HIV-1 RNA Kinetics in Blood Plasma and in Seminal Plasma of Men Starting a Dolutegravir-Based Triple-Combination Regimen at the Time of Primary HIV-1 Infection.


Journal

The Journal of infectious diseases
ISSN: 1537-6613
Titre abrégé: J Infect Dis
Pays: United States
ID NLM: 0413675

Informations de publication

Date de publication:
05 01 2022
Historique:
received: 04 04 2021
accepted: 22 06 2021
pubmed: 25 6 2021
medline: 24 2 2022
entrez: 24 6 2021
Statut: ppublish

Résumé

We compared the proportion of participants achieving first undetectable HIV-1 RNA (VL) in seminal plasma (SP) and blood plasma (BP) in 19 men starting dolutegravir-based regimen at primary HIV infection. At baseline, median VL was 6.5 (interquartile range [IQR], 5.6-7.9) and 4.5 (IQR, 3.5-5.0) log10 copies/mL in BP and SP, respectively. Between baseline and week 48, significantly higher proportion of participants achieved first VL below limit of quantification in SP (93.0%) than in BP (84.2%; P = .008). Time to first undetectable VL was 8 weeks in SP (95% confidence interval [CI], 5.6-10.4) and 24 weeks in BP (95% CI, 14.1-33.9).

Identifiants

pubmed: 34166492
pii: 6309026
doi: 10.1093/infdis/jiab336
doi:

Substances chimiques

Anti-HIV Agents 0
Heterocyclic Compounds, 3-Ring 0
Oxazines 0
Piperazines 0
Pyridones 0
RNA, Viral 0
dolutegravir DKO1W9H7M1

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

116-120

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

Auteurs

Jade Ghosn (J)

Service de Maladies Infectieuses, Hôpital Bichat, Infection Modelisation Antimicrobial Evolution, UMR1137, INSERM, Université de Paris, Paris, France.

Lambert Assoumou (L)

INSERM, Sorbonne Université, Institut Pierre Louis d'Epidémiologie et de Santé Publique, Paris, France.

Caroline Lascoux-Combe (C)

Service de Maladies Infectieuses, Hôpital Saint Louis, AP-HP, Paris, France.

Gilles Peytavin (G)

Service de Pharmacologie et Toxicologie, Hôpital Bichat, AP-HP, Infection Modelisation Antimicrobial Evolution, INSERM UMR1137, UF301, Université de Paris, Paris, France.

Karine Amat (K)

Institut de Médecine et d'Epidémiologie Appliquées-Fondation Léon Mba, Hôpital Bichat-Claude Bernard, Paris, France.

Audrey Gabassi (A)

Service de Virologie, Hôpital Saint Louis, AP-HP, INSERM U944, Université de Paris, Paris, France.

Minh P Le (MP)

Service de Pharmacologie et Toxicologie, Hôpital Bichat, AP-HP, Infection Modelisation Antimicrobial Evolution, INSERM UMR1137, UF301, Université de Paris, Paris, France.

Robert Nzalakanda (R)

INSERM, Sorbonne Université, Institut Pierre Louis d'Epidémiologie et de Santé Publique, Paris, France.

Nadia Valin (N)

Service de Maladies Infectieuses et Tropicales, Hôpital Saint Antoine, AP-HP, Paris, France.

Roland Landman (R)

Service de Maladies Infectieuses, Hôpital Bichat, Infection Modelisation Antimicrobial Evolution, UMR1137, INSERM, Université de Paris, Paris, France.

Marie-Laure Chaix (ML)

Service de Virologie, Hôpital Saint Louis, AP-HP, INSERM U944, Université de Paris, Paris, France.

Constance Delaugerre (C)

Service de Virologie, Hôpital Saint Louis, AP-HP, INSERM U944, Université de Paris, Paris, France.

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Classifications MeSH