Egyszerű nézet

dc.contributor.author Orbán, Csaba
dc.contributor.author Szabó, Dolóresz
dc.contributor.author Bajnok, Anna
dc.contributor.author Vásárhelyi, Barna
dc.contributor.author Tulassay, Tivadar
dc.contributor.author Arató, András
dc.contributor.author Veres, Gábor
dc.contributor.author Toldi, Gergely
dc.date.accessioned 2016-08-22T07:52:22Z
dc.date.available 2016-08-22T07:52:22Z
dc.date.issued 2016
dc.identifier 84979892926
dc.identifier.citation pagination=44966-44974; journalVolume=7; journalIssueNumber=29; journalTitle=ONCOTARGET;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/3639
dc.identifier.uri doi:10.18632/oncotarget.10036
dc.description.abstract OBJECTIVE: Crohn's disease is a chronic inflammation of the gastrointestinal tract with an abnormal immune phenotype. We investigated how intracellular calcium kinetics of Th1 and Th2 lymphocytes alter upon specific inhibition of Kv1.3 and IKCa1 channels in pediatric Crohn's disease. STUDY DESIGN: Blood was taken from 12 healthy and 29 Crohn's disease children. Of those, 6 were switched to infliximab and re-sampled after the 4th infliximab treatment. Intracellular calcium levels were monitored using flow cytometry in the presence or absence of specific inhibitors of Kv1.3 and IKCa1 potassium channels. RESULTS: In Crohn's disease treated with standard therapy, calcium response during activation was higher than normal in Th2 cells. This was normalized in vitro by inhibition of Kv1.3 or IKCa1 potassium channels. After the switch to infliximab, potassium channel function and expression in Th2 lymphocytes were comparable to those in Th1 cells. CONCLUSION: These results may indicate that potassium channels are potential immune modulatory targets in Crohn's disease.
dc.relation.ispartof urn:issn:1949-2553
dc.title Altered calcium influx of peripheral Th2 cells in pediatric Crohn’s disease: infliximab may normalize activation patterns
dc.type Journal Article
dc.date.updated 2016-08-19T08:01:18Z
dc.language.rfc3066 en
dc.identifier.mtmt 3084029
dc.identifier.pubmed 27329601
dc.contributor.department SE/AOK/K/I. Sz. Gyermekgyógyászati Klinika
dc.contributor.department SE/ETK2007/ALKEI/Dietetikai és Táplálkozástudományi Tanszék
dc.contributor.department SE/AOK/I/Laboratóriumi Medicina Intézet
dc.contributor.institution Semmelweis Egyetem


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