Dexamethasone administration at a late time point could enhance transgene expression

Dexamethasone, a glucocorticoid with anti-inflammatory and immunosuppressive effects, can transiently increase the expression of therapeutic genes delivered using adeno-associated virus (AAV) vectors. A new study, which showed that dexamethasone administration at a late time point could increase transgene expression from AAV9 vector transduced liver in mice, was published in the peer-reviewed journal Human Gene Therapy.

Corticosteroids like dexamethasone, methylprednisolone and prednisone are frequently used in AAV-based human gene therapy protocols, but the optimal timing of such therapy has not been thoroughly studied. This paper provides an interesting insight into the potential effects of short-duration steroid therapy."

Terence R. Flotte, MD, Editor-in-Chief of Human Gene Therapy

Chengwen Li, PhD and coauthors from the University of North Carolina at Chapel Hill demonstrated that the increased transgene expression was not dependent on the duration or time point of dexamethasone administration after AAV injection. The researchers did not report increased transgene expression in hemophilia dogs treated with dexamethasone after AAV gene therapy.

"These results provided valuable information to design an effective approach for application of dexamethasone in future clinical studies with AAV vector liver targeted gene therapy, such as short term and intermittent administration of steroids," state the investigators. "This may decrease the toxicities from long term application of steroids and also avoid liver damage from high doses of AAV vector seen in clinical trials."


Mary Ann Liebert, Inc.

Journal reference:

Zheng Chai, Xintao Zhang, Amanda Lee Dobbins, Richard Jude Samulski, Elizabeth P. Merricks, Timothy C. Nichols, and Chengwen Li. Human Gene Therapy.

Posted in: Genomics

Tags: Anti-Inflammatory, Dexamethasone, Gene, Gene Therapy, Genes, Glucocorticoid, Hemophilia, Liver, Prednisone, Steroid, Transgene, Virus

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