Interferon-γ inducible factor 16 (IFI16) restricts adeno-associated virus type 2 (AAV2) transduction in an immune-modulatory independent way.
Sereina O SutterKurt ToblerMichael SeyffertAnouk LkharraziJoël ZölligElisabeth M SchranerBernd VogtHildegard BüningCornel FraefelPublished in: Journal of virology (2024)
Adeno-associated virus (AAV) vectors are among the most frequently used viral vectors for gene therapy. The lack of pathogenicity of the parental virus, the long-term persistence as episomes in non-proliferating cells, and the availability of a variety of AAV serotypes differing in their cellular tropism are advantageous features of this biological nanoparticle. To deepen our understanding of virus-host interactions, especially in terms of antiviral responses, we present here the first transcriptome analysis of AAV serotype 2 (AAV2)-infected human primary fibroblasts. Our findings indicate that interferon-γ inducible factor 16 acts as an antiviral factor in AAV2 infection and AAV2 vector-mediated cell transduction in an immune-modulatory independent way by interrupting the Sp1-dependent gene expression from viral or vector genomes.
Keyphrases
- gene therapy
- gene expression
- single cell
- endothelial cells
- dendritic cells
- induced apoptosis
- stem cells
- rna seq
- bone marrow
- cell proliferation
- zika virus
- genome wide
- cystic fibrosis
- cell death
- klebsiella pneumoniae
- endoplasmic reticulum stress
- dengue virus
- pseudomonas aeruginosa
- induced pluripotent stem cells
- cell cycle arrest
- biofilm formation
- aedes aegypti