Abstract

BackgroundThe inadequacy of HIV viraemia and resistance monitoring in Africa leads to uncontrolled circulation of HIV strains with drug resistance mutations (DRM), compromising antiretroviral therapy (ART) effectiveness. This study describes the DRM prevalence and its therapeutic impact in HIV-infected pediatric patients from Kinshasa (Democratic Republic of Congo, DRC).MethodsFrom 2016–2018, dried blood were collected from 71 HIV-infected children and adolescents under ART in two hospitals in Kinshasa for HIV-1 DRM pol analysis, predicted ARV-susceptibility by Stanford and phylogenetic characterization.ResultsHIV-1 sequences were recovered from 55 children/adolescents with 14 years of median-age. All had received nucleoside and non-nucleoside reverse transcriptase inhibitors (NRTI, NNRTI), 9.1% protease inhibitors (PI) and only one integrase inhibitor (INI). Despite the use of ART, 89.1% showed virological failure and 67.3% carried viruses with major-DRM to one (12.7%), two (47.3%), or three (5.5%) ARV-families. Most children/adolescents harbored DRM to NNRTI (73.5%) or NRTI (61.2%). Major-DRM to PI was present in 8.3% and minor-DRM to INI in 15%. Dual-class-NRTI+NNRTI resistance appeared in 53.1% of patients. Viruses presented high/intermediate resistance to nevirapine (72.9% patients), efavirenz (70.9%), emtricitabine/lamivudine (47.9%), rilpivirine (41.7%), etravirine (39.6%), doravidine (33.3%), zidovudine (22.9%), among others. Most participants were susceptible to INI and PI. Great diversity of variants was found, with a high rate (40%) of unique recombinants.ConclusionThe high DRM prevalence observed among HIV-infected children and adolescents in Kinshasa could compromise the 95-95-95-UNAIDS targets in the DRC. It also reinforces the need for routine resistance monitoring for optimal rescue therapy election in this vulnerable population to control the spread of resistant HIV in the country.

Highlights

  • Over the last years, scale-up of HIV antiretroviral treatment (ART) has had a major impact on HIV-related illness, averting AIDS-related deaths, preventing new HIV infections, and resulting in cost savings [1]

  • This study describes the drug resistance mutations (DRM) prevalence and its therapeutic impact in HIV-infected pediatric patients from Kinshasa (Democratic Republic of Congo, DRC)

  • Major-DRM to protease inhibitors (PI) was present in 8.3% and minorDRM to INI in 15%

Read more

Summary

Introduction

Scale-up of HIV antiretroviral treatment (ART) has had a major impact on HIV-related illness, averting AIDS-related deaths, preventing new HIV infections, and resulting in cost savings [1]. Since non-nucleoside reverse transcriptase inhibitors (NNRTI) based ART continues to be used in first-line ART in the DRC as in many Sub-Saharan Africa countries, an increase in pre-antiretroviral-treatment drug resistance (PDR) to NNRTI over 10% is expected in this region over the 15 years. This PDR rate will be responsible for 16% of AIDS deaths and 9% of new HIV infections in Sub-Saharan Africa in 2016–2030 [5]. This study describes the DRM prevalence and its therapeutic impact in HIV-infected pediatric patients from Kinshasa (Democratic Republic of Congo, DRC)

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call