes have an atypical CD27- memory phenotype and together with CD8+ T cells promote favorable prognosis in ovarian cancer.CD20+ 肿瘤浸润淋巴细胞具有非典型的 CD27- 记忆表型,与 CD8+ T 细胞一起促进卵巢癌的预后良好。
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Adhesion analysis via a tumor vasculature-like microfluidic device identifies CD8 T cells with enhanced tumor homing to improve cell therapy.通过一种类似于肿瘤血管的微流控装置进行黏附分析,鉴定出具有增强肿瘤归巢能力的 CD8 T 细胞,从而改善细胞治疗效果。
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本文引用的文献

1
Resistance to cancer immunotherapy mediated by apoptosis of tumor-infiltrating lymphocytes.肿瘤浸润淋巴细胞凋亡介导的癌症免疫治疗抵抗。
Nat Commun. 2017 Nov 10;8(1):1404. doi: 10.1038/s41467-017-00784-1.
2
Intratumoral CD8 T-cell Apoptosis Is a Major Component of T-cell Dysfunction and Impedes Antitumor Immunity.肿瘤内 CD8 T 细胞凋亡是 T 细胞功能障碍的主要组成部分,并阻碍抗肿瘤免疫。
Cancer Immunol Res. 2018 Jan;6(1):14-24. doi: 10.1158/2326-6066.CIR-17-0249. Epub 2017 Nov 2.
3
The EGR2 targets LAG-3 and 4-1BB describe and regulate dysfunctional antigen-specific CD8+ T cells in the tumor microenvironment.
实体瘤中免疫检查点抑制剂作用的多级机制:历史、当前问题及未来发展
Oncol Lett. 2022 Jun;23(6):190. doi: 10.3892/ol.2022.13310. Epub 2022 Apr 29.
4
Programmed Cell Death Tunes Tumor Immunity.程序性细胞死亡调节肿瘤免疫。
Front Immunol. 2022 Mar 30;13:847345. doi: 10.3389/fimmu.2022.847345. eCollection 2022.
5
Signatures of CD8+ T cell dysfunction in AML patients and their reversibility with response to chemotherapy.AML 患者 CD8+T 细胞功能障碍的特征及其对化疗反应的可逆性。
JCI Insight. 2018 Nov 2;3(21):120974. doi: 10.1172/jci.insight.120974.
EGR2靶向LAG-3和4-1BB描述并调节肿瘤微环境中功能失调的抗原特异性CD8 + T细胞。
J Exp Med. 2017 Feb;214(2):381-400. doi: 10.1084/jem.20160485. Epub 2017 Jan 23.
4
Density of immunogenic antigens does not explain the presence or absence of the T-cell-inflamed tumor microenvironment in melanoma.免疫原性抗原的密度并不能解释黑色素瘤中T细胞炎症性肿瘤微环境的存在与否。
Proc Natl Acad Sci U S A. 2016 Nov 29;113(48):E7759-E7768. doi: 10.1073/pnas.1609376113. Epub 2016 Nov 11.
5
Tumor immune profiling predicts response to anti-PD-1 therapy in human melanoma.肿瘤免疫谱分析可预测人类黑色素瘤对抗PD-1治疗的反应。
J Clin Invest. 2016 Sep 1;126(9):3447-52. doi: 10.1172/JCI87324. Epub 2016 Aug 15.
6
Innate and adaptive immune cells in the tumor microenvironment.肿瘤微环境中的固有和适应性免疫细胞。
Nat Immunol. 2013 Oct;14(10):1014-22. doi: 10.1038/ni.2703.
7
Human melanoma-specific CD8(+) T-cells from metastases are capable of antigen-specific degranulation and cytolysis directly ex vivo.转移性黑色素瘤患者的特异性 CD8(+) T 细胞能够直接在体外进行抗原特异性脱颗粒和细胞溶解。
Oncoimmunology. 2012 Jul 1;1(4):467-530. doi: 10.4161/onci.19856.
8
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.
9
Improved survival with ipilimumab in patients with metastatic melanoma.Ipilimumab 改善转移性黑色素瘤患者的生存。
N Engl J Med. 2010 Aug 19;363(8):711-23. doi: 10.1056/NEJMoa1003466. Epub 2010 Jun 5.