Lineberger Comprehensive Cancer Center.
Department of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Hum Gene Ther. 2021 Feb;32(3-4):150-157. doi: 10.1089/hum.2020.278.
Chimeric antigen receptor (CAR) T cell therapy has revolutionized the treatment of hematological malignancies, but solid tumors continue to pose significant challenges. Oncolytic viruses (OVs) have generated significant excitement in the field of cancer treatment recently. In particular, OVs can help CAR T cells overcome some of the immunosuppressive mechanisms within the tumor microenvironment through OV intrinsic effects or delivery of immunostimulatory agents. Numerous preclinical studies demonstrate that combining CAR T cells with OVs can increase CAR T cell trafficking, antitumor activity, and elimination of antigen-negative tumor cells. Despite promising preclinical results, only one clinical trial (NCT03740256) investigating CAR T and OV combination therapy is underway, highlighting the challenges of translating this approach to the clinic. Antiviral immunity and the route of OV administration, in addition to concerns about cost and safety, limit the clinical application of this approach. Strategies to reduce the production cost of both CAR T cells and OVs, as well as molecularly modifying OVs to enhance their bioavailability, will likely encourage further exploration of this combination therapy in clinical trials.
嵌合抗原受体 (CAR) T 细胞疗法已经彻底改变了血液系统恶性肿瘤的治疗方法,但实体瘤仍然是一个重大的挑战。溶瘤病毒 (OVs) 最近在癌症治疗领域引起了广泛关注。特别是,OVs 可以通过 OV 内在作用或递送免疫刺激剂,帮助 CAR T 细胞克服肿瘤微环境中的一些免疫抑制机制。大量的临床前研究表明,将 CAR T 细胞与 OV 联合使用可以增加 CAR T 细胞的迁移、抗肿瘤活性,并消除抗原阴性的肿瘤细胞。尽管有很有前景的临床前结果,但目前只有一项临床试验(NCT03740256)正在研究 CAR T 和 OV 联合治疗,这凸显了将这种方法转化为临床应用的挑战。抗病毒免疫和 OV 的给药途径,以及对成本和安全性的担忧,限制了这种方法的临床应用。降低 CAR T 细胞和 OV 的生产成本的策略,以及对 OV 进行分子修饰以提高其生物利用度,可能会鼓励在临床试验中进一步探索这种联合治疗。