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  5. Limited emergence of resistance to integrase strand transfer inhibitors (INSTIs) in ART-experienced participants failing dolutegravir-based antiretroviral therapy: a cross-sectional analysis of a Northeast Nigerian cohort
 
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Limited emergence of resistance to integrase strand transfer inhibitors (INSTIs) in ART-experienced participants failing dolutegravir-based antiretroviral therapy: a cross-sectional analysis of a Northeast Nigerian cohort
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Limited emergence of resistance to integrase strand transfer inhibitors (INSTIs) in ART-experienced participants failing dol.pdf (601.73 KB)
Published version
Author(s)
Abdullahi, Adam
Kida, Ibrahim Musa
Maina, Umar Abdullahi
Ibrahim, Amina Husaini
Mshelia, James
more
Type
Journal Article
Abstract
Background
Due to the high prevalence of resistance to NNRTI-based ART since 2018, consolidated recommendations from the WHO have indicated dolutegravir as the preferred drug of choice for HIV treatment globally. There is a paucity of resistance outcome data from HIV-1 non-B subtypes circulating across West Africa.

Aims
We characterized the mutational profiles of persons living with HIV from a cross-sectional cohort in North-East Nigeria failing a dolutegravir-based ART regimen.

Methods
WGS of plasma samples collected from 61 HIV-1-infected participants following virological failure of dolutegravir-based ART were sequenced using the Illumina platform. Sequencing was successfully completed for samples from 55 participants. Following quality control, 33 full genomes were analysed from participants with a median age of 40 years and median time on ART of 9 years. HIV-1 subtyping was performed using SNAPPy.

Results
Most participants had mutational profiles reflective of exposure to previous first- and second-line ART regimens comprised NRTIs and NNRTIs. More than half of participants had one or more drug resistance-associated mutations (DRMs) affecting susceptibility to NRTIs (17/33; 52%) and NNRTIs (24/33; 73%). Almost a quarter of participants (8/33; 24.4%) had one or more DRMs affecting tenofovir susceptibility. Only one participant, infected with HIV-1 subtype G, had evidence of DRMs affecting dolutegravir susceptibility—this was characterized by the T66A, G118R, E138K and R263K mutations.

Conclusions
This study found a low prevalence of resistance to dolutegravir; the data are therefore supportive of the continual rollout of dolutegravir as the primary first-line regimen for ART-naive participants and the preferred switch to second-line ART across the region. However, population-level, longer-term data collection on dolutegravir outcomes are required to further guide implementation and policy action across the region.
Date Issued
2023-08
Date Acceptance
2023-05-30
Citation
Journal of Antimicrobial Chemotherapy, 2023, 78 (8), pp.2000-2007
URI
http://hdl.handle.net/10044/1/107064
URL
https://academic.oup.com/jac/article/78/8/2000/7208628
DOI
https://www.dx.doi.org/10.1093/jac/dkad195
ISSN
0305-7453
Publisher
Oxford University Press
Start Page
2000
End Page
2007
Journal / Book Title
Journal of Antimicrobial Chemotherapy
Volume
78
Issue
8
Copyright Statement
© The Author(s) 2023. Published by Oxford University Press on behalf of British Society for Antimicrobial Chemotherapy.
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
License URL
https://creativecommons.org/licenses/by/4.0/
Identifier
https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:001013920600001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=a2bf6146997ec60c407a63945d4e92bb
Subjects
EFAVIRENZ
HIGH-PREVALENCE
HIV-1 DRUG-RESISTANCE
INFECTION
Infectious Diseases
INITIAL TREATMENT
Life Sciences & Biomedicine
Microbiology
MULTICENTER
MUTATION
Pharmacology & Pharmacy
REGIMENS
Science & Technology
SUB-SAHARAN AFRICA
VIROLOGICAL FAILURE
Publication Status
Published
Date Publish Online
2023-06-27
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