Pathophysiological mechanisms of TNF during intoxication with natural or man-made toxins

被引:73
作者
Schümann, J [1 ]
Tiegs, G [1 ]
机构
[1] Univ Erlangen Nurnberg, Inst Expt & Clin Pharmacol & Toxicol, D-91054 Erlangen, Germany
关键词
inflammation; liver; lymphocytes;
D O I
10.1016/S0300-483X(99)00087-6
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Intoxication with different natural toxins or man-made toxicants has been associated with the induction of tumor necrosis factor alpha (TNF). These include endotoxin, superantigens, Pseudomonas aeruginosa exotoxin A, bacterial DNA, T cell stimulatory agents such as agonistic anti-CD3 mAbs or concanavalin A, alpha-amanitin, paracetamol, ethanol, carbon tetrachloride, dioxin, and dimethylnitrosamine. In this paper we compile and discuss the current knowledge on the pathophysiological role of TNF during intoxication with all mentioned toxins and toxicants. A possible role of gut-derived endotoxin in several TNF-dependent toxic events has been considered. The development of pharmaceuticals that selectively interfere with the detrimental pathways induced by TNF during intoxication with bacteria, viruses, drugs, or other chemicals requires detailed knowledge of the signaling pathways originating from the two TNF receptors (TNFR1 and TNFR2). Major characteristics of these signaling pathways are described and put together. (C) 1999 Published by Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:103 / 126
页数:24
相关论文
共 169 条
[1]   RELEASE OF TUMOR NECROSIS FACTOR, INTERLEUKIN-2, AND GAMMA-INTERFERON IN SERUM AFTER INJECTION OF OKT3 MONOCLONAL-ANTIBODY IN KIDNEY-TRANSPLANT RECIPIENTS [J].
ABRAMOWICZ, D ;
SCHANDENE, L ;
GOLDMAN, M ;
CRUSIAUX, A ;
VEREERSTRAETEN, P ;
DEPAUW, L ;
WYBRAN, J ;
KINNAERT, P ;
DUPONT, E ;
TOUSSAINT, C .
TRANSPLANTATION, 1989, 47 (04) :606-608
[2]   INACTIVATION OF KUPFFER CELLS PREVENTS EARLY ALCOHOL-INDUCED LIVER-INJURY [J].
ADACHI, Y ;
BRADFORD, BU ;
GAO, WS ;
BOJES, HK ;
THURMAN, RG .
HEPATOLOGY, 1994, 20 (02) :453-460
[3]   KUPFFER CELLS FROM CARBON-TETRACHLORIDE INJURED RAT LIVERS PRODUCE CHEMOTACTIC FACTORS FOR FIBROBLASTS AND MONOCYTES - THE ROLE OF TUMOR-NECROSIS-FACTOR-ALPHA [J].
ARMENDARIZBORUNDA, J ;
SEYER, JM ;
POSTLETHWAITE, AE ;
KANG, AH .
HEPATOLOGY, 1991, 14 (05) :895-900
[4]   An essential role for NF-kappa B in preventing TNF-alpha-induced cell death [J].
Beg, AA ;
Baltimore, D .
SCIENCE, 1996, 274 (5288) :782-784
[5]   DISTRIBUTION AND KINETICS OF SUPERANTIGEN-INDUCED CYTOKINE GENE-EXPRESSION IN MOUSE SPLEEN [J].
BETTE, M ;
SCHAFER, MKH ;
VANROOIJEN, N ;
WEIHE, E ;
FLEISCHER, B .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (05) :1531-1540
[6]   PASSIVE-IMMUNIZATION AGAINST CACHECTIN TUMOR NECROSIS FACTOR PROTECTS MICE FROM LETHAL EFFECT OF ENDOTOXIN [J].
BEUTLER, B ;
MILSARK, IW ;
CERAMI, AC .
SCIENCE, 1985, 229 (4716) :869-871
[7]  
BEUTLER BA, 1985, J IMMUNOL, V135, P3972
[8]   ENDOTOXIN INDUCED HEPATIC-NECROSIS IN RATS ON AN ALCOHOL DIET [J].
BHAGWANDEEN, BS ;
APTE, M ;
MANWARRING, L ;
DICKESON, J .
JOURNAL OF PATHOLOGY, 1987, 152 (01) :47-53
[9]   DUAL ROLE OF THE P75 TUMOR-NECROSIS-FACTOR (TNF) RECEPTOR IN TNF CYTOTOXICITY [J].
BIGDA, J ;
BELETSKY, I ;
BRAKEBUSCH, C ;
VARFOLOMEEV, Y ;
ENGELMANN, H ;
BIGDA, J ;
HOLTMANN, H ;
WALLACH, D .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (02) :445-460
[10]   ROLE OF PROINFLAMMATORY CYTOKINES IN ACETAMINOPHEN HEPATOTOXICITY [J].
BLAZKA, ME ;
WILMER, JL ;
HOLLADAY, SD ;
WILSON, RE ;
LUSTER, MI .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1995, 133 (01) :43-52