AIDS Clinical Trial
Official title:
Comparison of HIV-1 Epitopes That May be Recognized by HLA-B*3501 (PY) and -B*3503 (Px) Early After Seroconversion and After Development of AIDS
This study will identify variations in the genome of the human immunodeficiency virus (HIV)
early after infection and following the development of AIDS. It will analyze genetic
material and clinical data from HIV-positive individuals to assess differences in viral
epitopes between patients with two different gene alleles (alternative forms of a
gene)-B*3501 and B*3503. (An epitope is a molecular region on the surface of an antigen
capable of eliciting an immune response and of combining with the specific antibody produced
by such a response.)
HIV disease in people with the B*3503 allele progresses significantly faster than it does in
people with the B*3501 allele. This study might provide information that is potentially
useful in developing a successful HIV vaccine.
Blood samples and clinical data for analysis will be obtained from the Johns Hopkins
Bloomberg School of Public Health; the University of Pittsburgh; the John H. Stroger, Jr.
Hospital of Cook County; the Howard Brown Health Center; Northwestern University; and the
University of California at Los Angeles.
The purpose of this study is to identify variations in the genome of HIV early after infection and following the development of AIDS to determine the location of escape mutations that might provide information about potential B*35 epitopes. These data will be useful in explaining the difference in disease progression between individuals possessing B*35 Px alleles and those with B*35 PY alleles. We have previously shown that individuals with B*35 Px alleles progress at a significantly faster rate compared to those with B*35 PY alleles. This study might provide information which is potentially useful in the development of a successful HIV vaccine. ;
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