dc.contributor.author |
Cseh, Áron |
|
dc.contributor.author |
Farkas, Márk Kristóf |
|
dc.contributor.author |
Derzbach, László |
|
dc.contributor.author |
Müller, Katalin Eszter |
|
dc.contributor.author |
Vásárhelyi, Barna |
|
dc.contributor.author |
Szalay, Balázs |
|
dc.contributor.author |
Farkas, Viktor |
|
dc.date.accessioned |
2015-06-11T14:05:18Z |
|
dc.date.available |
2015-06-11T14:05:18Z |
|
dc.date.issued |
2013 |
|
dc.identifier.citation |
pagination=1151-1155;
journalVolume=34;
journalIssueNumber=7;
journalTitle=NEUROLOGICAL SCIENCES; |
|
dc.identifier.uri |
http://repo.lib.semmelweis.hu//handle/123456789/1883 |
|
dc.description.abstract |
Aseptic inflammation due to activated immune cells has been implicated in the pathomechanism of migraine. We measured the prevalence of regulatory T cells (Tregs), along with that of CD4(+)/CD8(+) lymphocytes and their Th1/Th2 commitment in pediatric migraine. Children and adolescents suffering from migraine without aura, migraine with aura and hemiplegic migraine ictally (n = 53, 27, and 20, respectively), also interictally (n = 33) were recruited and compared to 24 healthy children. Our results indicated comparable prevalence of Tregs, CD4(+) and Th1/Th2 committed cells. CD8(+) prevalence was lower, and CD4(+)/CD8(+) ratio was higher in ictal phase irrespective of the subtype of migraine. No association between CD8(+) prevalence and gender, body weight, disease onset and attack duration in migraine subtypes was found. CD8(+) prevalence was normal in patients in interictal phase. These results suggest the absence of major systemic alteration of adaptive immunity in children and adolescents suffering from migraine; however, a transient decrease of CD8(+) prevalence during the ictal phase was detected irrespective of the subtype of migraine. |
|
dc.relation.ispartof |
urn:issn:1590-1874 |
|
dc.title |
Lymphocyte subsets in pediatric migraine |
|
dc.type |
Journal Article |
|
dc.date.updated |
2015-05-19T09:40:30Z |
|
dc.language.rfc3066 |
en |
|
dc.identifier.mtmt |
2372783 |
|
dc.identifier.pubmed |
23070628 |
|
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.department |
SE/AOK/I/Laboratóriumi Medicina Intézet |
|
dc.contributor.institution |
Semmelweis Egyetem |
|