Evaluation of Genetic Markers as Explanations for the Observed Differences in Disease Progression in HIV+ Youth
Status: | Completed |
---|---|
Conditions: | HIV / AIDS |
Therapuetic Areas: | Immunology / Infectious Diseases |
Healthy: | No |
Age Range: | Any |
Updated: | 3/1/2017 |
Start Date: | December 2002 |
End Date: | September 2005 |
Evaluation of HIV-Specific CD8+ T-Cell Responses and Escape Mutations as Explanations for the Observed Differences in Disease Progression Conferred by HLA Class I Alleles
This protocol is a study of HIV+ young people who were identified as having certain HIV-1
specific T-cell responses and genetic markers while previously enrolled in the 5-year
longitudinal adolescent study, "REACH." Blood samples will be collected, a medical and
medication history and physical examination will be performed every 6 months for a total of
2 years.
specific T-cell responses and genetic markers while previously enrolled in the 5-year
longitudinal adolescent study, "REACH." Blood samples will be collected, a medical and
medication history and physical examination will be performed every 6 months for a total of
2 years.
Numerous studies have demonstrated an association between HLA class I genotypes with
differing progression to AIDS in individuals who are followed after being off antiretroviral
therapy. These studies do not always associate the same HLA class I alleles with the risks
of HIV-1 disease progression; however they consistently demonstrated that HLA-B*35 and B*53
portend a bad outcome compared to the better outcome observed in HLA-B*27 and B*57 carriers.
Despite this information, very little data exists to explain the mechanism of this
association.
This longitudinal study will look at the HIV-1 specific CD8+ T-cell responses and the
dominant HIV-1 genotype among individuals identified as HLA-B*27, B*35, B*53 and B*57
positive through studies done in collaboration with the REACH project.
differing progression to AIDS in individuals who are followed after being off antiretroviral
therapy. These studies do not always associate the same HLA class I alleles with the risks
of HIV-1 disease progression; however they consistently demonstrated that HLA-B*35 and B*53
portend a bad outcome compared to the better outcome observed in HLA-B*27 and B*57 carriers.
Despite this information, very little data exists to explain the mechanism of this
association.
This longitudinal study will look at the HIV-1 specific CD8+ T-cell responses and the
dominant HIV-1 genotype among individuals identified as HLA-B*27, B*35, B*53 and B*57
positive through studies done in collaboration with the REACH project.
Inclusion Criteria:
- HLA-Class I HLA-B*27, B*35, B*53 and/or B*57 positive identified through the REACH
study
- Subject's ability and willingness to provide written informed consent
- Subject's ability and willingness to be followed at least one year on this ATN 026
study
Exclusion Criteria:
- On chronic immunosuppressive therapy, not including topical or inhaled steroid use.
- Any prohibited medication listed in protocol within 2 weeks prior to the Entry visit
labs
We found this trial at
10
sites
Mount Sinai Med Ctr Founded in 1852, The Mount Sinai Hospital is a 1,171-bed, tertiary-care...
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Childrens Hospital Los Angeles Children's Hospital Los Angeles is a 501(c)(3) nonprofit hospital for pediatric...
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Children's Hospital of Philadelphia Since its start in 1855 as the nation's first hospital devoted...
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University of Maryland As a globally-connected university offering a world-class education, the University of Maryland...
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111 Michigan Ave NW
Washington, District of Columbia
Washington, District of Columbia
(202) 476-5000
Childrens National Medical Center As the nation’s children’s hospital, the mission of Children’s National Medical...
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