决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Oncolytic ImmunoViroTherapy: A long history of crosstalk between viruses and immune system for cancer treatment.
肿瘤免疫治疗依赖于调动患者的免疫系统,以精细调控特异性抗肿瘤应答并最终清除肿瘤。
癌症免疫治疗依赖利用患者自身免疫系统,精细调节特异性抗肿瘤应答并最终清除癌症。在多种治疗方法中,溶瘤病毒(OV)已成为一种新型癌症免疫疗法。OV是一类天然存在或经基因改造的病毒,能够选择性杀伤癌细胞而不损伤健康细胞;过去20年中,其作用已不再局限于溶瘤活性。事实上,OV介导的免疫原性癌细胞死亡可诱导肿瘤抗原释放,继而引发抗肿瘤免疫,使OV成为原位治疗性癌症疫苗。此外,还可对OV进行工程化改造,使其向肿瘤内递送肿瘤抗原或细胞因子等免疫刺激分子,进一步增强抗肿瘤应答。OV还可与免疫检查点抑制剂、CAR-T细胞等其他癌症免疫疗法联合使用。本综述首先介绍当前癌症治疗所用OV的三种主要作用机制(MOA):i)溶瘤;ii)OV诱导的癌症特异性免疫激活;iii)利用既存抗病毒免疫增强癌症治疗。其次,重点讨论OV如何以特异或非特异方式诱导和/或增强抗癌免疫,并阐明这些方法的重要性。最后,分析OV与其他癌症免疫疗法联合使用,回顾目前和未来的临床应用。
Cancer Immunotherapy relies on harnessing a patient's immune system to fine-tune specific anti-tumor responses and ultimately eradicate cancer. Among diverse therapeutic approaches, oncolytic viruses (OVs) have emerged as a novel form of cancer immunotherapy. OVs are a naturally occurring or genetically modified class of viruses able to selectively kill cancer cells, leaving healthy cells unharmed; in the last two decades, the role of OVs has been redefined to act beyond their oncolytic activity. Indeed, the immunogenic cancer cell death mediated by OVs induces the release of tumor antigens that in turn induces anti-tumor immunity, allowing OVs to act as in situ therapeutic cancer vaccines. Additionally, OVs can be engineered for intratumoral delivery of immunostimulatory molecules such as tumor antigens or cytokines to further enhance anti-tumor response. Moreover, OVs can be used in combination with other cancer immunotherapeutic approaches such as Immune Checkpoint Inhibitors and CAR-T cells. The current review first defines the three main mechanisms of action (MOA) of OVs currently used in cancer therapy that are: i) Oncolysis, ii) OV-induced cancer-specific immune activation, and iii) Exploiting pre-existing anti-viral immunity to enhance cancer therapy. Secondly, we focus on how OVs can induce and/or improve anti-cancer immunity in a specific or unspecific fashion, highlighting the importance of these approaches. Finally, the last part of the review analyses OVs combined with other cancer immunotherapies, revising present and future clinical applications.
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