Department of Pediatrics and Powell Gene Therapy Center, University of Florida College of Medicine, Gainesville, FL 32610, USA.
Hum Gene Ther. 2011 Aug;22(8):935-49. doi: 10.1089/hum.2010.121. Epub 2011 Mar 13.
Severe combined immune deficiency due to adenosine deaminase (ADA) deficiency is a rare, potentially fatal pediatric disease, which results from mutations within the ADA gene, leading to metabolic abnormalities and ultimately profound immunologic and nonimmunologic defects. In this study, recombinant adeno-associated virus (rAAV) vectors based on serotypes 1 and 9 were used to deliver a secretory version of the human ADA (hADA) gene to various tissues to promote immune reconstitution following enzyme expression in a mouse model of ADA deficiency. Here, we report that a single-stranded rAAV vector, pTR2-CB-Igκ-hADA, (1) facilitated successful gene delivery to multiple tissues, including heart, skeletal muscle, and kidney, (2) promoted ectopic expression of hADA, and (3) allowed enhanced serum-based enzyme activity over time. Moreover, the rAAV-hADA vector packaged in serotype 9 capsid drove partial, prolonged, and progressive immune reconstitution in ADA-deficient mice. Overview Summary Gene therapies for severe combined immune deficiency due to adenosine deaminase (ADA) deficiency (ADA-SCID) over two decades have exclusively involved retroviral vectors targeted to lymphocytes and hematopoietic progenitor cells. These groundbreaking gene therapies represented an unprecedented revolution in clinical medicine but in most cases did not fully correct the immune deficiency and came with the potential risk of insertional mutagenesis. Alternatively, recombinant adeno-associated virus (rAAV) vectors have gained attention as valuable tools for gene transfer, having demonstrated no pathogenicity in humans, minimal immunogenicity, long-term efficacy, ease of administration, and broad tissue tropism (Muzyczka, 1992 ; Flotte et al., 1993 ; Kessler et al., 1996 ; McCown et al., 1996 ; Lipkowitz et al., 1999 ; Marshall, 2001 ; Chen et al., 2003 ; Conlon and Flotte, 2004 ; Griffey et al., 2005 ; Pacak et al., 2006 ; Stone et al., 2008 ; Liu et al., 2009 ; Choi et al., 2010 ). Currently, rAAV vectors are being utilized in phase I/II clinical trials for cystic fibrosis, α-1 antitrypsin deficiency, Canavan's disease, Parkinson's disease, hemophilia, limb-girdle muscular dystrophy, arthritis, Batten's disease, and Leber's congenital amaurosis (Flotte et al., 1996 , 2004 ; Kay et al., 2000 ; Aitken et al., 2001 ; Wagner et al., 2002 ; Manno et al., 2003 ; Snyder and Francis, 2005 ; Maguire et al., 2008 ; Cideciyan et al., 2009 ). In this study, we present preclinical data to support the viability of an rAAV-based gene transfer strategy for cure of ADA-SCID. We report efficient transduction of a variety of postmitotic target tissues in vivo, subsequent human ADA (hADA) expression, and enhanced hADA secretion in tissues and blood, with increasing peripheral lymphocyte populations over time.
腺苷脱氨酶(ADA)缺乏症导致的严重联合免疫缺陷是一种罕见的、潜在致命的儿科疾病,由 ADA 基因内的突变引起,导致代谢异常,最终导致严重的免疫和非免疫缺陷。在这项研究中,基于血清型 1 和 9 的重组腺相关病毒(rAAV)载体被用于将人类 ADA(hADA)基因的分泌型递送至各种组织,以在 ADA 缺乏症小鼠模型中表达酶后促进免疫重建。在这里,我们报告了单链 rAAV 载体 pTR2-CB-Igκ-hADA,(1)能够成功地将基因递送至包括心脏、骨骼肌和肾脏在内的多种组织,(2)促进了 hADA 的异位表达,以及(3)允许随着时间的推移增强基于血清的酶活性。此外,包装在血清型 9 衣壳中的 rAAV-hADA 载体在 ADA 缺陷型小鼠中驱动部分、持续和渐进的免疫重建。
摘要 腺苷脱氨酶(ADA)缺乏症(ADA-SCID)的基因治疗在过去二十年中完全依赖于靶向淋巴细胞和造血祖细胞的逆转录病毒载体。这些开创性的基因治疗在临床医学中代表了前所未有的革命,但在大多数情况下,它们并没有完全纠正免疫缺陷,并且存在插入突变的潜在风险。相反,重组腺相关病毒(rAAV)载体作为基因转移的有价值工具引起了人们的关注,因为它们在人类中没有致病性、最小的免疫原性、长期疗效、易于管理和广泛的组织嗜性(Muzyczka,1992 年;Flotte 等人,1993 年;Kessler 等人,1996 年;McCown 等人,1996 年;Lipkowitz 等人,1999 年;Marshall,2001 年;Chen 等人,2003 年;Conlon 和 Flotte,2004 年;Griffey 等人,2005 年;Pacak 等人,2006 年;Stone 等人,2008 年;Liu 等人,2009 年;Choi 等人,2010 年)。目前,rAAV 载体正在用于囊性纤维化、α-1 抗胰蛋白酶缺乏症、Canavan 病、帕金森病、血友病、肢带型肌营养不良症、关节炎、Batten 病和 Leber 先天性黑蒙的 I/II 期临床试验中(Flotte 等人,1996 年,2004 年;Kay 等人,2000 年;Aitken 等人,2001 年;Wagner 等人,2002 年;Manno 等人,2003 年;Snyder 和 Francis,2005 年;Maguire 等人,2008 年;Cideciyan 等人,2009 年)。在这项研究中,我们提供了临床前数据,支持基于 rAAV 的基因转移策略治疗 ADA-SCID 的可行性。我们报告了在体内有效转导各种有丝分裂后靶组织,随后在组织和血液中表达人 ADA(hADA),并随着时间的推移增加外周淋巴细胞群,增强 hADA 分泌。