Impact of Herpes Simplex Virus Type 2 on HIV-1 Acquisition and Progression in an HIV Vaccine Trial (the Step Study)
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Introduction: Extensive observational data suggest that herpes simplex virus type 2 (HSV-2) infection may facilitate HIV acquisition, increase HIV viral load, and accelerate HIV progression and onward transmission. To explore these relationships, we examined the impact of preexisting HSV-2 infection in an international HIV vaccine trial.
Methods: We analyzed the associations between prevalent HSV-2 infection and HIV-1 acquisition and progression among 1836 men who have sex with men. We used Cox proportional hazards regression models to estimate the association between HSV-2 infection and both HIV acquisition and antiretroviral therapy (ART) initiation, and linear regression to explore the effect of HSV-2 on pre-ART viral load.
Results: HSV-2 infection increased risk of HIV-1 acquisition among all volunteers [adjusted hazard ratio 2.2; 95% confidence interval (CI): 1.4 to 3.5]. Adjusting for demographic variables, circumcision, Ad5 titer, and significant risk behaviors, the risk of HIV acquisition among HSV-2-infected placebo recipients was 3-fold higher than HSV-2 seronegatives (adjusted hazard ratio 3.3; 95% CI: 1.6 to 6.9). Past HSV-2 infection was associated with a 0.2 log10 copies per milliliter higher adjusted mean set point viral load (95% CI: 0.3 lower to 0.6 higher). HSV-2 infection was not associated with time to ART initiation.
Conclusions: Among men who have sex with men in an HIV-1 vaccine trial, preexisting HSV-2 infection was a major risk factor for HIV acquisition. Past HSV-2 did not significantly increase HIV viral load or early disease progression. HSV-2-seropositive persons will likely prove more difficult than HSV-2-seronegative persons to protect against HIV infection using vaccines or other prevention strategies.
Wang J, Huang M, Du Y, Chen H, Li Z, Zhai T Probiotics Antimicrob Proteins. 2023; 16(6):1966-1978.
PMID: 37624569 PMC: 11573810. DOI: 10.1007/s12602-023-10137-8.
Osinachi Ogu C, Uwadiegwu Achukwu P, Onubiwe Nkwo P, Ifeoma-Ossy Ogu R, Steven Onwukwe O, Chinonye Azubuike N Curr HIV Res. 2022; 20(6):463-471.
PMID: 36380408 DOI: 10.2174/1570162X21666221114102411.
Contribution of Sex Differences to HIV Immunology, Pathogenesis, and Cure Approaches.
Moran J, Turner S, Marsden M Front Immunol. 2022; 13:905773.
PMID: 35693831 PMC: 9174895. DOI: 10.3389/fimmu.2022.905773.
The Contribution of Human Herpes Viruses to γδ T Cell Mobilisation in Co-Infections.
Martini F, Champagne E Viruses. 2021; 13(12).
PMID: 34960641 PMC: 8704314. DOI: 10.3390/v13122372.
Zhang J, Huang X, Tang W, Chu Z, Hu Q, Liu J Front Immunol. 2021; 12:712802.
PMID: 34367176 PMC: 8339583. DOI: 10.3389/fimmu.2021.712802.