Pharmacokinetic/pharmacodynamic investigation of raltegravir with or without lamivudine in the context of HIV-1 pre-exposure prophylaxis (PrEP).


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:
15 07 2021
Historique:
received: 17 01 2021
accepted: 05 04 2021
pubmed: 17 5 2021
medline: 11 8 2021
entrez: 16 5 2021
Statut: ppublish

Résumé

To characterize their potential use in pre-exposure prophylaxis (PrEP) we compared the pharmacokinetics of raltegravir and lamivudine in genital tissue against ex vivo tissue infection with HIV-1. Open-label trial of 36 HIV-negative females and males randomized to 7 days raltegravir 400 mg twice daily and 7 days raltegravir 400 mg+lamivudine 150 mg twice daily (after washout), or vice versa. Blood, saliva, rectal fluid, rectal tissue, vaginal fluid and vaginal tissue were sampled at baseline and on and off PrEP during a total of 12 days, for pharmacokinetics and antiviral activity via ex vivo HIV-1BaL challenge. Ex vivo infectivity was compared with baseline. The trial has been registered in https://clinicaltrials.gov/ with the identifier NCT03205566. Steady state for both drugs was reached by day 4. Dosing with raltegravir alone provided modest ex vivo HIV protection with higher drug levels in rectal tissue and vaginal tissue than in plasma on and off PrEP. Off PrEP, plasma and vaginal concentrations declined rapidly, while persisting in the rectum. On PrEP, the highest lamivudine concentrations were in the rectum, followed by vaginal tissue then plasma. Lamivudine washout was rapid in plasma, while persisting in the rectum and vagina. Raltegravir/lamivudine increased ex vivo protection on and off PrEP compared with raltegravir alone, reaching maximum protection at day 2 in rectal tissue and at day 8 in vaginal tissue. Raltegravir 400 mg+lamivudine 150 mg showed high levels of ex vivo HIV protection, associated with high drug concentrations persisting after discontinuation in vaginal and rectal compartments, supporting further investigation of these agents for PrEP.

Sections du résumé

BACKGROUND
To characterize their potential use in pre-exposure prophylaxis (PrEP) we compared the pharmacokinetics of raltegravir and lamivudine in genital tissue against ex vivo tissue infection with HIV-1.
METHODS
Open-label trial of 36 HIV-negative females and males randomized to 7 days raltegravir 400 mg twice daily and 7 days raltegravir 400 mg+lamivudine 150 mg twice daily (after washout), or vice versa. Blood, saliva, rectal fluid, rectal tissue, vaginal fluid and vaginal tissue were sampled at baseline and on and off PrEP during a total of 12 days, for pharmacokinetics and antiviral activity via ex vivo HIV-1BaL challenge. Ex vivo infectivity was compared with baseline. The trial has been registered in https://clinicaltrials.gov/ with the identifier NCT03205566.
RESULTS
Steady state for both drugs was reached by day 4. Dosing with raltegravir alone provided modest ex vivo HIV protection with higher drug levels in rectal tissue and vaginal tissue than in plasma on and off PrEP. Off PrEP, plasma and vaginal concentrations declined rapidly, while persisting in the rectum. On PrEP, the highest lamivudine concentrations were in the rectum, followed by vaginal tissue then plasma. Lamivudine washout was rapid in plasma, while persisting in the rectum and vagina. Raltegravir/lamivudine increased ex vivo protection on and off PrEP compared with raltegravir alone, reaching maximum protection at day 2 in rectal tissue and at day 8 in vaginal tissue.
CONCLUSIONS
Raltegravir 400 mg+lamivudine 150 mg showed high levels of ex vivo HIV protection, associated with high drug concentrations persisting after discontinuation in vaginal and rectal compartments, supporting further investigation of these agents for PrEP.

Identifiants

pubmed: 33993302
pii: 6276547
doi: 10.1093/jac/dkab136
pmc: PMC8325523
doi:

Substances chimiques

Anti-HIV Agents 0
Lamivudine 2T8Q726O95
Raltegravir Potassium 43Y000U234

Banques de données

ClinicalTrials.gov
['NCT03205566']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

2129-2136

Informations de copyright

© The Author(s) 2021. 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.

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Auteurs

Carolina Herrera (C)

Department of Medicine, Imperial College London, London, UK.

Julianne Lwanga (J)

Guys and St Thomas' NHS Foundation Trust and King's College London, London, UK.

Ming Lee (M)

Guys and St Thomas' NHS Foundation Trust and King's College London, London, UK.

Suna Mantori (S)

Guys and St Thomas' NHS Foundation Trust and King's College London, London, UK.

Alieu Amara (A)

Department of Pharmacology, University of Liverpool, Liverpool, UK.

Laura Else (L)

Department of Pharmacology, University of Liverpool, Liverpool, UK.

Sujan Dilly Penchala (SD)

Department of Pharmacology, University of Liverpool, Liverpool, UK.

Deirdre Egan (D)

Department of Pharmacology, University of Liverpool, Liverpool, UK.

Elizabeth Challenger (E)

Department of Pharmacology, University of Liverpool, Liverpool, UK.

Laura Dickinson (L)

Department of Pharmacology, University of Liverpool, Liverpool, UK.

Marta Boffito (M)

Chelsea and Westminster Hospital NHS Foundation Trust, London, UK.

Robin Shattock (R)

Department of Medicine, Imperial College London, London, UK.

Saye Khoo (S)

Department of Pharmacology, University of Liverpool, Liverpool, UK.

Julie Fox (J)

Guys and St Thomas' NHS Foundation Trust and King's College London, London, UK.

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