Immunophenotyping in post-giardiasis functional gastrointestinal disease and chronic fatigue syndrome

<p>Abstract</p> <p>Background</p> <p>A <it>Giardia</it> 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 re...

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Main Authors: Hanevik Kurt, Kristoffersen Einar K, Sørnes Steinar, Mørch Kristine, Næss Halvor, Rivenes Ann C, Bødtker Jørn E, Hausken Trygve, Langeland Nina
Format: Article
Language:English
Published: BMC 2012-10-01
Series:BMC Infectious Diseases
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Online Access:http://www.biomedcentral.com/1471-2334/12/258
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Summary:<p>Abstract</p> <p>Background</p> <p>A <it>Giardia</it> 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.</p> <p>Methods</p> <p>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 <it>Giardia</it> exposed non-fatigued individuals and 10 healthy unexposed individuals were recruited as controls. Peripheral blood lymphocyte subsets were analyzed by flow cytometry.</p> <p>Results</p> <p>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.</p> <p>Conclusion</p> <p>Patients with PI-CFS and/or PI-FGID 5 years after <it>Giardia lamblia</it> 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.</p>
ISSN:1471-2334