Immune responses to AAV vectors: overcoming barriers to successful gene therapy.
By F. Mingozzi, K. High. Blood, 2013
901 citations recorded by the source corpus.
Subfields: Genetics, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/b3211ffcff16d05857cb216feab6a7d7596a7abb
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In Genetics
In Molecular Biology
Citations in the corpus
- Challenges and advances in clinical applications of mesenchymal stromal cells (2021, background): “The adverse immune reactions induced by viral transduction were reported to impair the stability of transgenes [126, 127].”
- Gene therapy comes of age (2018, positive): “Problems that still need to be addressed include the delayed CD8 T cell response to the capsid, which has been well controlled with a short course of steroids with some AAV vectors but not with others, and the prevalence—particularly in the adult population— of preexisting neutralizing antibodies to”
- Current Strategies for Brain Drug Delivery (2018, background): “So far, AVV vectors have demonstrated exceptional safety profiles in humans as well as the ability for gene delivery in the brain, although a concern on immunogenicity still remains [21].”