Publication:
Elite controllers long-term non progressors present improved survival and slower disease progression

dc.contributor.authorCapa, Laura
dc.contributor.authorAyala-Suarez, Ruben
dc.contributor.authorde la Torre-Tarazona, Humberto Erick
dc.contributor.authorGonzález-García, Juan
dc.contributor.authorDel Romero, Jorge
dc.contributor.authorAlcamí, José
dc.contributor.authorDíez-Fuertes, Francisco
dc.contributor.funderCentro de Investigación Biomédica en Red - CIBERINFEC (Enfermedades Infecciosas)es_ES
dc.contributor.funderRed de Investigación Cooperativa en Investigación en Sida (España)es_ES
dc.contributor.funderInstituto de Salud Carlos IIIes_ES
dc.contributor.funderPlan Nacional de I+D+i (España)es_ES
dc.contributor.funderUnión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF)es_ES
dc.date.accessioned2023-01-25T14:31:44Z
dc.date.available2023-01-25T14:31:44Z
dc.date.issued2022-09-29
dc.description.abstractDifferent phenotypes exhibiting no evidences of disease progression have been described in ART-naïve HIV-1 positive individuals. Long-term non progressors (LTNP) and elite controllers (EC) are low frequent examples of immunological and virological control in HIV-1 positive subjects, respectively. The combination of both phenotypes is even less frequent and studied despite being considered as models of HIV-1 functional cure. A multicenter, prospective study in retrospect including clinical and epidemiological data collected from 313 LTNP of 21 Spanish hospitals was carried out. LTNPs maintaining CD4+ T cell counts over 500 cells/µl and viral loads (VL) under 10,000 copies/mL for at least 10 years in the absence of antiretroviral therapy were followed for a median of 20.8 years (IQR = 15.6-25.5). A 52.1% were considered EC (undetectable VL) and LTNP (EC-LTNP) and a total of 171 (54.8%) and 42 (13.5%) out of the 313 participants maintained LTNP status for at least 20 and 30 years, respectively. EC-LTNP showed lower CD4+ T cell count loss (9.9 vs 24.2 cells/µl/year), higher CD4/CD8 ratio (0.01 vs - 0.09 in ratio), and lesser VL increase (no increase vs 197.2 copies/mL/year) compared with LTNPs with detectable VL (vLTNP). Survival probabilities for all-cause mortality at 30 years from HIV + diagnosis were 0.90 for EC-LTNP and 0.70 for vLTNP (p = 2.0 × 10-3), and EC-LTNP phenotype was the only factor associated with better survival in multivariate analyses (HR = 0.28; 95% CI 0.10-0.79). The probability to preserve LTNP status at 30 years was 0.51 for EC-LTNP and 0.18 for vLTNP (p < 2.2 × 10-16). Risk factors associated to the loss of LTNP status was: higher age at diagnosis and the increase of VL, whereas the increase of CD4+ T cell counts and CD4/CD8 ratio, the initial EC-LTNP phenotype and HCV coinfection were protective factors. EC-LTNP phenotype was associated with improved survival and slower disease progression compared with other phenotypes of LTNP. EC-LTNP individuals represent one of the most favorable phenotypes of immune activation against HIV-1 found in nature and, therefore, are strong candidates to be considered a model of functional cure of HIV-1 infection.es_ES
dc.description.peerreviewedes_ES
dc.description.sponsorshipThis study has been conducted within the Infectious Diseases Networking Biomedical Research Centre (CIBER INFEC) and the Spanish AIDS Research Network (RIS), the latter being funded by the Instituto de Salud Carlos III (Project RD16CIII/0002/0001, Plan Estatal de I+D+I 2013–2016) and co-fnanced by the European Regional Development Fund (ERDF) “A way to build Europe”. Te study was funded by the Instituto de Salud Carlos III (Project PI19CIII/00004).es_ES
dc.format.number1es_ES
dc.format.page16356es_ES
dc.format.volume12es_ES
dc.identifier.citationSci Rep. 2022 Sep 29;12(1):16356.es_ES
dc.identifier.doi10.1038/s41598-022-19970-3es_ES
dc.identifier.e-issn2045-2322es_ES
dc.identifier.journalScientific reportses_ES
dc.identifier.pubmedID36175445es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/15433
dc.language.isoenges_ES
dc.publisherNature Publishing Groupes_ES
dc.relation.projectFISinfo:eu-repo/grantAgreement/ES/RD16CIII/0002/0001es_ES
dc.relation.projectFISinfo:fis/Instituto de Salud Carlos III/Programa Estatal de Generación de Conocimiento y Fortalecimiento del Sistema Español de I+D+I/Subprograma Estatal de Generación de Conocimiento/PI19-ISCIII Modalidad Proyectos de Investigacion en Salud Intramurales. (2019)/PI19CIII/00004es_ES
dc.relation.publisherversionhttps://doi.org/10.1038/s41598-022-19970-3es_ES
dc.repisalud.centroISCIII::Centro Nacional de Microbiologíaes_ES
dc.repisalud.institucionISCIIIes_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.meshHIV Seropositivityes_ES
dc.subject.meshHIV-1es_ES
dc.subject.meshCD4 Lymphocyte Countes_ES
dc.subject.meshDisease Progressiones_ES
dc.subject.meshElite Controllerses_ES
dc.subject.meshHumanses_ES
dc.subject.meshProspective Studieses_ES
dc.subject.meshViral Loades_ES
dc.titleElite controllers long-term non progressors present improved survival and slower disease progressiones_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
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relation.isAuthorOfPublication596e4147-6554-4a46-b44f-ee859e2a2053
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relation.isAuthorOfPublication05199c38-bb50-4a79-bb3b-96dce9769920
relation.isAuthorOfPublication.latestForDiscovery353e66d9-30cb-4602-b54b-2c9d5a0e7ec8

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