High level of HIV drug resistance informs dolutegravir roll-out and optimized NRTI backbone strategy in Mozambique

Author:

Carnimeo V1ORCID,Pulido Tarquino I A2,Fuentes S12,Vaz D3,Molfino L3,Tamayo Antabak N3,Cuco R M4,Couto A5,Lobo S6,de Amaral Fidelis J7,Mulassua J S7,Ciglenecki I8,Ellman T9,Schramm B1

Affiliation:

1. Epicentre, Paris, France

2. Médecins Sans Frontières Belgium, Mozambique Mission

3. Médecins Sans Frontières Switzerland, Mozambique Mission

4. National Directorate of Public Health, Ministry of Health, Maputo, Mozambique

5. Ministry of Health of Mozambique, Maputo, Mozambique

6. Health Directorate of Maputo, Maputo, Mozambique

7. Provincial Health directorate, Tete, Mozambique

8. Médecins Sans Frontières, Geneva, Switzerland

9. Médecins Sans Frontières, Southern Africa Medical Unit (SAMU), South Africa

Abstract

Abstract Background HIV drug resistance (HIV-DR) is rising in sub-Saharan Africa in both ART-naive and ART-experienced patients. Objectives To estimate the level of acquired DR (ADR) and pre-treatment DR (PDR) across selected urban and rural sites in Southern Africa, in Mozambique. Methods We conducted two cross-sectional surveys among adult HIV patients (October 2017–18) assessing ADR and PDR. In the (ADR) survey, those on NNRTI-based first-line ART for ≥6 months were recruited (three sites). In the PDR survey, those ART-naive or experienced with ≥3 months of treatment interruption prior were enrolled (eight sites). Results Among 1113 ADR survey participants 83% were receiving tenofovir (TDF)/lamivudine (3TC)/efavirenz (EFV). The median time on ART was 4.5 years (Maputo) and 3.2 years (Tete), 8.3% (95% CI 6.2%-10.6%, Maputo) and 15.5% (Tete) had a VL ≥ 1000 copies/mL, among whom 66% and 76.4% had NNRTI+NRTI resistance, and 52.8% and 66.7% had 3TC+TDF-DR. Among those on TDF regimens, 31.1% (Maputo) and 42.2% (Tete) were still TDF susceptible, whereas 24.4% and 11.5% had TDF+zidovudine (ZDV)-DR. Among those on ZDV regimens, 25% and 54.5% had TDF+ZDV-DR. The PDR survey included 735 participants: NNRTI-PDR was 16.8% (12.0–22.6) (Maputo) and 31.2% (26.2–36.6) (Tete), with a higher proportion (≥50%) among those previously on ART affected by PDR. Conclusions In Mozambique, viral failure was driven by NNRTI and NRTI resistance, with NRTI DR affecting backbone options. NNRTI-PDR levels surpassed the WHO 10% ‘alert’ threshold. Replacing NNRTI first-line drugs is urgent, as is frequent viral load monitoring and resistance surveillance. Changing NRTI backbones when switching to second-line regimens may need reconsideration.

Funder

Médecins Sans Frontières

Publisher

Oxford University Press (OUP)

Subject

General Medicine

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