Gene therapy for hemophilia; adeno-associated viral (AAV) vectors; immune tolerance induction to therapeutic proteins; immune response and tolerance mechanisms (including viral immunology, oral tolerance, regulatory T cells)

His research interests are in gene therapy and immune tolerance for hemophilia and in AAV vectors

Subject Areas:

  • Gene and Cell Therapy
PhD, Auburn University, Microbiology, 1996
BS, University of Kaiserslautern, Biology, 1992