| Literature DB >> 27604324 |
Larissa H Haut1, Amanda L Gill1,2, Raj K Kurupati1, Ang Bian1, Yan Li1, Wynetta Giles-Davis1, Zhiquan Xiang1, Xiang Yang Zhou1, Hildegund C J Ertl1.
Abstract
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.Entities:
Keywords: HIV-1; genetic stability; immune responses; vaccine
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Year: 2016 PMID: 27604324 PMCID: PMC5069709 DOI: 10.1089/hgtb.2016.044
Source DB: PubMed Journal: Hum Gene Ther Methods ISSN: 1946-6536 Impact factor: 2.396