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Giardia-specific cellular immune responses in post-giardiasis chronic fatigue syndrome

Hanevik, Kurt (författare)
Univ Bergen, Dept Clin Sci, Lab Bldg 8 Floor, N-5021 Bergen, Norway.;Haukeland Hosp, Ctr Trop Infect Dis, Bergen, Norway.
Kristoffersen, Einar (författare)
Univ Bergen, Dept Clin Sci, Lab Bldg 8 Floor, N-5021 Bergen, Norway.;Haukeland Hosp, Dept Immunol Transfus Med, Bergen, Norway.
Morch, Kristine (författare)
Univ Bergen, Dept Clin Sci, Lab Bldg 8 Floor, N-5021 Bergen, Norway.;Haukeland Hosp, Ctr Trop Infect Dis, Bergen, Norway.
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Rye, Kristin Paulsen (författare)
Univ Bergen, Dept Clin Sci, Lab Bldg 8 Floor, N-5021 Bergen, Norway.
Sornes, Steinar (författare)
Univ Bergen, Dept Clin Sci, Lab Bldg 8 Floor, N-5021 Bergen, Norway.
Svärd, Staffan (författare)
Uppsala universitet,Institutionen för cell- och molekylärbiologi
Bruserud, Oystein (författare)
Univ Bergen, Dept Clin Sci, Lab Bldg 8 Floor, N-5021 Bergen, Norway.
Langeland, Nina (författare)
Univ Bergen, Dept Clin Sci, Lab Bldg 8 Floor, N-5021 Bergen, Norway.;Haukeland Hosp, Ctr Trop Infect Dis, Bergen, Norway.
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Univ Bergen, Dept Clin Sci, Lab Bldg 8 Floor, N-5021 Bergen, Norway;Haukeland Hosp, Ctr Trop Infect Dis, Bergen, Norway. Univ Bergen, Dept Clin Sci, Lab Bldg 8 Floor, N-5021 Bergen, Norway.;Haukeland Hosp, Dept Immunol Transfus Med, Bergen, Norway. (creator_code:org_t)
2017-01-28
2017
Engelska.
Ingår i: BMC Immunology. - : BIOMED CENTRAL LTD. - 1471-2172. ; 18
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Background: The role of pathogen specific cellular immune responses against the eliciting pathogen in development of post-infectious chronic fatigue syndrome (PI-CFS) is not known and such studies are difficult to perform. The aim of this study was to evaluate specific anti-Giardia cellular immunity in cases that developed CFS after Giardia infection compared to cases that recovered well. Patients reporting chronic fatigue in a questionnaire study three years after a Giardia outbreak were clinically evaluated five years after the outbreak and grouped according to Fukuda criteria for CFS and idiopathic chronic fatigue. Giardia specific immune responses were evaluated in 39 of these patients by proliferation assay, T cell activation and cytokine release analysis. 20 Giardia exposed non-fatigued individuals and 10 healthy unexposed individuals were recruited as controls. Results: Patients were clinically classified into CFS (n = 15), idiopathic chronic fatigue (n = 5), fatigue from other causes (n = 9) and recovered from fatigue (n = 10). There were statistically significant antigen specific differences between these Giardia exposed groups and unexposed controls. However, we did not find differences between the Giardia exposed fatigue classification groups with regard to CD4 T cell activation, proliferation or cytokine levels in 6 days cultured PBMCs. Interestingly, sCD40L was increased in patients with PI-CFS and other persons with fatigue after Giardia infection compared to the non-fatigued group, and correlated well with fatigue levels at the time of sampling. Conclusion: Our data show antigen specific cellular immune responses in the groups previously exposed to Giardia and increased sCD40L in fatigued patients.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Immunologi inom det medicinska området (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Immunology in the medical area (hsv//eng)

Nyckelord

Giardia
T cell
Chronic fatigue syndrome
Antigen-specific
Immune response
sCD40L

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