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J Infect. 2019 Jan 23. pii: S0163-4453(19)30027-1. doi: 10.1016/j.jinf.2019.01.006. [Epub ahead of print]
Cytokine profiles in patients with Q fever fatigue syndrome.
Raijmakers RPH1, Koeken V2, Jansen AFM3, Keijmel SP4, Roerink ME5, Joosten LAB6, Netea MG7, van der Meer JWM8, Bleeker-Rovers CP9.
Author information
Abstract
BACKGROUND:
Q fever fatigue syndrome (QFS) is a state of prolonged fatigue following around 20% of acute Q fever cases. It is thought that chronic inflammation plays a role in its aetiology. To test this hypothesis we measured circulating cytokines and the exvivo cytokine production in patients with QFS and compared to various control groups.
MATERIALS/METHODS:
Peripheral blood mononuclear cells (PBMCs), whole blood, and serum were collected from 20 QFS patients, 19 chronic fatigue syndrome (CFS) patients, 19 Q fever seropositive controls, and 25 age- and sex-matched healthy controls. Coxiella-specific ex-vivo production of tumor necrosis factor (TNF)α, interleukin (IL)-1β, IL-6, and interferon (IFN) was measured, together with a total of 92 circulating inflammatory proteins.
RESULTS:
PBMCs of QFS patients produced more IL-6 (P = 0.0001), TNFα (P = 0.0002), and IL-1β (P = 0.0005) than the various control groups when stimulated with Coxiella antigen. QFS patients had distinct differences in circulating inflammatory markers compared to the other groups, including higher concentrations of circulating IL-6 and IFNγ.
CONCLUSION:
QFS patients showed signs of chronic inflammation compared to asymptomatic Q fever seropositive controls, CFS patients, and healthy controls, of which the monocyte-derived cytokines TNFα, IL-1β, and especially IL-6, are likely crucial components.
Copyright © 2019. Published by Elsevier Ltd.
KEYWORDS:
CFS, chronic fatigue syndrome; IFNγ; IL-1β; IL-6; Proximity Extension Assay; QFS, Q fever fatigue syndrome; TNFα; cytokines
PMID:
30684502
DOI:
10.1016/j.jinf.2019.01.006
Cytokine profiles in patients with Q fever fatigue syndrome.
Raijmakers RPH1, Koeken V2, Jansen AFM3, Keijmel SP4, Roerink ME5, Joosten LAB6, Netea MG7, van der Meer JWM8, Bleeker-Rovers CP9.
Author information
Abstract
BACKGROUND:
Q fever fatigue syndrome (QFS) is a state of prolonged fatigue following around 20% of acute Q fever cases. It is thought that chronic inflammation plays a role in its aetiology. To test this hypothesis we measured circulating cytokines and the exvivo cytokine production in patients with QFS and compared to various control groups.
MATERIALS/METHODS:
Peripheral blood mononuclear cells (PBMCs), whole blood, and serum were collected from 20 QFS patients, 19 chronic fatigue syndrome (CFS) patients, 19 Q fever seropositive controls, and 25 age- and sex-matched healthy controls. Coxiella-specific ex-vivo production of tumor necrosis factor (TNF)α, interleukin (IL)-1β, IL-6, and interferon (IFN) was measured, together with a total of 92 circulating inflammatory proteins.
RESULTS:
PBMCs of QFS patients produced more IL-6 (P = 0.0001), TNFα (P = 0.0002), and IL-1β (P = 0.0005) than the various control groups when stimulated with Coxiella antigen. QFS patients had distinct differences in circulating inflammatory markers compared to the other groups, including higher concentrations of circulating IL-6 and IFNγ.
CONCLUSION:
QFS patients showed signs of chronic inflammation compared to asymptomatic Q fever seropositive controls, CFS patients, and healthy controls, of which the monocyte-derived cytokines TNFα, IL-1β, and especially IL-6, are likely crucial components.
Copyright © 2019. Published by Elsevier Ltd.
KEYWORDS:
CFS, chronic fatigue syndrome; IFNγ; IL-1β; IL-6; Proximity Extension Assay; QFS, Q fever fatigue syndrome; TNFα; cytokines
PMID:
30684502
DOI:
10.1016/j.jinf.2019.01.006