We are using cDNA microarrys to assess gene expression changes in a varitey of disorders with a viral pathogenesis. This includes work intended to exaime gene therapy vectors for AIDs and other disorders. Very little is known about how cellular gene expression is affected by the transduction process or transgene expression. Studying the global changes in gene expression of cells transduced with different viral vectors is necessary for understanding the biology of gene therapy, and should yield safer, more effectivetherapies for disorders including AIDs. These studies will help to address potential safety concerns as well as provide information to be used as a basis for designing better vectors. Studies are also focused on the Ebola viruses whhich are filamentous, enveloped, nonsegmented RNA viruses. Although most Ebola viruses, notably Ebola-Zaire virus, are highly infectious for primates and can cause severe haemorrhagic diseases, Ebola-Reston virus does not cause serious disease in humans. Microarray technology is being employed to compare cellular gene responses to Ebola-Zaire and Ebola- Reston virus infection of primary human monocytes, the early targets of Ebola-Zaire virus infection. The study seeks to determine the possible influence of differences in cellular gene expression observed between Ebola-Zaire and Ebola-Reston viruses on the ability of these viruses to cause diseases. - AIDs, microarray, Ebola-Reston, Ebola-Zaire, gene therapy - Neither Human Subjects nor Human Tissues

Agency
National Institute of Health (NIH)
Institute
National Human Genome Research Institute (NHGRI)
Type
Intramural Research (Z01)
Project #
1Z01HG000147-01
Application #
6227987
Study Section
Special Emphasis Panel (CGB)
Project Start
Project End
Budget Start
Budget End
Support Year
1
Fiscal Year
1999
Total Cost
Indirect Cost
Name
National Human Genome Research Institute
Department
Type
DUNS #
City
State
Country
United States
Zip Code