Dinauer M C, Li L L, Björgvinsdóttir H, Ding C, Pech N
Herman B Wells Center for Pediatric Research, Departments of Pediatrics (Hematology/Oncology) and Medical and Molecular Genetics, James Whitcomb Riley Hospital for Children, Indiana University School of Medicine, Indianapolis, IN, USA.
Blood. 1999 Aug 1;94(3):914-22.
Chronic granulomatous disease (CGD) is an inherited deficiency of the superoxide-generating phagocyte nicotinamide adenine dinucleotide phosphate (NADPH) oxidase, resulting in recurrent, severe bacterial and fungal infections. The X-linked form of this disorder (X-CGD) results from mutations in the X-linked gene for gp91(phox), the larger subunit of the oxidase flavocytochrome b(558). In this study, we used a murine model of X-CGD to examine the long-term function of retroviral vectors for expression of gp91(phox) based on the murine stem cell virus (MSCV) backbone. NADPH oxidase activity was reconstituted in neutrophils and macrophages for up to 18 to 24 months posttransplantation of transduced X-CGD bone marrow into lethally irradiated syngeneic X-CGD mice. Southern blot analysis and secondary transplant data showed proviral integration in multilineage repopulating cells. Although relatively small amounts of recombinant gp91(phox) (approximately 5% to 10% of wild-type levels) were detected in neutrophils after retroviral-mediated gene transfer, superoxide-generating activity was approximately 20% to 25% of wild-type mouse neutrophils. Expression of gp91(phox) is normally restricted to mature phagocytes. No obvious toxicity was observed in other hematopoietic lineages in transplant recipients, and provirus-marked cells were capable of reconstituting secondary transplant recipients, who also exhibited NADPH oxidase-positive neutrophils. MSCV-based vectors for long-term expression of gp91(phox) may be useful for gene therapy of human CGD targeted at hematopoietic stem cells.
慢性肉芽肿病(CGD)是一种遗传性疾病,其特征为产生超氧化物的吞噬细胞烟酰胺腺嘌呤二核苷酸磷酸(NADPH)氧化酶缺乏,导致反复发生严重的细菌和真菌感染。这种疾病的X连锁形式(X-CGD)是由X连锁基因gp91(phox)(氧化酶黄素细胞色素b558的大亚基)突变引起的。在本研究中,我们使用X-CGD小鼠模型来研究基于小鼠干细胞病毒(MSCV)骨架的逆转录病毒载体表达gp91(phox)的长期功能。将转导的X-CGD骨髓移植到经致死剂量照射的同基因X-CGD小鼠体内后,中性粒细胞和巨噬细胞中的NADPH氧化酶活性可在长达18至24个月的时间内得以重建。Southern印迹分析和二次移植数据显示原病毒整合到多谱系再增殖细胞中。尽管在逆转录病毒介导的基因转移后,中性粒细胞中检测到相对少量的重组gp91(phox)(约为野生型水平的5%至10%),但超氧化物生成活性约为野生型小鼠中性粒细胞的20%至25%。gp91(phox)的表达通常仅限于成熟吞噬细胞。在移植受体的其他造血谱系中未观察到明显毒性,并且原病毒标记的细胞能够重建二次移植受体,这些受体的中性粒细胞也表现出NADPH氧化酶阳性。基于MSCV的载体长期表达gp91(phox)可能对以造血干细胞为靶点的人类CGD基因治疗有用。