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dc.contributor.authorPita-Martínez, Carlos 
dc.contributor.authorGoez-Sanz, Carmen
dc.contributor.authorVirseda-Berdices, Ana 
dc.contributor.authorGonzalez-Praetorius, Alejandro
dc.contributor.authorMazario-Martín, Esther
dc.contributor.authorRodriguez-Mesa, María
dc.contributor.authorAmigot-Sánchez, Rafael 
dc.contributor.authorMatías, Vanesa
dc.contributor.authorResino, Salvador 
dc.contributor.authorMartinez, Isidoro 
dc.date.accessioned2023-12-18T11:10:44Z
dc.date.available2023-12-18T11:10:44Z
dc.date.issued2024-01
dc.identifier.citationInt J Infect Dis. 2024 Jan:138:97-101.es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/16830
dc.description.abstractObjectives: We aimed to analyze whether the expression of inflammatory and antiviral genes in respiratory syncytial virus (RSV)-infected infants' peripheral blood is associated with bronchiolitis progression. Methods: We conducted a prospective study on 117 infants between 2015 and 2023. The expression levels of nine genes were quantified by quantitative polymerase chain reaction. Infants were classified according to their clinical evolution during hospital admission: (i) non-progression (n = 74), when the RSV bronchiolitis severity remained stable or improved; (ii) unfavorable progression (n = 43), when the RSV bronchiolitis severity increased. The association analysis was performed by logistic regression, adjusted by age, gender, prematurity, and RSV bronchiolitis severity in the emergency room. Results: Infants were 57.3% male, and the median age of the study population was 61 days. Thirty-five infants (30.7%) were admitted to the intensive care unit after hospital admission. Univariate logistic models showed that tumor necrosis factor (TNFα) and chemokine (C-C motif) ligand (CCL5) gene expression at baseline were inversely associated with unfavorable progression, which was confirmed by multivariate analyses: TNFα (adjusted odds ratio = 0.8 [95% confidence interval = 0.64-0.99], P-value = 0.038) and CCL5 (adjusted odds ratio = 0.76 [95% confidence interval = 0.62-0.93], P-value = 0.007). Conclusions: An inadequate immune response to RSV, characterized by reduced gene expression levels of CCL5 and TNFα in peripheral blood, was associated with an unfavorable progression of RSV bronchiolitis.es_ES
dc.description.sponsorshipThe study was funded by the CIBER -Consorcio Centro de Investigación Biomédica en Red- (CB 2021), Instituto de Salud Carlos III, Ministerio de Ciencia e Innovación and Unión Europea – NextGenerationEU (grant # CB21/13/00044 to SR)es_ES
dc.language.isoenges_ES
dc.publisherElsevier es_ES
dc.type.hasVersionVoRes_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectBronchiolitises_ES
dc.subjectCCL5es_ES
dc.subjectGene expressiones_ES
dc.subjectPeripheral bloodes_ES
dc.subjectRespiratory syncytial viruses_ES
dc.subjectTNFαes_ES
dc.titleLow peripheral blood chemokine (C-C motif) ligand 5 and tumor necrosis factor α gene expression is associated with unfavorable progression of respiratory syncytial virus bronchiolitis in infantses_ES
dc.typeresearch articlees_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.identifier.pubmedID38008352es_ES
dc.format.volume138es_ES
dc.format.page97-101es_ES
dc.identifier.doi10.1016/j.ijid.2023.11.024es_ES
dc.contributor.funderInstituto de Salud Carlos III es_ES
dc.contributor.funderUnión Europea. Comisión Europea. NextGenerationEU es_ES
dc.contributor.funderCentro de Investigación Biomédica en Red - CIBERINFEC (Enfermedades Infecciosas) es_ES
dc.contributor.funderMinisterio de Ciencia e Innovación (España) es_ES
dc.description.peerreviewedes_ES
dc.identifier.e-issn1878-3511es_ES
dc.relation.publisherversionhttps://doi.org/10.1016/j.ijid.2023.11.024es_ES
dc.identifier.journalInternational journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseaseses_ES
dc.repisalud.centroISCIII::Centro Nacional de Microbiologíaes_ES
dc.repisalud.institucionISCIIIes_ES
dc.rights.accessRightsopen accesses_ES
dc.relation.projectFISinfo:eu-repo/grantAgreement/ES/CB21/13/00044es_ES


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