Prevalence of doravirine-associated resistance mutations in HIV-1-infected antiretroviral-experienced patients from two large databases in France and Italy.


Journal

The Journal of antimicrobial chemotherapy
ISSN: 1460-2091
Titre abrégé: J Antimicrob Chemother
Pays: England
ID NLM: 7513617

Informations de publication

Date de publication:
01 04 2020
Historique:
received: 29 08 2019
revised: 25 11 2019
accepted: 11 12 2019
pubmed: 25 1 2020
medline: 25 6 2021
entrez: 25 1 2020
Statut: ppublish

Résumé

Doravirine, a novel NNRTI, selects for specific mutations in vitro, including mutations at reverse transcriptase (RT) positions 106, 108, 188, 227, 230 and 234. The aim of this study was to examine the prevalence of doravirine-associated resistance mutations in HIV-1-infected antiretroviral-experienced patients. Doravirine-associated resistance mutations identified in vitro or in vivo were studied in a set of 9199 HIV-1 RT sequences from HIV-1 antiretroviral-experienced patients, including 381 NNRTI-failing patients in France and Italy between 2012 and 2017. The following mutations were considered as resistance mutations: V106A/M, V108I, Y188L, G190S, F227C/L/V, M230I/L, L234I, P236L, K103N + Y181C, K103N + P225H and K103N + L100I. The frequencies of doravirine-associated resistance mutations (total dataset versus NNRTI-failing patients) were: V106A/M, 0.8% versus 2.6%; V108I, 3.3% versus 9.2%; Y188L, 1.2% versus 2.6%; G190S, 0.3% versus 2.1%; F227C/L/V, 0.5% versus 1.8%; M230I/L, 2.8% versus 0%; L234I, 0.1% versus 0.5%; K103N + Y181C, 3.9% versus 3.9%; K103N + P225H, 2.9% versus 4.7%; and K103N + L100I, 1.7% versus 3.9%, with a significantly higher proportion of these mutations in the NNRTI-failing group (P < 0.05), except for M230I/L and K103N + Y181C. The overall prevalence of sequences with at least one doravirine-associated resistance mutation was 12.2% and 34.9% in the total dataset and NNRTI-failing patients (P < 0.001), respectively. In comparison, the prevalence of the common NNRTI mutations V90I, K101E/P, K103N/S, E138A/G/K/Q/R/S, Y181C/I/V and G190A/E/S/Q were higher (8.9%, 7.9%, 28.6%, 12.6%, 14.2% and 8.9%, respectively). These results suggest that doravirine resistance in antiretroviral-experienced patients generally and specifically among NNRTI-failing patients is lower than resistance to other NNRTIs currently used, confirming its distinguishing resistance pattern.

Identifiants

pubmed: 31976534
pii: 5715476
doi: 10.1093/jac/dkz553
doi:

Substances chimiques

Anti-HIV Agents 0
Pyridones 0
Reverse Transcriptase Inhibitors 0
Triazoles 0
doravirine 913P6LK81M
HIV Reverse Transcriptase EC 2.7.7.49

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1026-1030

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

Cathia Soulie (C)

Sorbonne Université, INSERM, UMR_S 1136 Pierre Louis Institute of Epidemiology and Public Health, AP-HP, Hôpital Pitié Salpêtrière, Laboratoire de Virologie, Paris, France.

Maria Mercedes Santoro (MM)

Department of Experimental Medicine, University of Rome "Tor Vergata", Rome, Italy.

Alexandre Storto (A)

Université de Paris, INSERM, UMR 1137 IAME, F-75018 Paris, France.

Basma Abdi (B)

Sorbonne Université, INSERM, UMR_S 1136 Pierre Louis Institute of Epidemiology and Public Health, AP-HP, Hôpital Pitié Salpêtrière, Laboratoire de Virologie, Paris, France.

Charlotte Charpentier (C)

Université de Paris, INSERM, UMR 1137 IAME, F-75018 Paris, France.
Laboratoire de Virologie, AP-HP, Hôpital Bichat-Claude Bernard, F-75018 Paris, France.

Daniele Armenia (D)

Department of Experimental Medicine, University of Rome "Tor Vergata", Rome, Italy.
UniCamillus, Saint Camillus International University of Health Sciences, Rome, Italy.

Aude Jary (A)

Sorbonne Université, INSERM, UMR_S 1136 Pierre Louis Institute of Epidemiology and Public Health, AP-HP, Hôpital Pitié Salpêtrière, Laboratoire de Virologie, Paris, France.

Federica Forbici (F)

National Institute for Infectious Diseases L. Spallanzani, IRCCS, Rome, Italy.

Ada Bertoli (A)

Department of Experimental Medicine, University of Rome "Tor Vergata", Rome, Italy.

William Gennari (W)

Clinic of Infectious Diseases, Modena University Hospital, Modena, Italy.

Massimo Andreoni (M)

Department of Clinical Infectious Diseases, University Hospital of Rome Tor Vergata, Rome, Italy.

Cristina Mussini (C)

Clinic of Infectious Diseases, Modena University Hospital, Modena, Italy.

Andrea Antinori (A)

National Institute for Infectious Diseases L. Spallanzani, IRCCS, Rome, Italy.

Carlo Federico Perno (CF)

National Institute for Infectious Diseases L. Spallanzani, IRCCS, Rome, Italy.

Vincent Calvez (V)

Sorbonne Université, INSERM, UMR_S 1136 Pierre Louis Institute of Epidemiology and Public Health, AP-HP, Hôpital Pitié Salpêtrière, Laboratoire de Virologie, Paris, France.

Francesca Ceccherini-Silberstein (F)

Department of Experimental Medicine, University of Rome "Tor Vergata", Rome, Italy.

Diane Descamps (D)

Université de Paris, INSERM, UMR 1137 IAME, F-75018 Paris, France.
Laboratoire de Virologie, AP-HP, Hôpital Bichat-Claude Bernard, F-75018 Paris, France.

Anne-Genevieve Marcelin (AG)

Sorbonne Université, INSERM, UMR_S 1136 Pierre Louis Institute of Epidemiology and Public Health, AP-HP, Hôpital Pitié Salpêtrière, Laboratoire de Virologie, Paris, France.

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Classifications MeSH