一种用于克服非小细胞肺癌治疗中抗原异质性的多靶向 CAR-T 细胞平台
A Multi-Targeting Chimeric Antigen Receptor-T Cell Platform to Overcome Antigen Heterogeneity in the Treatment of Non-Small Cell Lung Cancer.
这些发现支持采用多靶点CAR-T 策略来应对NSCLC及可能其他实体瘤中的抗原异质性。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Immune responses and immunotherapeutic approaches in the treatment against cancer.
Immune responses and immunotherapeutic approaches in the treatment against cancer.
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由于基因组突变或表观遗传改变,群体内的癌细胞具有异质性。对癌症的免疫反应,尤其是癌症微环境内的 T 细胞库,对癌细胞的控制和生长至关重要。当癌症克隆突破免疫系统的监视时,它就赢得了克服宿主免疫系统的战斗。在这篇综述中,强调了癌症微环境的复杂特征。对癌症免疫反应的分子证据最近已经建立。基于这些免疫与癌症相互作用的分子机制,针对 CTLA-4 和/或 PD-1 对比 PD-L1 的检查点抑制疗法的临床试验已在黑色素瘤、肺癌和其他类型癌症的治疗中取得成功。描述了 T 细胞库的多样性,癌症内的TIL(肿瘤浸润淋巴细胞)可以在体外扩增并回输给患者,作为过继性免疫治疗的一种治疗方式。
Cancer cells within a population are heterogeneous due to genomic mutations or epigenetic changes. The immune response to cancer especially the T cell repertoire within the cancer microenvionment is important to the control and growth of cancer cells. When a cancer clone breaks through the surveillance of the immune system, it wins the battle to overcome the host's immune system. In this review, the complicated profile of the cancer microenvironment is emphasized. The molecular evidence of immune responses to cancer has been recently established.
Based on these molecular mechanisms of immune interactions with cancer, clinical trials based on checkpoint inhibition therapy against CTLA-4 and/or PD-1 versus PD-L1 have been successful in the treatment of melanoma, lung cancer and other types of cancer. The diversity of the T cell repertoire is described and the tumor infiltrating lymphocytes within the cancer may be expanded ex vivo and infused back to the patient as a treatment modality for adoptive immunotherapy.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
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