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dc.contributor.authorBenito, José Miguel
dc.contributor.authorOrtiz, María C
dc.contributor.authorLeón, Agathe
dc.contributor.authorSarabia, Luis A
dc.contributor.authorLigos, Jose M. 
dc.contributor.authorMontoya, Maria 
dc.contributor.authorGarcia, Marcial
dc.contributor.authorRuiz-Mateos, Ezequiel
dc.contributor.authorPalacios, Rosario
dc.contributor.authorCabello, Alfonso
dc.contributor.authorRestrepo, Clara
dc.contributor.authorRodríguez, Carmen
dc.contributor.authorDel Romero, Jorge
dc.contributor.authorLeal, Manuel
dc.contributor.authorMuñoz-Fernández, María A
dc.contributor.authorAlcamí, José 
dc.contributor.authorGarcía, Felipe
dc.contributor.authorGórgolas, Miguel
dc.contributor.authorRallón, Norma
dc.contributor.authorECRIS
dc.date.accessioned2022-04-18T12:26:55Z
dc.date.available2022-04-18T12:26:55Z
dc.date.issued2018-02
dc.identifier.citationBMC Med. 2018 Feb 28;16(1):30.es_ES
dc.identifier.issn1741-7015es_ES
dc.identifier.otherhttp://hdl.handle.net/10668/12193
dc.identifier.urihttp://hdl.handle.net/20.500.12105/14105
dc.description.abstractBackground: Despite long-lasting HIV replication control, a significant proportion of elite controller (EC) patients may experience CD4 T-cell loss. Discovering perturbations in immunological parameters could help our understanding of the mechanisms that may be operating in those patients experiencing loss of immunological control. Methods: A case-control study was performed to evaluate if alterations in different T-cell homeostatic parameters can predict CD4 T-cell loss in ECs by comparing data from EC patients showing significant CD4 decline (cases) and EC patients showing stable CD4 counts (controls). The partial least-squares-class modeling (PLS-CM) statistical methodology was employed to discriminate between the two groups of patients, and as a predictive model. Results: Herein, we show that among T-cell homeostatic alterations, lower levels of naïve and recent thymic emigrant subsets of CD8 cells and higher levels of effector and senescent subsets of CD8 cells as well as higher levels of exhaustion of CD4 cells, measured prior to CD4 T-cell loss, predict the loss of immunological control. Conclusions: These data indicate that the parameters of T-cell homeostasis may identify those EC patients with a higher proclivity to CD4 T-cell loss. Our results may open new avenues for understanding the mechanisms underlying immunological progression despite HIV replication control, and eventually, for finding a functional cure through immune-based clinical trials.es_ES
dc.description.sponsorshipThis work has been partially funded by projects RD12/0017/0031, RD16/0025/0013, and SAF2015-66193-R as part of the Health Research and Development Strategy, State Plan for Scientific and Technical Research and Innovation (2008–2011 and 2013–2016) and cofinanced by the Institute of Health Carlos III (ISCIII), Sub-Directorate General for Research Assessment and Promotion and European Regional Development Fund. NR is a Miguel Servet investigator from the ISCIII (CP14/00198), Madrid, Spain. C Restrepo was funded by project RD12/0017/0031 and is currently funded by project RD16/0025/0013. M García is a predoctoral student co-funded by grant CP14/00198 and an Intramural Research Scholarship from Instituto de Investigación Sanitaria-Fundación Jiménez Díaz (IIS-FJD). The funders had no role in study design, data collection and analysis, the decision to publish, or the preparation of the manuscript.es_ES
dc.language.isoenges_ES
dc.publisherBioMed Central (BMC) es_ES
dc.relation66193es_ES
dc.type.hasVersionVoRes_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectCD4 T-cell losses_ES
dc.subjectCD8 exhaustiones_ES
dc.subjectClass modelinges_ES
dc.subjectElite controllerses_ES
dc.subjectT-cell homeostatic parameterses_ES
dc.subject.meshAdult es_ES
dc.subject.meshCD4-Positive T-Lymphocytes es_ES
dc.subject.meshCD8-Positive T-Lymphocytes es_ES
dc.subject.meshCase-Control Studies es_ES
dc.subject.meshDisease Progression es_ES
dc.subject.meshFemale es_ES
dc.subject.meshHIV Infections es_ES
dc.subject.meshHumans es_ES
dc.subject.meshMale es_ES
dc.subject.meshMiddle Aged es_ES
dc.subject.meshHomeostasis es_ES
dc.titleClass-modeling analysis reveals T-cell homeostasis disturbances involved in loss of immune control in elite controllerses_ES
dc.typeresearch articlees_ES
dc.rights.licenseAtribución 4.0 Internacional
dc.identifier.pubmedID29490663es_ES
dc.format.volume16es_ES
dc.format.number1es_ES
dc.format.page30es_ES
dc.identifier.doi10.1186/s12916-018-1026-6es_ES
dc.contributor.funderInstituto de Salud Carlos III es_ES
dc.contributor.funderUnión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF) es_ES
dc.contributor.funderInstituto de Investigación Sanitaria de la Fundación Jiménez Díaz es_ES
dc.description.peerreviewedes_ES
dc.identifier.e-issn1741-7015es_ES
dc.relation.publisherversionhttps://doi.org/10.1186/s12916-018-1026-6es_ES
dc.identifier.journalBMC Medicinees_ES
dc.repisalud.centroISCIII::Centro Nacional de Microbiologíaes_ES
dc.repisalud.institucionISCIIIes_ES
dc.rights.accessRightsopen accesses_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/MINECO//RD12%2F0017%2F0031/ES/SIDA/ es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/MINECO//RD16%2F0025%2F0013/ES/RED ESPAÑOLA DE INVESTIGACIÓN EN SIDA (RIS)/ es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/MINECO//SAF2015-66193-R/ES/UTILIZACION DE MEDICINA DE SISTEMAS PARA LA PREDICCION DE LA INMUNOGENICIDAD Y EFICACIA DE VACUNAS TERAPEUTICAS FRENTE A VIH/ es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/MINECO//CP14%2F00198/ES/CP14%2F00198/ es_ES


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Atribución 4.0 Internacional
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