CIRCULATING PROINFLAMMATORY CYTOKINES (IL-1-BETA, TNF-ALPHA, AND IL-6) AND IL-1 RECEPTOR ANTAGONIST (IL-1RA) IN FULMINANT HEPATIC-FAILURE AND ACUTE HEPATITIS

被引:1
|
作者
SEKIYAMA, KD
YOSHIBA, M
THOMSON, AW
机构
[1] UNIV PITTSBURGH, MED CTR, DEPT SURG, PITTSBURGH TRANSPLANT INST, PITTSBURGH, PA 15213 USA
[2] UNIV PITTSBURGH, MED CTR, DEPT MOLEC GENET & BIOCHEM, PITTSBURGH, PA USA
[3] SHOWA UNIV, FUJIGAOKA HOSP, DEPT MED, DIV GASTROENTEROL, YOKOHAMA, JAPAN
来源
CLINICAL AND EXPERIMENTAL IMMUNOLOGY | 1994年 / 98卷 / 01期
关键词
CYTOKINES; IL-1 RECEPTOR ANTAGONIST; FULMINANT HEPATITIC FAILURE;
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Fulminant hepatic failure (FHF) is characterized by massive necroinflammation of the liver tissue and is associated with high mortality. Serum concentrations of IL-1 beta, tumour necrosis factor-alpha (TNF-alpha), IL-6 and IL-1 receptor antagonist (IL-1Ra) were measured in 30 patients with FHF and in 23 patients with acute hepatitis (AH) before start of treatment and in 23 healthy controls. Levels of all four molecules were increased significantly in FHF compared with AH, in which values were higher than in the healthy controls. High serum levels of IL-1 beta and a significantly reduced ratio of IL-1Ra to IL-1 beta (IL-1Ra/IL-1 beta) were observed in FHF patients who subsequently died compared with subjects who survived. TNF-alpha and IL-6 concentrations were correlated with levels of human hepatocyte growth factor (hHGF), an index of hepatocyte regeneration. Although serum cytokine levels varied considerably between patients within each group studied, it is suggested that the striking elevation in proinflammatory cytokine levels in FHF may reflect both the insufficiency of hepatitis virus elimination and a failure to control a vicious cytokine cascade leading to overwhelming hepatocyte destruction rather than regeneration. The high cytokine levels observed in these patients and the significantly elevated IL-1Ra/IL-1 beta ratio in FHF patients who survived compared with those who did not suggest the possible therapeutic use of cytokine antagonists for the control of this life-threatening disease.
引用
收藏
页码:71 / 77
页数:7
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