AAV-Mediated Gene Therapy for Research and Therapeutic Purposes
- PMID: 26958729
- DOI: 10.1146/annurev-virology-031413-085355
AAV-Mediated Gene Therapy for Research and Therapeutic Purposes
Abstract
Adeno-associated virus (AAV) is a small, nonenveloped virus that was adapted 30 years ago for use as a gene transfer vehicle. It is capable of transducing a wide range of species and tissues in vivo with no evidence of toxicity, and it generates relatively mild innate and adaptive immune responses. We review the basic biology of AAV, the history of progress in AAV vector technology, and some of the clinical and research applications where AAV has shown success.
Keywords: DNA transfer; gene therapy; parvovirus; transduction; viral vector.
Similar articles
-
Gene therapy methods in bone and joint disorders. Evaluation of the adeno-associated virus vector in experimental models of articular cartilage disorders, periprosthetic osteolysis and bone healing.Acta Orthop Suppl. 2007 Apr;78(325):1-64. Acta Orthop Suppl. 2007. PMID: 17427340 Review.
-
Adeno-associated virus vectors for gene therapy of neurodegenerative disorders.Clin Neurosci. 1995-1996;3(5):292-300. Clin Neurosci. 1995. PMID: 8914796 Review.
-
Progress in the use of adeno-associated viral vectors for gene therapy.Cells Tissues Organs. 2004;177(3):139-50. doi: 10.1159/000079988. Cells Tissues Organs. 2004. PMID: 15388988 Review.
-
Immunity to adeno-associated virus vectors in animals and humans: a continued challenge.Gene Ther. 2008 Jun;15(11):808-16. doi: 10.1038/gt.2008.54. Epub 2008 Apr 3. Gene Ther. 2008. PMID: 18385765 Review.
-
Recent developments in adeno-associated virus vector technology.J Gene Med. 2008 Jul;10(7):717-33. doi: 10.1002/jgm.1205. J Gene Med. 2008. PMID: 18452237 Review.
Cited by
-
The longitudinal kinetics of AAV5 vector integration profiles and evaluation of clonal expansion in mice.Mol Ther Methods Clin Dev. 2024 Jun 26;32(3):101294. doi: 10.1016/j.omtm.2024.101294. eCollection 2024 Sep 12. Mol Ther Methods Clin Dev. 2024. PMID: 39104575 Free PMC article.
-
The power and the promise of CRISPR/Cas9 genome editing for clinical application with gene therapy.J Adv Res. 2022 Sep;40:135-152. doi: 10.1016/j.jare.2021.11.018. Epub 2021 Dec 4. J Adv Res. 2022. PMID: 36100322 Free PMC article. Review.
-
Identification and Functional Analysis of Novel Nonstructural Proteins of Human Bocavirus 1.J Virol. 2015 Oct;89(19):10097-109. doi: 10.1128/JVI.01374-15. Epub 2015 Jul 29. J Virol. 2015. PMID: 26223640 Free PMC article.
-
Transcriptional repression of PTEN in neural cells using CRISPR/dCas9 epigenetic editing.Sci Rep. 2020 Jul 9;10(1):11393. doi: 10.1038/s41598-020-68257-y. Sci Rep. 2020. PMID: 32647121 Free PMC article.
-
Anti-AAV Antibodies in AAV Gene Therapy: Current Challenges and Possible Solutions.Front Immunol. 2021 Mar 17;12:658399. doi: 10.3389/fimmu.2021.658399. eCollection 2021. Front Immunol. 2021. PMID: 33815421 Free PMC article. Review.
LinkOut - more resources
Full Text Sources
Other Literature Sources