Haut Larissa H, Gill Amanda L, Kurupati Raj K, Bian Ang, Li Yan, Giles-Davis Wynetta, Xiang Zhiquan, Zhou Xiang Yang, Ertl Hildegund C J
1 The Wistar Institute , Philadelphia, Pennsylvania.
2 Current address: Clinical Molecular Regulation Section/Laboratory of Immunoregulation, National Institute of Allergy and Infectious Diseases, National Institutes of Health , Bethesda, Maryland.
Hum Gene Ther Methods. 2016 Oct;27(5):187-196. doi: 10.1089/hgtb.2016.044. Epub 2016 Sep 7.
Adenovirus (Ad) is used extensively for construction of viral vectors, most commonly with deletion in its E1 and/or E3 genomic regions. Previously, our attempts to insert envelope proteins (Env) of HIV-1 into such vectors based on chimpanzee-derived Ad (AdC) viruses were thwarted. Here, we describe that genetic instability of an E1- and E3-deleted AdC vector of serotype C6 expressing Env of HIV-1 can be overcome by reinsertion of E3 sequences with anti-apoptotic activities. This partial E3 deletion presumably delays premature death of HEK-293 packaging cell lines due to Env-induced cell apoptosis. The same partial E3 deletion also allows for the generation of stable glycoprotein 140 (gp140)- and gp160-expressing Ad vectors based on AdC7, a distinct AdC serotype. Env-expressing AdC vectors containing the partial E3 deletion are genetically stable upon serial cell culture passaging, produce yields comparable to those of other AdC vectors, and induce transgene product-specific antibody responses in mice. A partial E3 deletion thereby allows expansion of the repertoire of transgenes that can be expressed by Ad vectors.
腺病毒(Ad)被广泛用于构建病毒载体,最常见的是在其E1和/或E3基因组区域进行缺失。此前,我们尝试将HIV-1的包膜蛋白(Env)插入基于黑猩猩来源的Ad(AdC)病毒的此类载体中,但受阻。在此,我们描述了通过重新插入具有抗凋亡活性的E3序列,可以克服表达HIV-1 Env的C6型E1和E3缺失AdC载体的遗传不稳定性。这种部分E3缺失可能会延迟HEK-293包装细胞系因Env诱导的细胞凋亡而过早死亡。相同的部分E3缺失也允许基于不同的AdC血清型AdC7产生稳定表达糖蛋白140(gp140)和gp160的Ad载体。含有部分E3缺失的表达Env的AdC载体在连续细胞培养传代后遗传稳定,产生的产量与其他AdC载体相当,并在小鼠中诱导转基因产物特异性抗体反应。因此,部分E3缺失允许扩展可由Ad载体表达的转基因库。