California Pacific Medical Center and Research Institute, University of California School of Medicine, San Francisco, USA.
Clin Exp Metastasis. 2024 Aug;41(4):473-493. doi: 10.1007/s10585-024-10300-7. Epub 2024 Aug 18.
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.
由于基因组突变或表观遗传改变,肿瘤细胞在群体内存在异质性。机体对肿瘤的免疫反应,尤其是肿瘤微环境中的 T 细胞库,对控制和肿瘤细胞生长至关重要。当肿瘤克隆突破免疫系统的监测时,它就赢得了与宿主免疫系统斗争的胜利。在这篇综述中,强调了肿瘤微环境的复杂特征。最近已经确定了针对肿瘤的免疫反应的分子证据。基于这些免疫相互作用与癌症的分子机制,针对 CTLA-4 和/或 PD-1 与 PD-L1 的检查点抑制治疗的临床试验在黑色素瘤、肺癌和其他类型的癌症治疗中取得了成功。描述了 T 细胞库的多样性,并且可以在体外扩增肿瘤浸润淋巴细胞,并将其作为过继免疫疗法回输给患者。