Abstract

BackgroundFemale sex workers (FSWs) at substantial risk of HIV are potentially a suitable group for HIV prevention trials including vaccine trials. Few HIV vaccine preparatory studies have been conducted among FSWs in Sub-Saharan Africa (SSA); data are therefore limited on acceptability of vaccine trial procedures. We determined vaccination completion and one-year retention among FSWs in Kampala, Uganda.MethodsWe conducted a prospective study that simulated a vaccine efficacy trial among HIV negative FSWs (18–49 years). Hepatitis B vaccine (Engerix B) was used to mimic an HIV vaccine product. Volunteers received 1 ml intramuscular injection at 0, 1 and 6 months, and made additional visits (3 days post-vaccination and months 3, 9 and 12). They were censored at that visit if diagnosed as HIV positive or pregnant. We collected socio-demographic, behavioral and clinical data at baseline, 6 and 12 months and fitted Poisson regression models with robust standard error to find factors associated with vaccination completion and retention.ResultsWe enrolled 290 volunteers (median age 27 years) of whom 230 reached a study end-point as follows: 7 became HIV infected, 11 became pregnant and 212 completed both the vaccination schedule and 12-month visit giving a retention of 77.9% (212/272). Vaccination completion was 82.4%.Non-retention at 1 year was more likely among those reporting symptoms of genital ulcer disease (GUD) in the past 3 months (IRR 1.90; 95% CI 1.09–3.32) and those < 35 years; (IRR 6.59; 95% CI 2.11–20.57). Non-completion of the vaccination schedule was associated with being < 35 years (IRR 13.10; 95% CI 1.89–90.92, reporting GUD symptoms (IRR 3.02; 95% CI 1.71–5.33) and reporting consistent condom use with new sexual partners (IRR 2.57; 95% CI 1.10–6.07).ConclusionsFSWs are at substantial risk of HIV infection and yet willing to participate in HIV vaccine and prevention research; young FSWs should be empowered, and those reporting GUD symptoms need close follow up to improve participation in future HIV vaccine trials.

Highlights

  • Female sex workers (FSWs) at substantial risk of HIV are potentially a suitable group for HIV prevention trials including vaccine trials

  • Baseline characteristics of FSWs enrolled in the simulated vaccine efficacy trial (SiVET) study in Kampala, Uganda We screened 381 volunteers for the study of whom 304 (79.8%) were eligible and 290 (76.1%) enrolled

  • FSWs in Kampala are at substantial risk of HIV infection and are willing to be enrolled in HIV vaccine and prevention research; younger FSWs may be harder to retain

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Summary

Introduction

Female sex workers (FSWs) at substantial risk of HIV are potentially a suitable group for HIV prevention trials including vaccine trials. Few HIV vaccine preparatory studies have been conducted among FSWs in Sub-Saharan Africa (SSA); data are limited on acceptability of vaccine trial procedures. The modified vaccine in HIVTN100 elicited sufficiently high immune responses and, pre-specified immunological go/no-go criteria were achieved leading to initiation of an efficacy trial (HVTN702) [3, 6]. With the on-going HPTN084 trial comparing efficacy of long acting injectable cabotegravir and oral PrEP (Tenofovir Disoproxyl Fumarate /Emtricitabine), it is evident that several biomedical HIV prevention products may soon be available; it is for this reason that researchers in the International AIDS Vaccine Initiative (IAVI) network in SSA are preparing suitable populations for future HIV prevention efficacy trials of interventions such as long acting anti-retroviral drugs, protective antibodies and vaccines

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