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Pediatr Infect Dis J ; 14(7): 594-8, 1995 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-7567288

RESUMO

Hemolytic uremic syndrome (HUS) is thought to be a vascular endothelial injury disease. The mechanism of injury is unknown although verocytotoxins (Shiga-like toxins (SLTs)) are known to be associated with it. Recent evidence suggests that in vitro treatment of some endothelial cells with tumor necrosis factor alpha (TNF-alpha) dramatically increases their susceptibility to SLTs. We studied 25 children with HUS, 63 children with SLT-positive bloody diarrhea, 62 children with bloody diarrhea not associated with SLTs and 39 children admitted for elective surgery, included as an age- and season-matched control group. The TNF-alpha concentrations were found to be significantly elevated in children with HUS (range, 1 to 95 pg/ml; geometric mean, 32.2 pg/ml) compared with the healthy controls (range, 0 to 53 pg/ml; mean, 12.5 pg/ml; P < 0.001). Because it is hypothesized that TNF-alpha elevation might precede development of HUS, we also studied children with blood diarrhea. The TNF-alpha serum concentrations were significantly higher during the first 10 days after onset of bloody diarrhea than after the first 10 days (P < 0.02). Such elevation could be associated with vascular endothelial glycolipid receptor up-regulation and increased susceptibility to the effects of SLTs.


Assuntos
Síndrome Hemolítico-Urêmica/sangue , Síndrome Hemolítico-Urêmica/fisiopatologia , Fator de Necrose Tumoral alfa/análise , Argentina , Estudos de Casos e Controles , Pré-Escolar , Diarreia/etiologia , Fezes/microbiologia , Feminino , Síndrome Hemolítico-Urêmica/complicações , Humanos , Imunoensaio , Lactente , Masculino , Prognóstico
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