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Antiretroviral Treatment of HIV-2 Infection: Available Drugs, Resistance Pathways, and Promising New Compounds

dc.contributor.authorMoranguinho, Inês
dc.contributor.authorTaveira, Nuno
dc.contributor.authorBártolo, Inês
dc.date.accessioned2024-01-18T18:41:03Z
dc.date.available2024-01-18T18:41:03Z
dc.date.issued2023-03-21
dc.date.updated2023-10-25T13:04:56Z
dc.description© 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).pt_PT
dc.description.abstractCurrently, it is estimated that 1–2 million people worldwide are infected with HIV-2, accounting for 3–5% of the global burden of HIV. The course of HIV-2 infection is longer compared to HIV-1 infection, but without effective antiretroviral therapy (ART), a substantial proportion of infected patients will progress to AIDS and die. Antiretroviral drugs in clinical use were designed for HIV-1 and, unfortunately, some do not work as well, or do not work at all, for HIV-2. This is the case for non-nucleoside reverse transcriptase inhibitors (NNRTIs), the fusion inhibitor enfuvirtide (T-20), most protease inhibitors (PIs), the attachment inhibitor fostemsavir and most broadly neutralizing antibodies. Integrase inhibitors work well against HIV-2 and are included in first-line therapeutic regimens for HIV-2-infected patients. However, rapid emergence of drug resistance and cross-resistance within each drug class dramatically reduces second-line treatment options. New drugs are needed to treat infection with drug-resistant isolates. Here, we review the therapeutic armamentarium available to treat HIV-2-infected patients, as well as promising drugs in development. We also review HIV-2 drug resistance mutations and resistance pathways that develop in HIV-2-infected patients under treatment.pt_PT
dc.description.sponsorshipThis work was supported by Fundação para a Ciência e Tecnologia (FCT), Portugal, Aga Khan Development Network (AKDN)—Portugal Collaborative Research Network in Portuguese speaking countries in Africa (project 332821690). Inês Moranguinho was supported by PhD fellowship from Fundação para a Ciência e Tecnologia (FCT), Portugal (reference SFRH/BD/131062/2017) Inês Bártolo is supported by FCT through Norma Transitória—DL57/2016/CP1376/CT0012.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationMoranguinho I, Taveira N, Bártolo I. Antiretroviral treatment of hiv-2 infection: available drugs, resistance pathways, and promising new compounds. IJMS [Internet]. 21 de março de 2023;24(6):5905. Disponível em: https://www.mdpi.com/1422-0067/24/6/5905pt_PT
dc.identifier.doi10.3390/ijms24065905pt_PT
dc.identifier.slugcv-prod-3359445
dc.identifier.urihttp://hdl.handle.net/10451/61922
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherMDPIpt_PT
dc.relationGene therapy for HIV cure using RNA replicons.
dc.relation.publisherversionhttps://www.mdpi.com/1422-0067/24/6/5905pt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectHIV-2pt_PT
dc.subjectHIV-2 treatmentpt_PT
dc.subjectantiretroviral drugspt_PT
dc.subjectresistance mutationspt_PT
dc.subjectresistance pathwayspt_PT
dc.titleAntiretroviral Treatment of HIV-2 Infection: Available Drugs, Resistance Pathways, and Promising New Compoundspt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.awardTitleGene therapy for HIV cure using RNA replicons.
oaire.awardURIinfo:eu-repo/grantAgreement/FCT//SFRH%2FBD%2F131062%2F2017/PT
oaire.citation.issue6pt_PT
oaire.citation.startPage5905pt_PT
oaire.citation.titleInternational Journal of Molecular Sciencespt_PT
oaire.citation.volume24pt_PT
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.cv.cienciaid661E-F5CB-F85A | Inês Bártolo
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT
relation.isProjectOfPublication250af1fe-5815-4cce-8995-b19152bab737
relation.isProjectOfPublication.latestForDiscovery250af1fe-5815-4cce-8995-b19152bab737

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