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dc.contributor.authorSantamaría Cadavid, María 
dc.contributor.authorRodriguez Castro, Emillio Francisco 
dc.contributor.authorRodríguez Yáñez, Manuel 
dc.contributor.authorArias Rivas, Susana 
dc.contributor.authorLópez Dequidt, Iria Alejandra 
dc.contributor.authorPérez Mato, María
dc.contributor.authorRodríguez Pérez, Manuel
dc.contributor.authorLópez Loureiro, Ignacio
dc.contributor.authorHervella ., Pablo
dc.contributor.authorCampos Pérez, Francisco 
dc.contributor.authorCastillo Sánchez, José 
dc.contributor.authorIglesias Rey, Ramón
dc.contributor.authorSobrino Moreiras, Tomas 
dc.date.accessioned2022-05-05T08:29:10Z
dc.date.available2022-05-05T08:29:10Z
dc.date.issued2020
dc.identifier.issn1471-2377
dc.identifier.otherhttps://www.ncbi.nlm.nih.gov/pubmed/32111174es
dc.identifier.urihttp://hdl.handle.net/20.500.11940/16694
dc.description.abstractBACKGROUND: Recent preclinical studies have shown that regulatory T cells (Treg) play a key role in the immune response after ischemic stroke (IS). However, the role of Treg in human acute IS has been poorly investigated. Our aim was to study the relationship between circulating Treg and outcome in human IS patients. METHODS: A total of 204 IS patients and 22 control subjects were recruited. The main study variable was good functional outcome at 3 months (modified Rankin scale </=2) considering infarct volume, Early Neurological Deterioration (END) and risk of infections as secondary variables. The percentage of circulating Treg was measured at admission, 48, 72 h and at day 7 after stroke onset. RESULTS: Circulating Treg levels were higher in IS patients compared to control subjects. Treg at 48 h were independently associated with good functional outcome (OR, 3.5; CI: 1.9-7.8) after adjusting by confounding factors. Patients with lower Treg at 48 h showed higher frequency of END and risk of infections. In addition, a negative correlation was found between circulating Treg at 48 h (r = - 0.414) and 72 h (r = - 0.418) and infarct volume. CONCLUSIONS: These findings suggest that Treg may participate in the recovery of IS patients. Therefore, Treg may be considered a potential therapeutic target in acute ischemic stroke.en
dc.rightsAtribución 4.0 Internacional
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.meshRisk Factors*
dc.subject.meshMiddle Aged*
dc.subject.meshHumans*
dc.subject.meshT-Lymphocytes*
dc.subject.meshInterleukin-10*
dc.subject.meshBrain Ischemia*
dc.subject.meshStroke*
dc.subject.meshAged*
dc.titleRegulatory T cells participate in the recovery of ischemic stroke patientsen
dc.typeJournal Articlees
dc.authorsophosSantamaria-Cadavid, M.;Rodriguez-Castro, E.;Rodriguez-Yanez, M.;Arias-Rivas, S.;Lopez-Dequidt, I.;Perez-Mato, M.;Rodriguez-Perez, M.;Lopez-Loureiro, I.;Hervella, P.;Campos, F.;Castillo, J.;Iglesias-Rey, R.;Sobrino, T.
dc.identifier.doi10.1186/s12883-020-01648-w
dc.identifier.pmid32111174
dc.identifier.sophos39962
dc.issue.number1es
dc.journal.titleBMC Neurologyes
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago de Compostela - Complexo Hospitalario Universitario de Santiago de Compostela::Neuroloxíaes
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS)es
dc.page.initial68es
dc.rights.accessRightsopenAccess
dc.subject.decsinterleucina-10*
dc.subject.decsanciano*
dc.subject.decsisquemia cerebral*
dc.subject.decsfactores de riesgo*
dc.subject.decslinfocitos T*
dc.subject.decsmediana edad*
dc.subject.decsaccidente cerebrovascular*
dc.subject.decshumanos*
dc.subject.keywordCHUSes
dc.subject.keywordIDISes
dc.typefidesArtículo Originales
dc.typesophosArtículo Originales
dc.volume.number20es


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Atribución 4.0 Internacional
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