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HIV latency reversal agents: A potential path for functional cure?

dc.contributor.authorLopes, Juliana Romano [UNESP]
dc.contributor.authorChiba, Diego Eidy [UNESP]
dc.contributor.authorDos Santos, Jean Leandro [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2021-06-25T10:21:39Z
dc.date.available2021-06-25T10:21:39Z
dc.date.issued2021-03-05
dc.description.abstractDespite the advances in Human Immunodeficiency Virus (HIV) treatment, the cure for all HIV patients still poses a major challenge, which needs to be surpassed in the coming years. Among the strategies pursuing this aim, the ‘kick-and-kill’ approach, which involves the reactivation and elimination of a latent HIV reservoir that resides in some CD4+ T cells, appears promising. The first step of this approach requires the use of latency reversal agents (LRAs) that induce the reactivation of the latent virus. Although several classes of LRAs have been reported so far, some limitations of these compounds still need to be overcome before their clinical use. The complete exhaustion of the reservoir of latent virus will contribute to promote the second step of this approach, facilitating the elimination of the reactivated HIV. Therefore, potent, safe, and non-toxic LRAs are necessary to promote efficient elimination of the HIV-1 virus from its reservoir. In this review article, we focus on the promising LRAs that have been described in the literature over the past few years, highlighting the advantages and disadvantages of their use in the ‘kick and kill’ approach, thus opening a new avenue in the development of a potential cure.en
dc.description.affiliationSão Paulo State University (UNESP) School of Pharmaceutical Sciences
dc.description.affiliationInstitute of Chemistry São Paulo State University (UNESP)
dc.description.affiliationUnespSão Paulo State University (UNESP) School of Pharmaceutical Sciences
dc.description.affiliationUnespInstitute of Chemistry São Paulo State University (UNESP)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdCAPES: 001
dc.description.sponsorshipIdFAPESP: 2018/11079-0
dc.identifierhttp://dx.doi.org/10.1016/j.ejmech.2021.113213
dc.identifier.citationEuropean Journal of Medicinal Chemistry, v. 213.
dc.identifier.doi10.1016/j.ejmech.2021.113213
dc.identifier.issn1768-3254
dc.identifier.issn0223-5234
dc.identifier.scopus2-s2.0-85100116725
dc.identifier.urihttp://hdl.handle.net/11449/205808
dc.language.isoeng
dc.relation.ispartofEuropean Journal of Medicinal Chemistry
dc.sourceScopus
dc.subjectBromodomain inhibitors
dc.subjectHistone deacetylase inhibitors
dc.subjectHIV
dc.subjectKick and kill approach
dc.subjectLatency reversal agents
dc.subjectProtein kinase C agonists
dc.titleHIV latency reversal agents: A potential path for functional cure?en
dc.typeResenhapt
dspace.entity.typePublication
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relation.isOrgUnitOfPublicationbc74a1ce-4c4c-4dad-8378-83962d76c4fd
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.author.orcid0000-0003-2844-6402[2]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt

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