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dc.contributor.authorMartín Escolano, Rubén
dc.contributor.authorVidal Alcántara, Erick Joan
dc.contributor.authorCrespo García, Javier 
dc.contributor.authorRyan, Pablo
dc.contributor.authorReal, Luis Miguel
dc.contributor.authorLazo-Álvarez, Juan Ignacio
dc.contributor.authorCabezas González, Joaquín
dc.contributor.authorMacías, Juan
dc.contributor.authorArias Loste, María Teresa 
dc.contributor.authorCuevas, Guillermo
dc.contributor.authorVirseda Berdices, Ana
dc.contributor.authorBriz, Verónica
dc.contributor.authorResino, Salvador
dc.contributor.authorJimenez Suosa, María Ángeles
dc.contributor.authorFernández Rodriguez, Amanda
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2024-01-25T18:35:55Z
dc.date.available2024-01-25T18:35:55Z
dc.date.issued2023
dc.identifier.issn1742-4933
dc.identifier.urihttps://hdl.handle.net/10902/31271
dc.description.abstractBackground: About 25% of patients with acute hepatitis C virus (HCV) infection show spontaneous clearance within the first six months of infection but may remain at risk of inflammaging, aging, and liver and non-liver disease complications. This study evaluated the differences in the plasma levels of immune checkpoints (ICs) and senescence-associated secretory phenotype (SASP) biomarkers between patients who had spontaneously eliminated HCV infection (SC group) and individuals without evidence of HCV infection (C group). Methods: We performed a multicenter retrospective study of 56 individuals: 32 in the SC and 24 in the C groups. ICs and SASP proteins were analyzed using a Luminex 200TM analyzer. The statistical analysis used Generalized Linear Models with gamma distribution (log-link) adjusted by significant variables and sex. Results: 13 ICs (BTLA, CD137(4-1BB), CD27, CD28, CD80, GITR, HVEM, IDO, LAG-3, PD-1, PD-L1, PD-L2, and TIM-3) and 13 SASP proteins (EGF, Eotaxin, IL-1alpha, IL-1RA, IL-8, IL-13, IL-18, IP-10, SDF-1alpha, HGF, beta-NGF, PLGF-1, and SCF) were significantly higher in SC group after approximately more than two years of HCV clearance. After stratifying by sex, differences remained significant for males, which showed higher levels for 13 ICs and 4 SASP proteins in SC. While only PD-L2 was significantly higher in SC women, and no differences in SASP were found. Conclusions: Higher plasma levels of different IC and SASP proteins were found in individuals after more than two years of HCV clearance, mainly in men. Alterations in these molecules might be associated with an increased risk of developing liver and non-hepatic diseaseses_ES
dc.description.sponsorshipEste estudio fue apoyado por subvenciones del Instituto de Salud Carlos III (ISCIII; subvención número CP14/0010) a AFR), Fundación Universidad Alfonso X el Sabio (FUAX) – Santander (subvención número 1.010.932 a AFR) y por PID2021–126781OB ‑I00 financiado por MCIN/AEI/10.13039/501100011033 y por “FEDER Una forma de hacer Europa”. El estudio también fue financiado por el CIBER ‑Consorcio Centro de Investigación Biomédica en Red‑ (CB 2021), Instituto de Salud Carlos III, Ministerio de Ciencia e Innovación y Unión Europea – NextGenerationEU (CB21/13/00044, CB21/13/00118 y GVC16/EHD/4). M.A.J.‑S. Es el investigador Miguel Servet apoyado y financiado por el ISCIII (números de subvención CP17CIII/00007). RME es el investigador Juan de la Cierva apoyado y financiado por el MICINN de España (FJC2020‑042865‑I).es_ES
dc.format.extent13 p.es_ES
dc.language.isoenges_ES
dc.publisherBioMed Centrales_ES
dc.rightsAttribution 4.0 Internationales_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourceImmunity & ageing : I & A, 2023, 20(1), 62es_ES
dc.subject.otherBiomarkerses_ES
dc.subject.otherHCVes_ES
dc.subject.otherImmune checkpoint proteinses_ES
dc.subject.otherSASP proteinses_ES
dc.subject.otherSpontaneous clearancees_ES
dc.titleImmunological and senescence biomarker profiles in patients after spontaneous clearance of hepatitis C virus: gender implications for long-term health riskes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1186/s12979-023-00387-z
dc.type.versionpublishedVersiones_ES


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Attribution 4.0 InternationalExcepto si se señala otra cosa, la licencia del ítem se describe como Attribution 4.0 International