Drug Interactions in Lenacapavir-Based Long-Acting Antiviral Combinations.


Journal

Viruses
ISSN: 1999-4915
Titre abrégé: Viruses
Pays: Switzerland
ID NLM: 101509722

Informations de publication

Date de publication:
31 05 2022
Historique:
received: 12 04 2022
revised: 25 05 2022
accepted: 27 05 2022
entrez: 24 6 2022
pubmed: 25 6 2022
medline: 28 6 2022
Statut: epublish

Résumé

Long-acting (LA) anti-HIV regimens show promise for increasing dosing intervals and consequently, improving the patients' quality of life. The first FDA-approved LA therapy is Cabenuva, which comprises rilpivirine (a non-nucleoside reverse transcriptase inhibitor) and cabotegravir (integrase strand transfer inhibitor). Novel promising LA anti-HIV agents such as lenacapavir (a capsid-targeting antiviral) and islatravir (EFdA, a nucleoside reverse transcriptase translocation inhibitor) need to be explored as combination therapies. Therefore, we sought to determine whether combination of lenacapavir with islatravir, rilpivirine, or cabotegravir displayed synergy, additivity, or antagonism. We performed dose-response matrices of these drug combinations in an HIV-1 reporter cell line and subsequently analyzed the data with SynergyFinder Plus, which employs four major drug interaction models: highest single agent, Bliss independence, Loewe additivity, and zero interaction potency. Most of these models predict additive inhibition by the studied drug combinations This work highlights the importance of effective drug combinations in LA-regimens.

Identifiants

pubmed: 35746673
pii: v14061202
doi: 10.3390/v14061202
pmc: PMC9229705
pii:
doi:

Substances chimiques

Anti-HIV Agents 0
Drug Combinations 0
Reverse Transcriptase Inhibitors 0
cabotegravir, rilpivirine drug combination 0
Rilpivirine FI96A8X663

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIAID NIH HHS
ID : F31 AI155158-01A1
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM008367
Pays : United States
Organisme : NIAID NIH HHS
ID : F31 AI155158
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI120860
Pays : United States
Organisme : NIAID NIH HHS
ID : U54 AI150472
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI148382
Pays : United States
Organisme : NIAID NIH HHS
ID : R37 AI076119
Pays : United States

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Auteurs

Maria E Cilento (ME)

Laboratory of Biochemical Pharmacology, Department of Pediatrics, Emory University School of Medicine, Children's Healthcare of Atlanta, Atlanta, GA 30307, USA.

Yee Tsuey Ong (YT)

Laboratory of Biochemical Pharmacology, Department of Pediatrics, Emory University School of Medicine, Children's Healthcare of Atlanta, Atlanta, GA 30307, USA.

Philip R Tedbury (PR)

Laboratory of Biochemical Pharmacology, Department of Pediatrics, Emory University School of Medicine, Children's Healthcare of Atlanta, Atlanta, GA 30307, USA.

Stefan G Sarafianos (SG)

Laboratory of Biochemical Pharmacology, Department of Pediatrics, Emory University School of Medicine, Children's Healthcare of Atlanta, Atlanta, GA 30307, USA.

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Classifications MeSH