Drug Interactions in Lenacapavir-Based Long-Acting Antiviral Combinations.
EFdA
islatravir
long-acting regimens
synergy
Journal
Viruses
ISSN: 1999-4915
Titre abrégé: Viruses
Pays: Switzerland
ID NLM: 101509722
Informations de publication
Date de publication:
31 05 2022
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
Références
Curr Opin Infect Dis. 2021 Feb 1;34(1):8-15
pubmed: 33337617
Curr Opin HIV AIDS. 2018 Jul;13(4):294-299
pubmed: 29697468
J Virol. 2008 Dec;82(24):12585-8
pubmed: 18842727
Genomics Proteomics Bioinformatics. 2022 Jan 24;:
pubmed: 35085776
Infect Disord Drug Targets. 2018;18(1):15-22
pubmed: 28474549
Arzneimittelforschung. 1953 Jun;3(6):285-90
pubmed: 13081480
PLoS Comput Biol. 2019 May 20;15(5):e1006752
pubmed: 31107860
Drugs. 2020 Jun;80(9):915-922
pubmed: 32495274
Proc Natl Acad Sci U S A. 1993 Sep 15;90(18):8392-6
pubmed: 7690960
JAMA. 2018 Mar 27;319(12):1261-1268
pubmed: 29584848
Pharmacol Rev. 1989 Jun;41(2):93-141
pubmed: 2692037
Comput Struct Biotechnol J. 2015 Sep 25;13:504-13
pubmed: 26949479