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Effect of HSV-2 infection on subsequent HIV acquisition: an updated systematic review and meta-analysis - 23/11/17

Doi : 10.1016/S1473-3099(17)30405-X 
Katharine J Looker, PhD a, , , Jocelyn A R Elmes, PhD c, , Sami L Gottlieb, MD d, Joshua T Schiffer, MD e, f, Peter Vickerman, ProfDPhil a, Katherine M E Turner, PhD b, Marie-Claude Boily, ProfPhD c
a School of Social and Community Medicine, University of Bristol, Bristol, UK 
b Bristol Veterinary School, University of Bristol, Bristol, UK 
c Department of Infectious Disease Epidemiology, Imperial College London, London, UK 
d Department of Reproductive Health and Research, World Health Organization, Geneva, Switzerland 
e Vaccine and Infectious Disease Division, and Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA 
f Department of Medicine, University of Washington, Seattle, WA, USA 

* Correspondence to: Dr Katharine J Looker, School of Social and Community Medicine, University of Bristol, Bristol BS8 2BN, UK Correspondence to: Dr Katharine J Looker School of Social and Community Medicine University of Bristol Bristol BS8 2BN UK

Summary

Background

HIV and herpes simplex virus type 2 (HSV-2) infections cause a substantial global disease burden and are epidemiologically correlated. Two previous systematic reviews of the association between HSV-2 and HIV found evidence that HSV-2 infection increases the risk of HIV acquisition, but these reviews are now more than a decade old.

Methods

For this systematic review and meta-analysis, we searched PubMed, MEDLINE, and Embase (from Jan 1, 2003, to May 25, 2017) to identify studies investigating the risk of HIV acquisition after exposure to HSV-2 infection, either at baseline (prevalent HSV-2 infection) or during follow-up (incident HSV-2 infection). Studies were included if they were a cohort study, controlled trial, or case-control study (including case-control studies nested within a cohort study or clinical trial); if they assessed the effect of pre-existing HSV-2 infection on HIV acquisition; and if they determined the HSV-2 infection status of study participants with a type-specific assay. We calculated pooled random-effect estimates of the association between prevalent or incident HSV-2 infection and HIV seroconversion. We also extended previous investigations through detailed meta-regression and subgroup analyses. In particular, we investigated the effect of sex and risk group (general population vs higher-risk populations) on the relative risk (RR) of HIV acquisition after prevalent or incident HSV-2 infection. Higher-risk populations included female sex workers and their clients, men who have sex with men, serodiscordant couples, and attendees of sexually transmitted infection clinics.

Findings

We identified 57 longitudinal studies exploring the association between HSV-2 and HIV. HIV acquisition was almost tripled in the presence of prevalent HSV-2 infection among general populations (adjusted RR 2·7, 95% CI 2·2–3·4; number of estimates [Ne]=22) and was roughly doubled among higher-risk populations (1·7, 1·4–2·1; Ne=25). Incident HSV-2 infection in general populations was associated with the highest risk of acquisition of HIV (4·7, 2·2–10·1; Ne=6). Adjustment for confounders at the study level was often incomplete but did not significantly affect the results. We found moderate heterogeneity across study estimates, which was explained by risk group, world region, and HSV-2 exposure type (prevalent vs incident).

Interpretation

We found evidence that HSV-2 infection increases the risk of HIV acquisition. This finding has important implications for management of individuals diagnosed with HSV-2 infection, particularly for those who are newly infected. Interventions targeting HSV-2, such as new HSV vaccines, have the potential for additional benefit against HIV, which could be particularly powerful in regions with a high incidence of co-infection.

Funding

World Health Organization.

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© 2017  World Health Organization. Publié par Elsevier Masson SAS. Tous droits réservés.
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Vol 17 - N° 12

P. 1303-1316 - décembre 2017 Retour au numéro
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