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Spectrum of non-nucleoside reverse transcriptase inhibitor-associated drug resistance mutations in persons living with HIV-1 receiving rilpivirine

datacite.subject.fosCiências Médicas::Ciências da Saúde
datacite.subject.sdg03:Saúde de Qualidade
dc.contributor.authorNagarajan, Pavithra
dc.contributor.authorZhou, Jinru
dc.contributor.authorTeodoro, Giulia Di
dc.contributor.authorIncardona, Francesca
dc.contributor.authorSeguin-Devaux, Carole
dc.contributor.authorKaiser, Rolf
dc.contributor.authorAbecasis, Ana B.
dc.contributor.authorGomes, Perpétua
dc.contributor.authorTao, Kaiming
dc.contributor.authorZazzi, Maurizio
dc.contributor.authorShafer, Robert W.
dc.contributor.authoron behalf of the EuResist Network
dc.date.accessioned2026-04-23T13:51:53Z
dc.date.available2026-04-23T13:51:53Z
dc.date.issued2024-11
dc.description.abstractIntroduction: Few data are currently available on the nonnucleoside reverse transcriptase (RT) inhibitors (NNRTI) resistance mutations selected in persons living with HIV-1 (PLWH) who develop virological failure while receiving rilpivirine (RPV). Methods: We analyzed pooled HIV-1 RT genotypic data from 280 PLWH in the multicenter EuResist database and 115 PLWH in the Stanford HIV Drug Resistance Database (HIVDB) who received RPV as their only NNRTI. Results: Among the 395 PLWH receiving RPV, 180 (45.6%) had one or more NNRTI-associated DRMs. Overall, 44 NNRTI-associated DRMs were identified, including 26 that occurred in two or more PLWHs. Seven mutations had a prevalence ≥10% among the 180 PLWH with one or more NNRTI-associated DRM: E138K (32.2%), V90I (25.0%), K101E (17.8%), Y181C (17.2%), E138A (13.9%), H221Y (12.2%), and K103N (10.6%). Y181C was significantly more likely to co-occur with K101E, V179F, H221Y, and M230L. Ten novel non-polymorphic mutations at known NNRTI-associated mutation positions were also identified, usually in just one PLWH: L100F, V108A, T139I, P225S, M230V, Y232C, and T240A/I/M/S. Conclusions: Our analysis extends the spectrum of mutations emerging in PLWH receiving RPV. Additional phenotypic characterization of RPV-selected mutations is necessary to better understand their biological and possible clinical significance.eng
dc.identifier.citationNagarajan P, Zhou J, Di Teodoro G, Incardona F, Seguin-Devaux C, Kaiser R, Abecasis AB, Gomes P, Tao K, Zazzi M, et al. Spectrum of Non-Nucleoside Reverse Transcriptase Inhibitor-Associated Drug Resistance Mutations in Persons Living with HIV-1 Receiving Rilpivirine. Viruses. 2024; 16(11):1715. https://doi.org/10.3390/v16111715
dc.identifier.doi10.3390/v16111715
dc.identifier.issn1999-4915
dc.identifier.urihttp://hdl.handle.net/10400.26/62837
dc.language.isoeng
dc.peerreviewedyes
dc.publisherMDPI
dc.relation.hasversionhttps://doi.org/10.3390/v16111715
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectrilpivirine
dc.subjectHIV-1 drug resistance
dc.subjectnon-nucleoside reverse transcriptase inhibitors
dc.titleSpectrum of non-nucleoside reverse transcriptase inhibitor-associated drug resistance mutations in persons living with HIV-1 receiving rilpivirineeng
dc.typecontribution to journal
dspace.entity.typePublication
oaire.citation.issue11
oaire.citation.startPage1715
oaire.citation.titleViruses
oaire.citation.volume16
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85

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