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dc.contributor.authorLara-Aguilar, Violeta 
dc.contributor.authorCrespo-Bermejo, Celia 
dc.contributor.authorLlamas-Adán, Manuel 
dc.contributor.authorGrande-García, Sergio 
dc.contributor.authorCortijo-Alfonso, María Engracia 
dc.contributor.authorMartín-Carbonero, Luz
dc.contributor.authorDomínguez, Lourdes
dc.contributor.authorRyan, Pablo
dc.contributor.authorde Los Santos, Ignacio
dc.contributor.authorBartolomé-Sánchez, Sofía 
dc.contributor.authorValle-Millares, Daniel 
dc.contributor.authorJimenez-Sousa, Maria Angeles 
dc.contributor.authorBriz, Veronica 
dc.contributor.authorFernandez-Rodriguez, Amanda 
dc.contributor.authorMultidisciplHIV/Hepatitis Viral Coinfection Group (COVIHEP)
dc.date.accessioned2023-08-24T09:00:45Z
dc.date.available2023-08-24T09:00:45Z
dc.date.issued2023-07
dc.identifier.citationJ Med Virol. 2023 Jul;95(7):e28955.es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/16335
dc.description.abstractCoinfection with hepatitis C virus (HCV) and human immunodeficiency virus (HIV) increases immune activation, inflammation, and oxidative stress that could lead to premature senescence. Different HCV infections, either acute or chronic infection, could lead to distinct premature cellular senescence in people living with HIV (PLWHIV). Observational study in 116 PLWHIV under antiretroviral treatment with different HCV status: (i) n = 45 chronically infected with HCV (CHC); (ii) n = 36 individuals who spontaneously clarify HCV (SC); (iii) n = 35 HIV controls. Oxidative stress biomarkers were analyzed at lipid, DNA, protein, and nitrates levels, as well as antioxidant capacity and glutathione reductase enzyme. Replicative senescence was evaluated by relative telomere length (RTL) measurement. Additionally, 26 markers of Senescence-Associated Secretory Phenotype (SASP) were analyzed by multiplex immunoassays (Luminex xMAP technology). Differences were evaluated by generalized linear model (GLMs) adjusted by most significant covariates. The SC group had a senescence signature similar to the HIV control group and slightly lower SASP levels. However, significant differences were observed with respect to the CHC group, where an increase in the nitrate concentration [adjusted arithmetic mean ratio, aAMR = 1.73 (1.27-2.35), p < 0.001, q = 0.009] and the secretion of 13 SASP-associated factors [granulocyte macrophage colony-stimulating factor (GM-CSF), interferon-β, interleukin (IL)-1β, IL-2, IL-8, IL-13, tumor necrosis factor (TNF)-α, IL-1α, IL-1RA, IL-7, IL-15, C-X-C motif chemokine ligand 10 (IP-10), stem cell factor (SCF); q < 0.1)] was detected. The CHC group also showed higher values of IL-1α, IP-10, and placental growth factor 1 (PIGF-1) than HIV controls. The SC group showed a slightly lower senescence profile than the HIV group, which could indicate a more efficient control of viral-induced senescence due to their immune strengths. Chronic HCV infection in PLWHIV led to an increase in nitrate and elevated SASP biomarkers favoring the establishment of viral persistence.es_ES
dc.description.sponsorshipThis study was supported by grants from Ministerio de Ciencia e Innovación (grant number PID2021‐126781OB‐I00 to A. F. R. and V. B.) funded by MCIN/AEI/10.13039/501100011033 by “ERDF A way of making Europe,” Instituto de Salud Carlos III (PI15CIII/00031 and PI18CIII/00020 to V. B. and A. F. R.), Fundación Universidad Alfonso X el Sabio (FUAX)—Santander (grant number 1.010.932 to A. F. R.). The study was also supported by the Centro de Investigación Biomédica en Red (CIBER) en Enfermedades Infecciosas (CB21/13/00044 and CB21/13/00107).es_ES
dc.language.isoenges_ES
dc.publisherWiley es_ES
dc.type.hasVersionVoRes_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectHCV/HIVes_ES
dc.subjectSASPes_ES
dc.subjectOxidative stresses_ES
dc.subjectSenescencees_ES
dc.subjectSpontaneous clearancees_ES
dc.subjectTelomerees_ES
dc.subject.meshHIV Infections es_ES
dc.subject.meshHepatitis C es_ES
dc.subject.meshCoinfection es_ES
dc.subject.meshHumans es_ES
dc.subject.meshFemale es_ES
dc.subject.meshHIV es_ES
dc.subject.meshHepacivirus es_ES
dc.subject.meshChemokine CXCL10 es_ES
dc.subject.meshNitrates es_ES
dc.subject.meshPlacenta Growth Factor es_ES
dc.subject.meshBiomarkers es_ES
dc.subject.meshTumor Necrosis Factor-alpha es_ES
dc.titleHCV spontaneous clearers showed low senescence profile in people living with HIV under long ARTes_ES
dc.typeresearch articlees_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.identifier.pubmedID37465865es_ES
dc.format.volume95es_ES
dc.format.number7es_ES
dc.format.pagee28955es_ES
dc.identifier.doi10.1002/jmv.28955es_ES
dc.contributor.funderMinisterio de Ciencia e Innovación (España) es_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.funderFundación Universidad Alfonso X el Sabio es_ES
dc.contributor.funderFundación Banco Santander es_ES
dc.contributor.funderCentro de Investigación Biomédica en Red - CIBERINFEC (Enfermedades Infecciosas) es_ES
dc.contributor.funderAgencia Estatal de Investigación (España) es_ES
dc.description.peerreviewedes_ES
dc.identifier.e-issn1096-9071es_ES
dc.relation.publisherversionhttps://doi.org/10.1002/jmv.28955es_ES
dc.identifier.journalJournal of medical virologyes_ES
dc.repisalud.centroISCIII::Centro Nacional de Microbiologíaes_ES
dc.repisalud.institucionISCIIIes_ES
dc.rights.accessRightsopen accesses_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/PID2021‐126781OB‐I00es_ES
dc.relation.projectFISinfo:eu-repo/grantAgreement/ES/PI15CIII/00031es_ES
dc.relation.projectFISinfo:fis/Instituto de Salud Carlos III/Programa Estatal de Fomento de la Investigación Científica y Técnica de Excelencia/Subprograma Estatal de Generación de Conocimiento/PI18-ISCIII Modalidad Proyectos de Investigacion en Salud Intramurales. (2018)/PI18CIII/00020es_ES
dc.relation.projectFISinfo:eu-repo/grantAgreement/ES/CB21/13/00044es_ES
dc.relation.projectFISinfo:eu-repo/grantAgreement/ES/CB21/13/00107es_ES


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