Resistance levels to non-nucleoside reverse transcriptase inhibitors among pregnant women with recent HIV infection in Malawi

Author:

Bello George12ORCID,Kagoli Matthew1,Chipeta Sikhona1,Auld Andrew3,Chang Joy C-W4,DeVos Joshua R3ORCID,Kim Evelyn3,Mkungudza Jonathan12,Payne Danielle3,Eliya Michael1,Nyirenda Rose1,Jahn Andreas12,Mzumara Taziona1,Mvula Bernard1,Dadabhai Sufia5,Namakhoma Ireen2,Babaye Yusuf2,Giron Amalia6,Jordan Michael R7,Bertagnolio Silvia6,O’Malley Gabrielle8,Wadonda-Kabondo Nellie3

Affiliation:

1. Malawi Ministry of Health, Lilongwe, Malawi

2. International Training & Education Centre for Health (I-TECH), Lilongwe, Malawi

3. Centers for Disease Control and Prevention Malawi

4. Centers for Disease Control and Prevention, Atlanta, GA, USA

5. John Hopkins Research Project Malawi, Lilongwe, Malawi

6. World Health Organization, Geneva, Switzerland

7. Tufts University School of Medicine, Boston, MA, USA

8. International Training & Education Centre for Health (I-TECH), Seattle, WA, USA

Abstract

Background Information on HIV drug resistance (HIVDR) prevalence in people newly diagnosed with HIV is limited. We implemented a cross-sectional study to estimate HIVDR prevalence among pregnant women recently infected with HIV in Malawi. Methods The HIVDR study was nested within a routine antenatal clinic (ANC) sentinel surveillance survey. Dried blood spot samples were tested for recent infection using a limiting antigen antibody assay together with HIV viral load testing. HIV-1 protease and reverse transcriptase were sequenced using Sanger sequencing. Drug susceptibility was predicted using Stanford HIVdb algorithm (version 8.9). Weighted analysis was performed in Stata 15.1. Results Of the 21,642 pregnant women enrolled in the ANC survey, 8.4% (1826/21,642) tested HIV positive. Of these, 5.0% (92/1826) had recent HIV infection, and 90.2% (83/92) were tested by PCR. The amplification and sequencing success rate was 57.8% (48/83). The prevalence of any HIVDR was 14.6% (5/45) (95% CI: 4.7–36.8%), all of which indicated HIVDR to nonnucleoside reverse transcriptase inhibitors (NNRTIs). HIVDR to nucleoside reverse transcriptase inhibitors was 7.9% (2/45) (95% CI: 1.4–34.6%). Resistance to protease inhibitors currently in use in Malawi was not observed. Conclusions Despite the low number of cases with presumed TDR, our study hints that resistance to NNRTIs was high, above the 10% target for regimen change. Further investigation is needed to establish the exact magnitude of presumed TDR among women recently infected with HIV. These findings support the transition to an integrase inhibitor-based first-line regimen for patients initiating or on ART.

Funder

Center for Global Health

Publisher

SAGE Publications

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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