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

BACKGROUND: 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 eval...

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Autores principales: Hanevik, Kurt, Kristoffersen, Einar K, Sørnes, Steinar, Mørch, Kristine, Næss, Halvor, Rivenes, Ann C, Bødtker, Jørn E, Hausken, Trygve, Langeland, Nina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3553045/
https://www.ncbi.nlm.nih.gov/pubmed/23061432
http://dx.doi.org/10.1186/1471-2334-12-258
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author Hanevik, Kurt
Kristoffersen, Einar K
Sørnes, Steinar
Mørch, Kristine
Næss, Halvor
Rivenes, Ann C
Bødtker, Jørn E
Hausken, Trygve
Langeland, Nina
author_facet Hanevik, Kurt
Kristoffersen, Einar K
Sørnes, Steinar
Mørch, Kristine
Næss, Halvor
Rivenes, Ann C
Bødtker, Jørn E
Hausken, Trygve
Langeland, Nina
author_sort Hanevik, Kurt
collection PubMed
description BACKGROUND: 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.
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spelling pubmed-35530452013-01-28 Immunophenotyping in post-giardiasis functional gastrointestinal disease and chronic fatigue syndrome Hanevik, Kurt Kristoffersen, Einar K Sørnes, Steinar Mørch, Kristine Næss, Halvor Rivenes, Ann C Bødtker, Jørn E Hausken, Trygve Langeland, Nina BMC Infect Dis Research Article BACKGROUND: 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. BioMed Central 2012-10-14 /pmc/articles/PMC3553045/ /pubmed/23061432 http://dx.doi.org/10.1186/1471-2334-12-258 Text en Copyright ©2012 Hanevik et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Hanevik, Kurt
Kristoffersen, Einar K
Sørnes, Steinar
Mørch, Kristine
Næss, Halvor
Rivenes, Ann C
Bødtker, Jørn E
Hausken, Trygve
Langeland, Nina
Immunophenotyping in post-giardiasis functional gastrointestinal disease and chronic fatigue syndrome
title Immunophenotyping in post-giardiasis functional gastrointestinal disease and chronic fatigue syndrome
title_full Immunophenotyping in post-giardiasis functional gastrointestinal disease and chronic fatigue syndrome
title_fullStr Immunophenotyping in post-giardiasis functional gastrointestinal disease and chronic fatigue syndrome
title_full_unstemmed Immunophenotyping in post-giardiasis functional gastrointestinal disease and chronic fatigue syndrome
title_short Immunophenotyping in post-giardiasis functional gastrointestinal disease and chronic fatigue syndrome
title_sort immunophenotyping in post-giardiasis functional gastrointestinal disease and chronic fatigue syndrome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3553045/
https://www.ncbi.nlm.nih.gov/pubmed/23061432
http://dx.doi.org/10.1186/1471-2334-12-258
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