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Advisory BoardThe following people have generously agreed to be on the Stop ALD Foundation's Advisory Board: Click on the names below for more
information...
Dr. Aubourg's clinical specialty is neurology
and pediatrics. He is the team director at the Research Unit INSERM
U342. As well, he is the Director of the Ph.D. program. His research
interests include gene therapy and genetics of neurodegenerative diseases
including adrenoleukodystrophy (ALD). His main publications include Nature
(1), New England Journal of Mediine (2), Lancet (1), Trends in
Neuroscience (1), PNAS, (1), Human Gene Therapy, and the Journal
of Biological Chemistry.
At the University of Pennsylvania, Dr. Wilson's research focuses on the understanding of basic pathogenesis of human inherited diseases in the development of novel therapies based on somatic gene transfer. One disease model under investigation in his laboratory is cystic fibrosis. Previous work involves characterization of CF gene expression in the human lung, the development of an animal model for CF, and creation of recombinant viruses for lung-directed gene therapy. Current efforts attempt to understand the biology of airway epithelium with respect to development, lineage relationships and stem cells, biogenesis of normal and mutant CFTR, and submucosal gland morphogenesis and function. His attempts to understand the basis for bacterial infection in the CF lung has lead to the discovery of a number of new molecules called human defensins. These are antibiotic peptides secreted by epithelial cells and constitute an important part of innate immunity. A particular interest to the effort in gene therapy for cystic fibrosis is the immunology of in vivo administration of recombinant viruses. Dr. Wilson's laboratory studies specifically the basic cellular and molecular biology of host response to a recombinant virus with the goal of delineating mechanisms of antigen-specific immunity, as well as developing strategies to overcome these potential barriers. Critical to the success of effective in vivo
therapies is the development of viral based vectors. Dr. Wilson's laboratory has
taken a broad-based approach to vector development utilizing both DNA and RNA
viruses. Substantial efforts have been placed in the study of vectors based on
human adenoviruses. Included in this work is the interaction of the vector with
the host with respect to antigen and nonantigen specific immune mediated
processes. A new area of pursuit is the use of vectors based on lentiviruses.
These RNA viruses are capable of transduction in non-diving cells. Initial work
is focused on vectors based on HIV, although future studies are moving towards
lentiviruses isolated from other species.
As president of the Global Health Program at the Bill & Melinda Gates Foundation, Dr. Tadataka (Tachi) Yamada leads the foundation’s efforts to help develop and deliver low-cost, life-saving health tools for the developing world. Before joining the foundation, Yamada served as Chairman
of Research and Development and was a member of the Board of Directors at
GlaxoSmithKline. Prior to that, he was chairman of the Department of Internal
Medicine at the University of Michigan Medical School and Physician-in-Chief at
the University of Michigan Medical Center. Yamada is a past president of the
American Gastroenterological Association and the Association of American
Physicians, a master of the American College of Physicians, and a member of the
Institute of Medicine of the National Academy of Science in the United States
and the Academy of Medical Sciences in the United Kingdom.
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