Park Frank
Louisiana State University Health Sciences Center, Department of Medicine, New Orleans, LA 70112, USA.
Hum Gene Ther. 2003 Oct 10;14(15):1489-94. doi: 10.1089/104303403769211691.
Hemophilia A is an inheritable X-linked bleeding disorder most frequently occurring as a consequence of genetic alterations within the factor VIII (FVIII) gene. In the present study, pseudotyped human immunodeficiency virus type 1 (HIV-1)-derived lentivectors expressing hFVIII were assessed for the ability to correct the hemophilia A phenotype in FVIII knockout mice. Therapeutic levels of plasma hFVIII (1-7 ng/mL) were detected in C57B1/6 mice (4-5 weeks old) after portal vein administration of hFVIII-expressing lentivectors pseudotyped with the rhabdoviral vesicular stomatitis viral G protein (VSV-G). More importantly, transduction of hemophilia A mice with FVIII expressing lentivectors resulted in transient correction of the bleeding diathesis phenotype. Moreover, the use of alternate viral pseudotypes based on the lymphocytic choriomeningitis virus (LCMV) resulted in similar circulating levels of FVIII. Interestingly, similar doses of LCMV-pseudotyped lentiviral vectors resulted in minimal systemic or hepatic injury as measured by plasma alanine transferase (ALT), aspartate transferase (AST), and tumor necrosis factor (TNF)-alpha compared to the more commonly used envelope, VSV-G. In summary, these studies demonstrated both the potential merit of lentivectors in terms of correcting monogenic inherited disorders, and also the importance of using alternate pseudotypes, such as LCMV, to safely transfer therapeutic genes in vivo without producing adverse effects.
甲型血友病是一种可遗传的X连锁出血性疾病,最常见的病因是凝血因子VIII(FVIII)基因的遗传改变。在本研究中,对表达人FVIII的1型人类免疫缺陷病毒(HIV-1)衍生的假型慢病毒载体纠正FVIII基因敲除小鼠甲型血友病表型的能力进行了评估。在用弹状病毒水疱性口炎病毒G蛋白(VSV-G)假型化的表达hFVIII的慢病毒载体经门静脉注射后,在4-5周龄的C57B1/6小鼠中检测到了治疗水平的血浆hFVIII(1-7 ng/mL)。更重要的是,用表达FVIII的慢病毒载体转导甲型血友病小鼠导致出血素质表型得到短暂纠正。此外,使用基于淋巴细胞性脉络丛脑膜炎病毒(LCMV)的替代病毒假型导致FVIII的循环水平相似。有趣的是,与更常用的包膜VSV-G相比,相似剂量的LCMV假型慢病毒载体导致血浆丙氨酸转氨酶(ALT)及天冬氨酸转氨酶(AST)和肿瘤坏死因子(TNF)-α所测定的全身或肝脏损伤最小。总之,这些研究证明了慢病毒载体在纠正单基因遗传性疾病方面的潜在价值,以及使用替代假型(如LCMV)在体内安全转移治疗性基因而不产生不良反应的重要性。