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Immune-resistant mechanisms in cancer immunotherapy.
International Journal of Clinical Oncology ( IF 2.4 ) Pub Date : 2020-01-09 , DOI: 10.1007/s10147-019-01611-x
Yutaka Kawakami 1, 2 , Shigeki Ohta 2 , Mohammad A Sayem 2 , Nobuo Tsukamoto 2 , Tomonori Yaguchi 2
Affiliation  

Immune checkpoint inhibitors (ICI) such as PD-1/PD-L1 antibodies (Abs) and CTLA4 Abs and T cell-based adoptive cell therapies are effective for patients with various cancers. However, response rates of ICI monotherapies are still limited due to lack of immunogenic antigens and various immune-resistant mechanisms. The latter includes adaptive immune resistance that is caused by anti-tumor T cells (e.g. PD-L1 induced by IFN-γ from T cells) and primary immune resistance that is caused by cancer cells (e.g. immunosuppressive cytokines produced by cancer cells). Further understanding of the immune-resistant mechanisms, which may be possible through comparative analyses of responders and non-responders to the immunotherapies, will lead to the identification of new diagnostic biomarkers and therapeutic targets for development of effective cancer immuno therapies.

中文翻译:

癌症免疫治疗中的免疫抵抗机制。

免疫检查点抑制剂(ICI),例如PD-1 / PD-L1抗体(Abs)和CTLA4 Abs和基于T细胞的过继细胞疗法对各种癌症患者均有效。但是,由于缺乏免疫原性抗原和各种免疫抵抗机制,ICI单一疗法的应答率仍然受到限制。后者包括由抗肿瘤T细胞(例如,由T细胞的IFN-γ诱导的PD-L1)引起的适应性免疫抗性和由癌细胞(例如,癌细胞产生的免疫抑制细胞因子)引起的原发性免疫抗性。通过对免疫疗法的反应者和非反应者进行比较分析,可能进一步了解免疫抵抗机制,
更新日期:2020-01-09
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