Regulated hAAT Expression from a Novel rAAV Vector and Its Application in the Prevention of Type 1 Diabetes
Autor: | Clive Wasserfall, Yuanqing Lu, Lonneke van der Meijden-Erkelens, Mark A. Atkinson, Sihong Song, Hongxia Ma, Keith Lowe |
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Jazyk: | angličtina |
Rok vydání: | 2019 |
Předmět: |
Genetic enhancement
Transgene lcsh:Medicine autoimmune disease Nod type 1 diabetes (T1D) Article Viral vector Gene product 03 medical and health sciences 0302 clinical medicine recombinant adeno-associated virus (rAAV) Gene silencing Medicine Vector (molecular biology) 030304 developmental biology Doxycycline 0303 health sciences business.industry tet-on promoter lcsh:R General Medicine gene therapy 3. Good health serine proteinase inhibitor (SERPIN) Cancer research alpha 1 antitrypsin (AAT) business 030217 neurology & neurosurgery medicine.drug |
Zdroj: | Journal of Clinical Medicine Volume 8 Issue 9 Journal of Clinical Medicine, Vol 8, Iss 9, p 1321 (2019) |
ISSN: | 2077-0383 |
DOI: | 10.3390/jcm8091321 |
Popis: | We, and others, have previously achieved high and sustained levels of transgene expression from viral vectors, such as recombinant adeno-associated virus (rAAV). However, regulatable transgene expression may be preferred in gene therapy for diseases, such as type 1 diabetes (T1D) and rheumatoid arthritis (RA), in which the timing and dosing of the therapeutic gene product play critical roles. In the present study, we generated a positive feedback regulation system for human alpha 1 antitrypsin (hAAT) expression in the rAAV vector. We performed quantitative kinetics studies in vitro and in vivo demonstrating that this vector system can mediate high levels of inducible transgene expression. Transgene induction could be tailored to occur rapidly or gradually, depending on the dose of the inducing drug, doxycycline (Dox). Conversely, after withdrawal of Dox, the silencing of transgene expression occurred slowly over the course of several weeks. Importantly, rAAV delivery of inducible hAAT significantly prevented T1D development in non-obese diabetic (NOD) mice. These results indicate that this Dox-inducible vector system may facilitate the fine-tuning of transgene expression, particularly for hAAT treatment of human autoimmune diseases, including T1D. |
Databáze: | OpenAIRE |
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