Adenovirus vectors deleted for genes essential for viral DNA replication
- PMID: 15769613
- DOI: 10.2741/1607
Adenovirus vectors deleted for genes essential for viral DNA replication
Abstract
Adenovirus (Ad) gene therapy vectors made replication defective by deletion of the E1 region (first-generation vectors) induce high-level inflammation that leads to loss of both transduced gene expression and transduced cells. First-generation vectors were initially considered to be incapable of viral DNA replication, but it is necessary to delete one or more of the genes, all in the E2 transcription unit, that encode proteins essential for Ad DNA replication to completely eliminate viral DNA replication. Vectors deleted for one or more of the E2 genes (second-generation vectors) induce reduced levels of inflammation in certain animal models and offer promise for understanding the mechanisms by which adenovirus vectors induce inflammation and how inflammation can be inhibited. While first-generation vectors dominated the initial human gene therapy trials using adenovirus vectors, second-generation vectors may offer greater promise and greater safety for clinical studies.
Similar articles
-
An adenovirus type 5 (Ad5) amplicon-based packaging cell line for production of high-capacity helper-independent deltaE1-E2-E3-E4 Ad5 vectors.J Virol. 2005 May;79(10):6400-9. doi: 10.1128/JVI.79.10.6400-6409.2005. J Virol. 2005. PMID: 15858023 Free PMC article.
-
Production and characterization of improved adenovirus vectors with the E1, E2b, and E3 genes deleted.J Virol. 1998 Feb;72(2):926-33. doi: 10.1128/JVI.72.2.926-933.1998. J Virol. 1998. PMID: 9444984 Free PMC article.
-
Conditional repression of the E2 transcription unit in E1-E3-deleted adenovirus vectors is correlated with a strong reduction in viral DNA replication and late gene expression in vitro.J Virol. 1997 Apr;71(4):3307-11. doi: 10.1128/JVI.71.4.3307-3311.1997. J Virol. 1997. PMID: 9060700 Free PMC article.
-
Adenovirus vectors for gene therapy, vaccination and cancer gene therapy.Curr Gene Ther. 2013 Dec;13(6):421-33. doi: 10.2174/1566523213666131125095046. Curr Gene Ther. 2013. PMID: 24279313 Free PMC article. Review.
-
[Development of a novel adenovirus vector exhibiting microRNA-mediated suppression of the leaky expression of adenovirus genes].Yakugaku Zasshi. 2012;132(12):1407-12. doi: 10.1248/yakushi.12-00235-5. Yakugaku Zasshi. 2012. PMID: 23208048 Review. Japanese.
Cited by
-
Role of Adenoviruses in Cancer Therapy.Front Oncol. 2022 Jun 9;12:772659. doi: 10.3389/fonc.2022.772659. eCollection 2022. Front Oncol. 2022. PMID: 35756634 Free PMC article. Review.
-
Replication of type 5 adenovirus promotes middle ear infection by Streptococcus pneumoniae in the chinchilla model of otitis media.Pathog Dis. 2015 Mar;73(2):1-8. doi: 10.1111/2049-632X.12216. Epub 2015 Feb 26. Pathog Dis. 2015. PMID: 25251686 Free PMC article.
-
Vaccines based on the replication-deficient simian adenoviral vector ChAdOx1: Standardized template with key considerations for a risk/benefit assessment.Vaccine. 2022 Aug 19;40(35):5248-5262. doi: 10.1016/j.vaccine.2022.06.008. Epub 2022 Jun 14. Vaccine. 2022. PMID: 35715352 Free PMC article.
-
E1B and E4 oncoproteins of adenovirus antagonize the effect of apoptosis inducing factor.Virology. 2014 May;456-457:205-19. doi: 10.1016/j.virol.2014.03.010. Epub 2014 Apr 15. Virology. 2014. PMID: 24889240 Free PMC article.
-
Targeted DNA Demethylation: Vectors, Effectors and Perspectives.Biomedicines. 2023 Apr 30;11(5):1334. doi: 10.3390/biomedicines11051334. Biomedicines. 2023. PMID: 37239005 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Other Literature Sources