Human leukocyte antigen genotype and risk of HIV disease progression before and after initiation of antiretroviral therapy
- PMID: 21849458
- PMCID: PMC3187522
- DOI: 10.1128/JVI.00804-11
Human leukocyte antigen genotype and risk of HIV disease progression before and after initiation of antiretroviral therapy
Abstract
While the human leukocyte antigen (HLA) genotype has been associated with the rate of HIV disease progression in untreated patients, little is known regarding these relationships in patients using highly active antiretroviral therapy (HAART). The limited data reported to date identified few HLA-HIV disease associations in patients using HAART and even occasional associations that were opposite of those found in untreated patients. We conducted high-resolution HLA class I and II genotyping in a random sample (n = 860) of HIV-seropositive women enrolled in a long-term cohort initiated in 1994. HLA-HIV disease associations before and after initiation of HAART were examined using multivariate analyses. In untreated HIV-seropositive patients, we observed many of the predicted associations, consistent with prior studies. For example, HLA-B*57 (β = -0.7; 95% confidence interval [CI] = -0.9 to -0.5; P = 5 × 10⁻¹¹) and Bw4 (β = -0.2; 95% CI = -0.4 to -0.1; P = 0.009) were inversely associated with baseline HIV viral load, and B*57 was associated with a low risk of rapid CD4+ decline (odds ratio [OR] = 0.2; 95% CI = 0.1 to 0.6; P = 0.002). Conversely, in treated patients, the odds of a virological response to HAART were lower for B*57:01 (OR = 0.2; 95% CI = 0.0 to 0.9; P = 0.03), and Bw4 (OR = 0.4; 95% CI = 0.1 to 1.0; P = 0.04) was associated with low odds of an immunological response. The associations of HLA genotype with HIV disease are different and sometimes even opposite in treated and untreated patients.
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References
-
- Ahdieh L., et al. 2000. Selection by indication of potent antiretroviral therapy use in a large cohort of women infected with human immunodeficiency virus. Am. J. Epidemiol. 152:923–933 - PubMed
-
- Anonymous 1992. 1993 revised classification system for HIV infection and expanded surveillance case definition for AIDS among adolescents and adults. MMWR Recommend. Rep. 41(RR-17): 1–19 - PubMed
-
- Barkan S. E., et al. 1998. The Women's Interagency HIV Study. WIHS Collaborative Study Group. Epidemiology 9:117–125 - PubMed
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