Literature DB >> 15006600

Role of viral vectors and virion shells in cellular gene expression.

Jackie L Stilwell1, Richard Jude Samulski.   

Abstract

The role of the virion shell in viral pathogenesis is relatively unknown yet the use of viral vectors in human gene transfer experiments requires an understanding of these interactions. In this study, we used DNA microarrays to identify genes modulated during pathogenic adenovirus or nonpathogenic adeno-associated virus infections. Responses to wt viruses, recombinant vectors, or empty virion particles were compared. Adeno-associated virus shells induced nearly the full complement of changes elicited by the intact virus. The cellular genes elicited a nonpathogenic response, with antiproliferative genes being induced as a cluster. In contrast, adenovirus and adenovirus empty capsid infection yielded a broader response and subset, respectively, including induction of immune and stress-response genes associated with pathogenic effects. Our studies show that the impact of the viral capsid on cellular gene expression, and potential host toxicity, must be considered independent of the vector genome for safe gene transfer in the clinic.

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Year:  2004        PMID: 15006600     DOI: 10.1016/j.ymthe.2003.11.007

Source DB:  PubMed          Journal:  Mol Ther        ISSN: 1525-0016            Impact factor:   11.454


  23 in total

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Review 4.  Innate immune recognition of viruses and viral vectors.

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Journal:  J Virol       Date:  2008-05-14       Impact factor: 5.103

6.  Self-complementary AAV virus (scAAV) safe and long-term gene transfer in the trabecular meshwork of living rats and monkeys.

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8.  Large-scale analysis of adeno-associated virus vector integration sites in normal human cells.

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Journal:  J Virol       Date:  2005-09       Impact factor: 5.103

9.  Comparative Evaluation of the Vaccine Efficacies of Three Adenovirus-Based Vector Types in the Friend Retrovirus Infection Model.

Authors:  Camilla Patrizia Hrycak; Sonja Windmann; Wibke Bayer
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10.  Induction of immune tolerance to FIX by intramuscular AAV gene transfer is independent of the activation status of dendritic cells.

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Journal:  Blood       Date:  2009-11-17       Impact factor: 22.113

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