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A new strategy to enhance gene therapy for sickle cell diseaseNext, they transduced CD34 + cells obtained from the cord blood of newborns with sickle cell disease. The cells were transduced with a lentiviral vector delivering the gene encoding the anti ...
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Lentiviral vectors offer gene therapy option for hemophilia A patients with anti-AAV antibodiesIn the study, "Lentiviral Gene Therapy with CD34+ Hematopoietic Cells for Hemophilia ... AAV-mediated approaches with the ability to bypass anti-AAV antibodies. There may be some critical ...
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