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dc.contributor.authorNavarrete Muñoz, María
dc.contributor.authorRamos, Ricardo
dc.contributor.authorHolguín, África
dc.contributor.authorCabello Ubeda, Alfonso 
dc.contributor.authorGórgolas Hernández-Mora, Miguel 
dc.contributor.authorBenito, José M.
dc.contributor.authorRallón, Norma
dc.date.accessioned2023-05-25T07:01:30Z
dc.date.available2023-05-25T07:01:30Z
dc.date.issued2022-10-03
dc.identifier.citationVirulence 13.1 (2022): 1713-1719es_ES
dc.identifier.issn2150-5594 (print)es_ES
dc.identifier.issn2150-5608 (online)es_ES
dc.identifier.urihttp://hdl.handle.net/10486/707279
dc.descriptionData that support the findings of this study are available from the corresponding author upon reasonable requestes_ES
dc.description.abstractAccumulation of mutations in epitopes of cytolytic-T-lymphocytes immune response (CTL) in HIV-reservoir seems to be one of the reasons for shock-and-kill strategy failure. Ten non-controller patients on successful cART (TX) and seven elite controllers (EC) were included. HIV-Gag gene from purified resting memory CD4+ T-cells was sequenced by Next-Generation-Sequencing. HLA class-I alleles were typed to predict optimal HIV-Gag CTL epitopes. For each subject, the frequency of mutated epitopes in the HIV-Gag gene, the proportion of them considered as CTL-escape variants as well as their effect on antigen recognition by HLA were assessed. The proportion (%) of mutated HIV-Gag CTL epitopes in the reservoir was high and similar in EC and TX (86%[50–100] and 57%[48–82] respectively, p=0.315). Many of them were predicted to negatively impact antigen recognition. Moreover, the proportion of mutated epitopes considered to be CTL-escape variants was also similar in TX and EC (77%[49–92] vs. 50%[33–75] respectively, p=0.117). Thus, the most relevant finding of our study was the high and similar proportions of HIV-Gag CTL-escape mutations in the reservoir of both HIV-noncontroller patients with cART (TX) and patients with spontaneous HIV-control (EC). Our findings suggest that escape mutations of CTL-response may be another obstacle to eliminate the HIV reservoir and constitute a proof of concept that challenges HIV cure strategies focused on the reactivation of reservoirs. Due to the small sample size that could impact the robustness of the study, further studies with larger cohorts of elite controller patients are needed to confirm these results.es_ES
dc.format.extent8 pag.es_ES
dc.format.mimetypeapplication/pdfes_ES
dc.language.isoenges_ES
dc.publisherTaylor & Francises_ES
dc.relation.ispartofVirulencees_ES
dc.rights© 2022 The Author(s)es_ES
dc.subject.otherCTL responsees_ES
dc.subject.otherelite controllerses_ES
dc.subject.otherHIV reservoires_ES
dc.subject.otherHIV-Gag proviral DNAes_ES
dc.subject.othernext generation sequencing (NGS)es_ES
dc.subject.otherresting memory CD4+ T-cellses_ES
dc.titleHigh frequency of CD8 escape mutations in elite controllers as new obstacle for HIV curees_ES
dc.typearticlees_ES
dc.subject.ecienciaMedicinaes_ES
dc.identifier.doi10.1080/21505594.2022.2129353es_ES
dc.identifier.publicationfirstpage1713es_ES
dc.identifier.publicationissue1es_ES
dc.identifier.publicationlastpage1719es_ES
dc.identifier.publicationvolumeVirulencees_ES
dc.type.versioninfo:eu-repo/semantics/publishedVersiones_ES
dc.rights.ccReconocimientoes_ES
dc.rights.accessRightsopenAccesses_ES
dc.facultadUAMFacultad de Medicina
dc.institutoUAMInstituto de Investigación Sanitaria Fundación Jiménez Díaz (ISS-FJD)es_ES
dc.institutoUAMInstituto Ramón y Cajal de Investigación Sanitaria (IRYCIS)es_ES


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