Scanlan Hayle, Coffman Zachary, Bettencourt Jeffrey, Shipley Timothy, Bramblett Debra E
Rowan School of Medicine, RowanSOM-Jefferson Health-Virtua Our Lady of Lourdes Hospital, Stratford, NJ, United States.
Monroe Clinic Rural Family Medicine Program, The University of Illinois College of Medicine Rockford, Monroe, WI, United States.
Front Oncol. 2022 Jul 27;12:940019. doi: 10.3389/fonc.2022.940019. eCollection 2022.
The need for efficacious and non-toxic cancer therapies is paramount. Oncolytic viruses (OVs) are showing great promise and are introducing new possibilities in cancer treatment with their ability to selectively infect tumor cells and trigger antitumor immune responses. Herpes Simplex Virus 1 (HSV-1) is a commonly selected OV candidate due to its large genome, relative safety profile, and ability to infect a variety of cell types. Talimogene laherparevec (T-VEC) is an HSV-1-derived OV variant and the first and only OV therapy currently approved for clinical use by the United States Food and Drug Administration (FDA). This review provides a concise description of HSV-1 as an OV candidate and the genomic organization of T-VEC. Furthermore, this review focuses on the advantages and limitations in the use of T-VEC compared to other HSV-1 OV variants currently in clinical trials. In addition, approaches for future directions of HSV-1 OVs as cancer therapy is discussed.
对有效且无毒的癌症治疗方法的需求至关重要。溶瘤病毒(OVs)显示出巨大的前景,并凭借其选择性感染肿瘤细胞和触发抗肿瘤免疫反应的能力,为癌症治疗带来了新的可能性。单纯疱疹病毒1型(HSV-1)因其基因组大、相对安全且能感染多种细胞类型,是常用的溶瘤病毒候选物。talimogene laherparevec(T-VEC)是一种源自HSV-1的溶瘤病毒变体,是目前美国食品药品监督管理局(FDA)批准用于临床的首个也是唯一的溶瘤病毒疗法。本综述简要描述了HSV-1作为溶瘤病毒候选物的情况以及T-VEC的基因组结构。此外,本综述重点关注与目前正在进行临床试验的其他HSV-1溶瘤病毒变体相比,使用T-VEC的优势和局限性。此外,还讨论了HSV-1溶瘤病毒作为癌症治疗未来方向的方法。