Herpes Simplex Virus Type 2 Infection Does Not Influence Viral Dynamics during Early HIV‐1 Infection
1University of California, San Diego, La Jolla, and 2Veterans Affairs San Diego Healthcare System, San Diego
Objective.
We sought to compare baseline and longitudinal plasma HIV‐1 loads between herpes simplex virus type 2 (HSV‐2)–seropositive and –seronegative individuals who are enrolled in a primary HIV‐1 infection cohort in San Diego, California.
Design.
The study was a retrospective cohort analysis.
Methods.
We categorized antiretroviral‐naive subjects on the basis of HSV‐2 serostatus at baseline using an HSV‐2 enzyme immunoassay. Low positive results (1.1–3.5) were confirmed by Western blotting. We compared baseline HIV‐1 loads of the 2 groups using a linear model. To detect differences in HIV‐1 dynamics, we analyzed longitudinal viral loads using a flexible semiparametric model, controlling for the time to antiretroviral therapy and stratifying by HIV‐1 infection stage at entry.
Results.
We studied 294 adult men. Ninety percent reported sex with men as their main HIV‐1 risk factor. The seroprevalence of HSV‐2 was 41.5%. The HSV‐2–seropositive and –seronegative groups had similar baseline HIV‐1 loads during acute infection (5.52 vs. 5.72 log10 copies/mL;
) and early infection (4.57 vs. 4.67 log10 copies/mL;
). Longitudinally, the difference in HIV‐1 loads between HSV‐2–seropositive and –seronegative men remained close to 0 during the first year of infection.
Conclusions.
HSV‐2 serostatus has minimal influence on the dynamics of HIV‐1 during acute and early HIV‐1 infection.
Received 25 September 2006; accepted 1 November 2006; electronically published 15 March 2007.
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(See the editorial commentary by Corey, on pages 1242–4, and the article by Kapiga et al., on pages 1260–9.)
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Online publication date: 1-Aug-2009.
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Online publication date: 15-May-2008.
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Online publication date: 1-May-2007.
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Potential conflicts of interest: none reported.
Financial support: Bristol‐Myers Squibb (2005 Fellow Virology Research Award Program); National Institutes of Health (grants AI27670, AI43638, AI36214 [to the University of California, San Diego Center for AIDS Research], AI29164, AI47745, AI57167, and 5k23‐AI55276); Research Center for AIDS and HIV Infection, Veterans Affairs San Diego Healthcare System.





