Kremer E J, Perricaudet M
Laboratoire de Génétique de Virus Oncogènes, Institut Gustave Roussy, Villejuif, France.
Br Med Bull. 1995 Jan;51(1):31-44. doi: 10.1093/oxfordjournals.bmb.a072951.
In this review we describe current strategies for adenoviral mediated gene transfer (AMGT) and adeno-associated viral mediated gene transfer (AAVMGT). We consider the structure and molecular biology of adenoviruses and adeno-associated viruses and detail the current advantages and disadvantages of AMGT and AAVMGT. Potential solutions to some of the specific drawbacks to AMGT, including the development of new vectors, addition of gp19k, organoides, and the use of non-human adenoviral vectors, are discussed.
在本综述中,我们描述了腺病毒介导的基因转移(AMGT)和腺相关病毒介导的基因转移(AAVMGT)的当前策略。我们考虑了腺病毒和腺相关病毒的结构与分子生物学,并详细阐述了AMGT和AAVMGT目前的优缺点。还讨论了针对AMGT某些特定缺点的潜在解决方案,包括新型载体的开发、添加gp19k、类器官以及使用非人类腺病毒载体。