Ban Weiyue, Guan Jianhuan, Huang Hanwei, He Zhonggui, Sun Mengchi, Liu Funan, Sun Jin
Wuya College of Innovation, Shenyang Pharmaceutical University, Shenyang, 110016 China.
Department of Surgical Oncology and General Surgery, The First Hospital of China Medical University; Key Laboratory of Precision Diagnosis and Treatment of Gastrointestinal Tumors, China Medical University, Ministry of Education, Shenyang, 110016 China.
Nano Res. 2022;15(5):4137-4153. doi: 10.1007/s12274-021-4031-6. Epub 2022 Feb 14.
Oncolytic virotherapy (OVT) is a novel type of immunotherapy that induces anti-tumor responses through selective self-replication within cancer cells and oncolytic virus (OV)-mediated immunostimulation. Notably, talimogene laherparepvec (T-Vec) developed by the Amgen company in 2015, is the first FDA-approved OV product to be administered via intratumoral injection and has been the most successful OVT treatment. However, the systemic administration of OVs still faces huge challenges, including pre-existing neutralizing antibodies and poor targeting delivery efficacy. Recently, state-of-the-art progress has been made in the development of systemic delivery of OVs, which demonstrates a promising step toward broadening the scope of cancer immunotherapy and improving the clinical efficacy of OV delivery. Herein, this review describes the general characteristics of OVs, focusing on the action mechanisms of OVs as well as the advantages and disadvantages of OVT. The emerging multiple systemic administration approaches of OVs are summarized in the past five years. In addition, the combination treatments between OVT and traditional therapies (chemotherapy, thermotherapy, immunotherapy, and radiotherapy, etc.) are highlighted. Last but not least, the future prospects and challenges of OVT are also discussed, with the aim of facilitating medical researchers to extensively apply the OVT in the cancer therapy.
溶瘤病毒疗法(OVT)是一种新型免疫疗法,通过在癌细胞内选择性自我复制以及溶瘤病毒(OV)介导的免疫刺激来诱导抗肿瘤反应。值得注意的是,安进公司于2015年研发的talimogene laherparepvec(T-Vec)是首个获美国食品药品监督管理局(FDA)批准通过瘤内注射给药的OV产品,并且是最成功的OVT治疗方法。然而,OV的全身给药仍面临巨大挑战,包括预先存在的中和抗体以及靶向递送效果不佳。最近,在OV全身递送的研发方面取得了前沿进展,这朝着拓宽癌症免疫疗法范围以及提高OV递送的临床疗效迈出了有希望的一步。在此,本综述描述了OV的一般特征,重点关注OV的作用机制以及OVT的优缺点。总结了过去五年中出现的多种OV全身给药方法。此外,还强调了OVT与传统疗法(化疗、热疗、免疫疗法和放射疗法等)之间的联合治疗。最后但同样重要的是,还讨论了OVT的未来前景和挑战,旨在促进医学研究人员在癌症治疗中广泛应用OVT。