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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 2017-04-10T13:05:30Z
dc.date.available 2017-04-10T13:05:30Z
dc.date.issued 2017
dc.identifier.citation pagination=48-51; journalVolume=185; journalTitle=IMMUNOLOGY LETTERS;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/4214
dc.identifier.uri doi:10.1016/j.imlet.2017.03.009
dc.description.abstract AIM: Although Crohn's disease (CD) is an extensively investigated autoimmune condition, knowledge on early phase activation of lymphocytes, especially CD8+ Tc cells is scarce. Our aim was to investigate the calcium influx characteristics of CD8+ cells upon activation as well as the expression and function of Kv1.3 and IKCa1 lymphocyte potassium channels. METHODS: We took peripheral blood from 12 healthy controls, 23 CD children on conventional therapy and 6 severe CD children before and after infliximab therapy. Intracellular calcium levels were monitored in CD8+ lymphocytes using flow cytometry. RESULTS: In CD treated with standard therapy calcium response during activation was elevated. This was not affected by the inhibition of Kv1.3 or IKCa1 potassium channels. After the switch to infliximab potassium channel function and expression of CD8+ lymphocytes were comparable to healthy controls in severe CD. CONCLUSION: Calcium handling of CD8+ lymphocytes is altered in pediatric CD, which is normalized by infliximab therapy.
dc.relation.ispartof urn:issn:0165-2478
dc.title Altered activation of peripheral CD8+ T cells in pediatric Crohn's disease
dc.type Journal Article
dc.date.updated 2017-04-03T07:33:28Z
dc.language.rfc3066 en
dc.identifier.mtmt 3207422
dc.identifier.pubmed 28300604
dc.contributor.department SE/AOK/K/I. Sz. Gyermekgyógyászati Klinika
dc.contributor.department SE/AOK/K/ISZGYK/MTA-SE Gyermekgyógyászati és Nephrológiai Kutatócsoport
dc.contributor.institution Semmelweis Egyetem


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