期刊文献+

腺相关病毒的研究进展与展望 被引量:1

Research Progress on Adeno-associated Virus
下载PDF
导出
摘要 腺相关病毒是动物病毒中最小,基因结构最简单的一类单链DNA缺陷病毒。其最早于1965年作为腺病毒制备物中的一种污染成分被发现。在培养的正常细胞中,单纯的腺相关病毒并不发生毒性感染,只有在与其他辅助病毒发生共同感染时才能产生作用。由于安全性好、宿主范围广、免疫原性低等特点,腺相关病毒被广泛应用于基因表达载体的构建及基因治疗。腺相关病毒的随机整合性仍然可能引起临床应用上的潜在危险。在阐述该病毒的分子结构及其在生物学上的特点基础上,说明其在实际生产中的运用,并对其有关研究进行了展望。 Adeno-associated virus (AAV) is the smallest defective animal virus with a simple gene structure and a single stranded DNA. As early as 1965, AAV had been found as a kind of pollution components in the adenovirus preparation. AAV can’t infect normal cells alone in culture, and can only have a common infection with other helper virus. AAV has been widely used in the construction of gene expression and gene therapy for its safety, board host and low immunogenicity. Random integration of AAV may cause a potential risk for clinical application. In the view, we will elaborate the molecular structure and biological characteristics of the virus. At the same time, we will also illustrate its application in production.
作者 黄灿 陈珍
出处 《生物灾害科学》 2014年第4期333-336,共4页 Biological Disaster Science
基金 国家自然科学基金资助项目(30970880)
关键词 腺相关病毒 随机整合 分子结构 基因治疗 安全性 AAV random integration molecular structure gene therapy safety
  • 相关文献

参考文献4

二级参考文献73

  • 1郑文岭,马文丽.消化道基因治疗:中医药治疗机制的探讨[J].科技导报,1994,12(12):8-11. 被引量:18
  • 2阎钟钰,丛敏,王萍,唐淑珍,王宝恩,贾继东,刘勇,尤红.腺相关病毒Rep78蛋白对乙型肝炎病毒C基因的抑制作用[J].中华肝脏病杂志,2005,13(3):187-189. 被引量:3
  • 3刘天会,丛敏,王萍,唐淑珍,刘晓明,王宝恩,贾继东,尤红.腺相关病毒Rep78蛋白抑制乙型肝炎病毒复制的体外研究[J].肝脏,2006,11(6):396-398. 被引量:3
  • 4Brining H. Gene therapy enters the pharma market: the short story of a long journey[J]. EMBO Molecular Medicine, 2013, 5(1): 1-3. 被引量:1
  • 5Maguire AM, Simonelli F, Pierce EA, et al. Safety and efficacy of gene transfer for Leber's congenital amaurosis[J]. The New England Journal Medicine, 2008, 358(21): 2240-2248. 被引量:1
  • 6Manno CS, Pierce GF, Arruda VR, et al. Successful transduction of liver in hemophilia by AAV-factor IX and limitations imposed by the host immune response[J].Nature Medicine, 2006, 12(3): 342-592. 被引量:1
  • 7Mingozzi F, Meulenberg J J, Hui D J, et al. AAV-l-mediated gene transfer to skeletal muscle in humans results in dose-dependent activation of capsid-specific T cells[J]. Blood, 2009, 14(10): 2077-2086. 被引量:1
  • 8Flotte TR, Trapnell BC, Humphries M, et al. Phase 2 clinical trial of a recombinant adeno-ass0ciated virus vector expressing alpha 1 antitrypsin: Interim results[J]. Human Gene Therapy, 2011, 22(10): 1239-1247. 被引量:1
  • 9Allay JA, Sleep SE, Long S, et al. Good manufacturing practice production of self-complementary serotype 8 adeno-associated viral vector for a hemophilia B clinical trial[J]. Human Gene Therapy, 2011, 22(5): 595-604. 被引量:1
  • 10Marks WJ Jr, Bartus RT, Siffert J, et al. Gene delivery of AAV2-neurturin for Parkinson's disease: a double-blind, randomised, controlled trial[J]. The Lancet Neurology, 2010, 9(12): 1164-1172. 被引量:1

共引文献8

同被引文献6

引证文献1

二级引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部