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Strategies for combining immunotherapy with radiation for anticancer therapy.免疫疗法与放射疗法联合用于抗癌治疗的策略。
Immunotherapy. 2015;7(9):967-980. doi: 10.2217/imt.15.65. Epub 2015 Aug 27.
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Chimeric antigen receptor engineering: a right step in the evolution of adoptive cellular immunotherapy.嵌合抗原受体工程:过继细胞免疫治疗进化过程中的正确步骤。
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Challenges of cancer therapy with natural killer cells.自然杀伤细胞用于癌症治疗的挑战。
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[Immune-checkpoints: the new anti-cancer immunotherapies].[免疫检查点:新型抗癌免疫疗法]
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本文引用的文献

1
Radiation and dual checkpoint blockade activate non-redundant immune mechanisms in cancer.放疗和双重检查点阻断激活癌症中的非冗余免疫机制。
Nature. 2015 Apr 16;520(7547):373-7. doi: 10.1038/nature14292. Epub 2015 Mar 9.
2
Growth inhibitory effects of miR-221 and miR-222 in non-small cell lung cancer cells.miR-221和miR-222对非小细胞肺癌细胞的生长抑制作用。
Cancer Med. 2015 Apr;4(4):551-64. doi: 10.1002/cam4.412. Epub 2015 Jan 30.
3
Designing chimeric antigen receptors to effectively and safely target tumors.设计嵌合抗原受体以有效且安全地靶向肿瘤。
Curr Opin Immunol. 2015 Apr;33:9-15. doi: 10.1016/j.coi.2015.01.002. Epub 2015 Jan 23.
4
NK cells and T cells cooperate during the clinical course of colorectal cancer.自然杀伤细胞和 T 细胞在结直肠癌的临床病程中协同作用。
Oncoimmunology. 2014 Aug 3;3(8):e952197. doi: 10.4161/21624011.2014.952197. eCollection 2014.
5
Effector T cells boost regulatory T cell expansion by IL-2, TNF, OX40, and plasmacytoid dendritic cells depending on the immune context.效应T细胞根据免疫环境,通过白细胞介素-2、肿瘤坏死因子、OX40和浆细胞样树突状细胞促进调节性T细胞的扩增。
J Immunol. 2015 Feb 1;194(3):999-1010. doi: 10.4049/jimmunol.1400504. Epub 2014 Dec 29.
6
Predictive correlates of response to the anti-PD-L1 antibody MPDL3280A in cancer patients.癌症患者对抗PD-L1抗体MPDL3280A反应的预测性相关因素。
Nature. 2014 Nov 27;515(7528):563-7. doi: 10.1038/nature14011.
7
MPDL3280A (anti-PD-L1) treatment leads to clinical activity in metastatic bladder cancer.MPDL3280A(抗 PD-L1)治疗可导致转移性膀胱癌的临床活性。
Nature. 2014 Nov 27;515(7528):558-62. doi: 10.1038/nature13904.
8
Genetic basis for clinical response to CTLA-4 blockade in melanoma.黑色素瘤中CTLA-4阻断临床反应的遗传基础。
N Engl J Med. 2014 Dec 4;371(23):2189-2199. doi: 10.1056/NEJMoa1406498. Epub 2014 Nov 19.
9
Radiation-induced matrix metalloproteinases limit natural killer cell-mediated anticancer immunity in NCI-H23 lung cancer cells.辐射诱导的基质金属蛋白酶限制了自然杀伤细胞介导的对NCI-H23肺癌细胞的抗癌免疫。
Mol Med Rep. 2015 Mar;11(3):1800-6. doi: 10.3892/mmr.2014.2918. Epub 2014 Nov 10.
10
Effect of neoadjuvant chemoradiation on tumor-infiltrating/associated lymphocytes in locally advanced rectal cancers.新辅助放化疗对局部晚期直肠癌肿瘤浸润/相关淋巴细胞的影响。
Anticancer Res. 2014 Nov;34(11):6505-13.

免疫疗法与放射疗法联合用于抗癌治疗的策略。

Strategies for combining immunotherapy with radiation for anticancer therapy.

作者信息

Seyedin Steven N, Schoenhals Jonathan E, Lee Dean A, Cortez Maria A, Wang Xiaohong, Niknam Sharareh, Tang Chad, Hong David S, Naing Aung, Sharma Padmanee, Allison James P, Chang Joe Y, Gomez Daniel R, Heymach John V, Komaki Ritsuko U, Cooper Laurence J, Welsh James W

机构信息

Department of Radiation Oncology, University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX 77030, USA.

Department of Experimental Radiation Oncology, University of Texas MD Anderson Cancer Center, TX, USA.

出版信息

Immunotherapy. 2015;7(9):967-980. doi: 10.2217/imt.15.65. Epub 2015 Aug 27.

DOI:10.2217/imt.15.65
PMID:26310908
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4825325/
Abstract

Radiation therapy controls local disease but also prompts the release of tumor-associated antigens and stress-related danger signals that primes T cells to promote tumor regression at unirradiated sites known as the abscopal effect. This may be enhanced by blocking inhibitory immune signals that modulate immune activity through a variety of mechanisms. Indeed, abscopal responses have occurred in patients with lung cancer or melanoma when given anti-CTLA4 antibody and radiation. Other approaches involve expanding and reinfusing T or NK cells or engineered T cells to express receptors that target specific tumor peptides. These approaches may be useful for immunocompromised patients receiving radiation. Preclinical and clinical studies are testing both immune checkpoint-based strategies and adoptive immunotherapies with radiation.

摘要

放射治疗可控制局部疾病,但也会促使肿瘤相关抗原和应激相关危险信号的释放,这些信号会使T细胞致敏,从而促进未受照射部位的肿瘤消退,即所谓的远隔效应。通过阻断通过多种机制调节免疫活性的抑制性免疫信号,这一效应可能会增强。事实上,肺癌或黑色素瘤患者在接受抗CTLA4抗体和放射治疗时会出现远隔反应。其他方法包括扩增和回输T细胞或NK细胞,或改造T细胞以表达靶向特定肿瘤肽的受体。这些方法可能对接受放疗的免疫功能低下患者有用。临床前和临床研究正在测试基于免疫检查点的策略以及放疗联合过继性免疫疗法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a47/4825325/eb679308a1fc/nihms-770390-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a47/4825325/eb679308a1fc/nihms-770390-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a47/4825325/eb679308a1fc/nihms-770390-f0001.jpg