Laboratory of Molecular Virology, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, 21040-360 Rio de Janeiro, Brazil.
Viruses. 2021 May 2;13(5):822. doi: 10.3390/v13050822.
Immunotherapy has been shown to be highly effective in some types of cancer caused by viruses. Gene therapy involves insertion or modification of a therapeutic gene, to correct for inappropriate gene products that cause/may cause diseases. Both these types of therapy have been used as alternative ways to avoid cancers caused by oncoviruses. In this review, we summarize recent studies on immunotherapy and gene therapy including the topics of oncolytic immunotherapy, immune checkpoint inhibitors, gene replacement, antisense oligonucleotides, RNA interference, clustered regularly interspaced short palindromic repeats Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)-based gene editing, transcription activator-like effector nucleases (TALENs) and custom treatment for Epstein-Barr virus, human T-lymphotropic virus 1, hepatitis B virus, human papillomavirus, hepatitis C virus, herpesvirus associated with Kaposi's sarcoma, Merkel cell polyomavirus, and cytomegalovirus.
免疫疗法已被证明对某些由病毒引起的癌症非常有效。基因疗法涉及插入或修饰治疗基因,以纠正导致/可能导致疾病的不合适的基因产物。这两种类型的疗法都被用作避免致癌病毒的替代方法。在这篇综述中,我们总结了免疫疗法和基因疗法的最新研究,包括溶瘤免疫疗法、免疫检查点抑制剂、基因替换、反义寡核苷酸、RNA 干扰、成簇规律间隔短回文重复序列(CRISPR)的基因编辑、转录激活样效应物核酸酶(TALEN)和针对 Epstein-Barr 病毒、人类 T 淋巴细胞病毒 1、乙型肝炎病毒、人乳头瘤病毒、丙型肝炎病毒、与卡波西肉瘤相关的疱疹病毒、默克尔细胞多瘤病毒和巨细胞病毒的定制治疗。