Publication:
Biomarkers of innate immunity and immunological susceptibility to viral Infection in patients with alcoholic cirrhosis

dc.contributor.authorNavarro Noguera, Elena
dc.contributor.authorCollados Ros, Aurelia
dc.contributor.authorMiguel Bolarín, Jose
dc.contributor.authorMuro, Manuel
dc.contributor.authorLegaz Pérez, Isabel
dc.contributor.departmentCiencias Sociosanitarias
dc.date.accessioned2024-07-08T11:03:54Z
dc.date.available2024-07-08T11:03:54Z
dc.date.issued2024-02-01
dc.description© 2024 by the authors. This manuscript version is made available under the CC-BY 4.0 license http://creativecommons.org/licenses/by/4.0/ This document is the Published version of a Published Work that appeared in final form in Biomedicines. To access the final edited and published work see https://doi.org/10.3390/biomedicines12020336
dc.description.abstractBackground: The harmful effect of alcohol on the immune system may be due to both a direct action of the alcohol or its metabolites on immune cells as an indirect action modifying the different mechanisms of intercellular interaction. The interplay between stimulatory (aKIR) and inhibitory (iKIR) natural killer (NK) cell receptors and their corresponding human leukocyte antigen (HLA) ligands influences the outcome of virus infection. The aim was to analyze the influence of the KIR/HLA pair genetic profile in male alcoholic cirrhosis (AC) patients with and without viral infections to find susceptibility biomarkers that can help establish the risks and prevent viral infections. Methods: A total of 281 male AC patients were analyzed. The sociodemographic characteristics, viral hepatitis C (HCV), hepatitis B (HBV), and cytomegalovirus (CMV) infections were analyzed. Genomic DNA was extracted, and genetic the KIR/HLA profiles were investigated. A total of 6 KIR genes and their corresponding ligands (HLA-C) were analyzed. Patients were grouped into two groups: with and without associated viral infection. Results: A statistically significant increase in the combination of KIR2DL2+/C1C1 was observed in male AC patients with viral infection compared to those without viral infection (45.9% vs. 24.5%, p = 0.021). The analysis of KIR2DL3+/C1+ showed a high frequency comparing healthy controls and male AC patients without virus infection (85% vs. 76.4%; p = 0.026). The analysis of KIR2DL3+/C2C2 frequency showed a statistically significant increase comparing male AC patients without viral infection and healthy controls (23.6% vs. 15%; p = 0.026). Conclusions: The genetic KIR2DL2+/C2C2 profiles may play a significant role in determining the vulnerability of male AC patients to viral infections, providing valuable insights for future research and potential therapeutic interventions.es
dc.formatapplication/pdfes
dc.format.extent11es
dc.identifier.citationBiomedicines, 2024, Vol. 12 (2), 336
dc.identifier.doihttps://doi.org/10.3390/biomedicines12020336
dc.identifier.issnElectronic: 2227-9059
dc.identifier.urihttp://hdl.handle.net/10201/142922
dc.languageenges
dc.publisherMDPI
dc.relationOur work was possible thanks to support from Instituto de Salud Carlos III (ISCIII), Spanish Ministry of Economy and Competitiveness (grant number P19/01194), and co-funding from the European Union through the European Fund of Regional Development (FEDER) with the principle of “A manner to build Europe” and project of Fundacion Mutua Madrileña Grant Number AP183152023.es
dc.relation.publisherversionhttps://www.mdpi.com/2227-9059/12/2/336
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectAlcoholes
dc.subjectCirrhosises
dc.subjectHuman toxicologyes
dc.subjectKIR/HLA genes;es
dc.subjectNK cellses
dc.subjectViruses
dc.titleBiomarkers of innate immunity and immunological susceptibility to viral Infection in patients with alcoholic cirrhosises
dc.typeinfo:eu-repo/semantics/articlees
dspace.entity.typePublicationes
relation.isAuthorOfPublicationb83b4b59-2d61-40f0-9108-5c6a6d158295
relation.isAuthorOfPublication.latestForDiscoveryb83b4b59-2d61-40f0-9108-5c6a6d158295
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