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Pathophysiologic and Prognostic Role of Cytokines in Dengue Hemorrhagic Fever
Author(s) -
Delia B. Bethell,
Karin Flobbe,
Cao Xuan Thanh Phuong,
Nicholas P. J. Day,
Pham Phuong,
Wim A. Buurman,
Mary Jane Cardosa,
Nicholas J. White,
Dominic Kwiatkowski
Publication year - 1998
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 - 10.1086/517807
Subject(s) - dengue fever , shock (circulatory) , medicine , pathophysiology , vascular permeability , cytokine storm , immunology , cytokine , endothelial activation , tumor necrosis factor alpha , pathogenesis , gastroenterology , inflammation , disease , infectious disease (medical specialty) , covid-19
Dengue shock syndrome is a severe complication of dengue hemorrhagic fever (DHF), characterized by a massive increase in vascular permeability. Plasma cytokine concentrations were prospectively studied in 443 Vietnamese children with DHF, of whom 6 died. Shock was present in 188 children on admission to hospital, and in 71 children it developed later. Contrary to expectations, certain inflammatory markers (interleukin-6 and soluble intercellular adhesion molecule-1) were lower in the group with shock, and this may reflect the general loss of protein from the circulation due to capillary leakage. Only soluble tumor necrosis factor receptor (TNFR) levels showed a consistent positive relationship with disease severity. In patients with suspected DHF without shock, admission levels of sTNFR-75 in excess of 55 pg/mL predicted the subsequent development of shock, with a relative risk of 5.5 (95% confidence interval, 2.3-13.2). Large-scale release of soluble TNFR may be an early and specific marker of the endothelial changes that cause dengue shock syndrome.

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