Nikolas I Wada, Yue Chen, Arlene Bullotta, Natalie Suder-Egnot, Chengli Shen, Amber D'Souza, Marta Epeldegui, Jay H Bream, Eun-Young Kim, Charles R Rinaldo
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引用次数: 0
Abstract
In men with (MWH) and without (MWOH) HIV-1 infection, we longitudinally evaluated the prevalence of human herpesvirus (HHV) and GB virus C (GBV-C) infections and examined associations with plasma HIV-1 load and inflammatory markers. We analyzed 11,874 plasma samples (collected from 1984 to 2009) from 1,882 men who have sex with men in the Multicenter AIDS Cohort Study to quantify four HHVs [cytomegalovirus (CMV), Epstein-Barr virus (EBV), human herpesvirus 8 (HHV-8), and human herpesvirus 6 (HHV-6)] and GBV-C. HHV and GBV-C viral loads were measured using quantitative Polymerase Chain Reaction (PCR) and Reverse Transcription (RT)-PCR, respectively. Differences in viral prevalence and concentrations were assessed using multivariable logistic and linear regression. Associations between HHV viremia and 24 inflammatory and immune activation biomarkers were evaluated using generalized gamma models. Age-related biomarker trajectories were analyzed using linear mixed models among MWH with sustained suppression due to HIV-1 antiretroviral therapy. MWH with detectable plasma HIV-1 RNA had significantly higher odds of CMV, EBV, and HHV-8 viremia compared with those with undetectable plasma HIV-1 RNA, who in turn had higher odds than MWOH. CMV and EBV viremia were associated with higher levels of multiple inflammatory markers. Among MWH with consistent viral suppression, no significant differences were observed in age-related biomarker trajectories. Overall, active HHV infection, as indicated by viremia, was associated with significantly higher plasma HIV-1 loads and increased inflammatory marker levels-particularly in the presence of detectable plasma HIV-1 RNA. Our study supports the hypothesis that active HHV infections may exacerbate HIV-1 disease progression in MWH.
期刊介绍:
AIDS Research and Human Retroviruses was the very first AIDS publication in the field over 30 years ago, and today it is still the critical resource advancing research in retroviruses, including AIDS. The Journal provides the broadest coverage from molecular biology to clinical studies and outcomes research, focusing on developments in prevention science, novel therapeutics, and immune-restorative approaches. Cutting-edge papers on the latest progress and research advances through clinical trials and examination of targeted antiretroviral agents lead to improvements in translational medicine for optimal treatment outcomes.
AIDS Research and Human Retroviruses coverage includes:
HIV cure research
HIV prevention science
- Vaccine research
- Systemic and Topical PreP
Molecular and cell biology of HIV and SIV
Developments in HIV pathogenesis and comorbidities
Molecular biology, immunology, and epidemiology of HTLV
Pharmacology of HIV therapy
Social and behavioral science
Rapid publication of emerging sequence information.