MRC/UCL Centre for Medical Molecular Virology and Wohl Virion Centre, Division of Infection & Immunity, UCL Cancer Institute, University College London, London, UK.
Curr Gene Ther. 2013 Jun 1;13(3):211-27. doi: 10.2174/1566523211313030006.
Retroviral vectors derived from gammaretroviruses or lentiviruses have now been used extensively in clinical gene therapy trials for several diseases including primary immunodeficiencies, beta thalassaemia and adrenoleukodystrophy. Their utility in this setting has been readily demonstrated by the largely favourable outcomes in recent clinical trials, however this success has been marred by the emergence of malignancies in some trials. These malignancies were a consequence of perturbation of cellular proto-oncogene expression by the integrated retroviral vectors, the process of which is referred to as 'insertional mutagenesis' (IM). In this review, the origins of our understanding of IM are reviewed and applied to the clinical gene therapy trials conducted with retroviral vectors. Old and new methods for assessing this phenomenon are discussed with a view to provide a comprehensive account of this emerging field.
逆转录病毒载体来源于γ逆转录病毒或慢病毒,现已广泛应用于多种疾病的临床基因治疗试验,包括原发性免疫缺陷、β地中海贫血和肾上腺脑白质营养不良。最近的临床试验结果大多较为乐观,这充分证明了它们在这方面的实用性,但一些试验中出现的恶性肿瘤也给这一成功蒙上了阴影。这些恶性肿瘤是整合的逆转录病毒载体干扰细胞原癌基因表达的结果,这一过程被称为“插入突变”(IM)。在这篇综述中,我们回顾了对 IM 的理解的起源,并将其应用于使用逆转录病毒载体进行的临床基因治疗试验。讨论了评估这种现象的旧方法和新方法,以期全面阐述这一新兴领域。