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dc.contributor.authorHanevik, Kurten_US
dc.contributor.authorKristoffersen, Einar K.en_US
dc.contributor.authorSørnes, Steinaren_US
dc.contributor.authorMørch, Kristineen_US
dc.contributor.authorNæss, Halvoren_US
dc.contributor.authorRivenes, Ann Christinen_US
dc.contributor.authorBødtker, Jørnen_US
dc.contributor.authorHausken, Trygveen_US
dc.contributor.authorLangeland, Ninaen_US
dc.date.accessioned2013-05-14T10:32:22Z
dc.date.available2013-05-14T10:32:22Z
dc.date.issued2012-10-14eng
dc.PublishedBMC Infectious Diseases 2012, 12:258eng
dc.identifier.issn1471-2334
dc.identifier.urihttps://hdl.handle.net/1956/6605
dc.description.abstractBackground: A Giardia outbreak was associated with development of post-infectious functional gastrointestinal disorders (PI-FGID) and chronic fatigue syndrome (PI-CFS). Markers of immune dysfunction have given conflicting results in CFS and FGID patient populations. The aim of this study was to evaluate a wide selection of markers of immune dysfunction in these two co-occurring post-infectious syndromes. Methods: 48 patients, reporting chronic fatigue in a questionnaire study, were clinically evaluated five years after the outbreak and grouped according to Fukuda criteria for CFS (n=19) and idiopathic chronic fatigue (n=5) and Rome II criteria for FGIDs (n=54). 22 Giardia exposed non-fatigued individuals and 10 healthy unexposed individuals were recruited as controls. Peripheral blood lymphocyte subsets were analyzed by flow cytometry. Results: In peripheral blood we found significantly higher CD8 T-cell levels in PI-FGID, and significantly lower NK-cell levels in PI-CFS patients. Severity of abdominal and fatigue symptoms correlated negatively with NK-cell levels. A tendency towards lower T-cell CD26 expression in FGID was seen. Conclusion: Patients with PI-CFS and/or PI-FGID 5 years after Giardia lamblia infection showed alterations in NK-cell and CD8-cell populations suggesting a possible immunological abnormality in these conditions. We found no significant changes in other markers examined in this well-defined group of PI-CFS and PI-FGID elicited by a gastrointestinal infection. Controlling for co-morbid conditions is important in evaluation of CFS-biomarkers.en_US
dc.language.isoengeng
dc.publisherBioMed Centraleng
dc.relation.ispartof<a href="http://hdl.handle.net/1956/15491" target="_blank">Post-giardiasis functional gastrointestinal disorders and chronic fatigue syndrome – clinical symptoms, inflammation and immune responses</a>
dc.rightsAttribution CC BYeng
dc.rights.urihttp://creativecommons.org/licenses/by/2.0/eng
dc.subjectGiardia lambliaeng
dc.subjectFunctional gastrointestinal disordereng
dc.subjectChronic fatigue syndromeeng
dc.subjectIrritable bowel syndromeeng
dc.subjectNK cellseng
dc.subjectCD8 T-cellseng
dc.titleImmunophenotyping in post-giardiasis functional gastrointestinal disease and chronic fatigue syndromeen_US
dc.typePeer reviewed
dc.typeJournal article
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2012 Hanevik et al.; licensee BioMed Central Ltd.
dc.identifier.doihttps://doi.org/10.1186/1471-2334-12-258
dc.identifier.cristin997912
dc.source.journalBMC Infectious Diseases
dc.source.4012
dc.source.14258


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