Drug Resistance Mutations Among South African Children Living With HIV on WHO-recommended ART Regimens.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
05 10 2021
Historique:
received: 18 02 2020
pubmed: 1 8 2020
medline: 21 10 2021
entrez: 1 8 2020
Statut: ppublish

Résumé

Children living with human immunodeficiency virus (HIV) (CLHIV) receiving antiretroviral therapy (ART) in resource-limited settings are susceptible to high rates of acquired HIV drug resistance (HIVDR), but few studies include children initiating age-appropriate World Health Organization (WHO)-recommended first-line regimens. We report data from a cohort of ART-naive South African children who initiated first-line ART. ART-eligible CLHIV aged 0-12 years were enrolled from 2012 to 2014 at 5 public South African facilities and were followed for up to 24 months. Enrolled CLHIV received standard-of-care WHO-recommended first-line ART. At the final study visit, a dried blood spot sample was obtained for viral load and genotypic resistance testing. Among 72 successfully genotyped CLHIV, 49 (68.1%) received ABC/3TC/LPV/r, and 23 (31.9%) received ABC/3TC/EFV. All but 2 children on ABC/3TC/LPV/r were <3 years, and all CLHIV on ABC/3TC/EFV were ≥3 years. Overall, 80.6% (58/72) had at least one drug resistance mutation (DRM). DRMs to nonnucleoside reverse transcriptase inhibitors (NNRTIs) and nucleoside reverse transcriptase inhibitors (NRTIs) were found among 65% and 51% of all CLHIV, respectively, with no statistical difference by ART regimen. More CLHIV on ABC/3TC/EFV, 47.8% (11/23), were found to have 0 or only 1 effective antiretroviral drug remaining in their current regimen compared to 8.2% (4/49) on ABC/3TC/LPV/r. High levels of NNRTI and NRTI DRMs among CLHIV receiving ABC/3TC/LPV/r suggests a lasting impact of failed mother-to-child transmission interventions on DRMs. However, drug susceptibility analysis reveals that CLHIV with detectable viremia on ABC/3TC/LPV/r are more likely to have maintained at least 2 effective agents on their current HIV regimen than those on ABC/3TC/EFV.

Sections du résumé

BACKGROUND
Children living with human immunodeficiency virus (HIV) (CLHIV) receiving antiretroviral therapy (ART) in resource-limited settings are susceptible to high rates of acquired HIV drug resistance (HIVDR), but few studies include children initiating age-appropriate World Health Organization (WHO)-recommended first-line regimens. We report data from a cohort of ART-naive South African children who initiated first-line ART.
METHODS
ART-eligible CLHIV aged 0-12 years were enrolled from 2012 to 2014 at 5 public South African facilities and were followed for up to 24 months. Enrolled CLHIV received standard-of-care WHO-recommended first-line ART. At the final study visit, a dried blood spot sample was obtained for viral load and genotypic resistance testing.
RESULTS
Among 72 successfully genotyped CLHIV, 49 (68.1%) received ABC/3TC/LPV/r, and 23 (31.9%) received ABC/3TC/EFV. All but 2 children on ABC/3TC/LPV/r were <3 years, and all CLHIV on ABC/3TC/EFV were ≥3 years. Overall, 80.6% (58/72) had at least one drug resistance mutation (DRM). DRMs to nonnucleoside reverse transcriptase inhibitors (NNRTIs) and nucleoside reverse transcriptase inhibitors (NRTIs) were found among 65% and 51% of all CLHIV, respectively, with no statistical difference by ART regimen. More CLHIV on ABC/3TC/EFV, 47.8% (11/23), were found to have 0 or only 1 effective antiretroviral drug remaining in their current regimen compared to 8.2% (4/49) on ABC/3TC/LPV/r.
CONCLUSIONS
High levels of NNRTI and NRTI DRMs among CLHIV receiving ABC/3TC/LPV/r suggests a lasting impact of failed mother-to-child transmission interventions on DRMs. However, drug susceptibility analysis reveals that CLHIV with detectable viremia on ABC/3TC/LPV/r are more likely to have maintained at least 2 effective agents on their current HIV regimen than those on ABC/3TC/EFV.

Identifiants

pubmed: 32735012
pii: 5878919
doi: 10.1093/cid/ciaa1068
doi:

Substances chimiques

Anti-HIV Agents 0

Types de publication

Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2217-e2225

Subventions

Organisme : U.S. President's Emergency Plan for AIDS Relief
Organisme : CDC HHS
ID : 5U62PS223540
Pays : United States

Informations de copyright

Published by Oxford University Press for the Infectious Diseases Society of America 2020.

Auteurs

Stephanie Hackett (S)

US Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

Chloe A Teasdale (CA)

Department of Epidemiology and Biostatistics, CUNY Graduate School of Public Health & Health Policy, New York, USA.
ICAP at Columbia University, Mailman School of Public Health, Columbia University, New York, New York, USA.
Department of Epidemiology, Mailman School of Public Health, Columbia University, New York, New York, USA.

Sherri Pals (S)

US Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

Anthony Muttiti (A)

ICAP at Columbia University, Mailman School of Public Health, Columbia University, New York, New York, USA.

Mary Mogashoa (M)

US Centers for Disease Control and Prevention, Pretoria, South Africa.

Joy Chang (J)

US Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

Clement Zeh (C)

US Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

Artur Ramos (A)

US Centers for Disease Control and Prevention, Maputo, Mozambique.

Emilia D Rivadeneira (ED)

US Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

Joshua DeVos (J)

US Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

Katrina Sleeman (K)

US Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

Elaine J Abrams (EJ)

ICAP at Columbia University, Mailman School of Public Health, Columbia University, New York, New York, USA.
Department of Epidemiology, Mailman School of Public Health, Columbia University, New York, New York, USA.
Department of Pediatrics, Vagelos College of Physicians & Surgeons, Columbia University, New York, New York, USA.

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