BioMarin Pharmaceutical, Novato, CA, USA.
Department of Pathology, University of California, San Francisco, San Francisco, CA, USA.
Nat Med. 2022 Apr;28(4):789-797. doi: 10.1038/s41591-022-01751-0. Epub 2022 Apr 11.
Factor VIII gene transfer with a single intravenous infusion of valoctocogene roxaparvovec (AAV5-hFVIII-SQ) has demonstrated clinical benefits lasting 5 years to date in people with severe hemophilia A. Molecular mechanisms underlying sustained AAV5-hFVIII-SQ-derived FVIII expression have not been studied in humans. In a substudy of the phase 1/2 clinical trial ( NCT02576795 ), liver biopsy samples were collected 2.6-4.1 years after gene transfer from five participants. Primary objectives were to examine effects on liver histopathology, determine the transduction pattern and percentage of hepatocytes transduced with AAV5-hFVIII-SQ genomes, characterize and quantify episomal forms of vector DNA and quantify transgene expression (hFVIII-SQ RNA and hFVIII-SQ protein). Histopathology revealed no dysplasia, architectural distortion, fibrosis or chronic inflammation, and no endoplasmic reticulum stress was detected in hepatocytes expressing hFVIII-SQ protein. Hepatocytes stained positive for vector genomes, showing a trend for more cells transduced with higher doses. Molecular analysis demonstrated the presence of full-length, inverted terminal repeat-fused, circular episomal genomes, which are associated with long-term expression. Interindividual differences in transgene expression were noted despite similar successful transduction, possibly influenced by host-mediated post-transduction mechanisms of vector transcription, hFVIII-SQ protein translation and secretion. Overall, these results demonstrate persistent episomal vector structures following AAV5-hFVIII-SQ administration and begin to elucidate potential mechanisms mediating interindividual variability.
迄今为止,通过单次静脉输注 valoctocogene roxaparvovec(AAV5-hFVIII-SQ)进行的因子 VIII 基因转移,已在患有严重血友病 A 的人群中显示出持续 5 年的临床益处。尚未在人类中研究持续的 AAV5-hFVIII-SQ 衍生 FVIII 表达的分子机制。在该 1/2 期临床试验的子研究(NCT02576795)中,从 5 名参与者中采集了基因转移后 2.6-4.1 年的肝活检样本。主要目的是检查对肝组织病理学的影响,确定 AAV5-hFVIII-SQ 基因组转导的模式和转导的肝细胞百分比,表征和量化载体 DNA 的附加体形式,并定量转基因表达(hFVIII-SQ RNA 和 hFVIII-SQ 蛋白)。组织病理学显示没有发育不良、结构扭曲、纤维化或慢性炎症,并且在表达 hFVIII-SQ 蛋白的肝细胞中未检测到内质网应激。载体基因组染色阳性,显示出较高剂量转导的细胞更多的趋势。分子分析表明存在全长、反向末端重复融合、圆形附加体基因组,这与长期表达有关。尽管存在类似的成功转导,但在转基因表达方面存在个体间差异,这可能受宿主介导的载体转录、hFVIII-SQ 蛋白翻译和分泌的转导后机制的影响。总的来说,这些结果表明在 AAV5-hFVIII-SQ 给药后持续存在附加体载体结构,并开始阐明介导个体间变异性的潜在机制。