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Systemic Inflammatory Responses in African Tick‐Bite Fever
Author(s) -
Mogens Jensenius,
Thor Ueland,
PierreEdouard Fournier,
Frank Brosstad,
Eva Stylianou,
Sirkka Vene,
Bjørn Myrvang,
Didier Raoult,
Pål Aukrust
Publication year - 2003
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/368415
Subject(s) - immunology , rickettsiosis , macrophage inflammatory protein , tumor necrosis factor alpha , inflammation , medicine , von willebrand factor , chemokine , cytokine , proinflammatory cytokine , antibody , serology , platelet
Information regarding the inflammatory response in African tick-bite fever (ATBF), an emerging spotted-fever-group rickettsiosis, in international travelers to sub-Saharan Africa, is scarce. Plasma/serum levels of von Willebrand factor (vWF), soluble (s) E-selectin, tumor necrosis factor-alpha, interleukin (IL)-6, interferon-gamma, IL-10, IL-13, IL-8, RANTES, macrophage inflammatory protein-1alpha, and C-reactive protein were studied, at both first presentation and follow-up, in 15 patients with travel-associated ATBF and in 14 healthy travelers who served as control subjects. Our main and novel findings are the following: (1) patients with ATBF had increased levels of vWF and sE-selectin, with a subsequent decrease at follow-up; (2) with the exception of IFN-gamma, levels of cytokines and chemokines were also increased in these patients at the first presentation; and (3) IL-10 and IL-13 tended to increase during follow-up, whereas most of the inflammatory cytokines decreased. The induction of these mediators and the balance between them may be critical both for the regulation of inflammation and for protective immunity in ATBF.

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