RELEASE OF SOLUBLE RECEPTORS FOR TUMOR-NECROSIS-FACTOR (TNF) IN RELATION TO CIRCULATING TNF DURING EXPERIMENTAL ENDOTOXINEMIA

被引:232
作者
SPINAS, GA
KELLER, U
BROCKHAUS, M
机构
[1] F HOFFMANN LA ROCHE & CO LTD,PHARMACEUT RES NEW TECHNOL,BLDG 69-214,CH-4002 BASEL,SWITZERLAND
[2] UNIV HOSP BASEL,DEPT INTERNAL MED & RES,CH-4031 BASEL,SWITZERLAND
关键词
LIPOPOLYSACCHARIDE; TUMOR NECROSIS FACTOR BINDING PROTEIN; HUMAN; IBUPROFEN; CYCLOOXYGENASE INHIBITOR;
D O I
10.1172/JCI115891
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Serial plasma samples from human volunteers obtained after intravenous administration of Escherichia coli endotoxin were analyzed for the presence of circulating soluble tumor necrosis factor receptors (sTNFR). A four- to fivefold increase of type A (p75) and type B (p55) sTNFR was observed 3 h after endotoxin challenge. Pretreatment of the volunteers with ibuprofen before the injection of endotoxin resulted in a slight increase (3.87+/-0.2 vs. 3.27+/-0.3 ng/ml) and temporal shift of sTNFR-A release concurrent to a marked augmentation of TNF levels (603+/-118 vs. 338+/-56 pg/ml) as compared to the group without ibuprofen pretreatment. There was a significant correlation between peak sTNFR-A levels and peak TNF levels in the individual probands (r = 0.52, P = 0.04). On the contrary, release kinetics and plasma concentrations of sTNFR-B were identical in both groups (7.38+/-0.69 vs. 7.44+/-0.33 ng/ml) and no correlation with individual TNF levels was observed. The amount of sTNFR liberated upon endotoxin challenge was not sufficient to block TNF-mediated cytotoxic effects. Our data indicate that the release in vivo of type A and type B sTNFR upon a short exposure to endotoxin is regulated differently.
引用
收藏
页码:533 / 536
页数:4
相关论文
共 26 条
[1]  
ADERKA D, 1991, CANCER RES, V51, P5602
[2]   IDENTIFICATION OF 2 TYPES OF TUMOR-NECROSIS-FACTOR RECEPTORS ON HUMAN CELL-LINES BY MONOCLONAL-ANTIBODIES [J].
BROCKHAUS, M ;
SCHOENFELD, HJ ;
SCHLAEGER, EJ ;
HUNZIKER, W ;
LESSLAUER, W ;
LOETSCHER, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (08) :3127-3131
[3]  
DEMBIC Z, 1990, Cytokine, V2, P231, DOI 10.1016/1043-4666(90)90022-L
[4]   HIGH-LEVELS OF CIRCULATING SOLUBLE RECEPTORS FOR TUMOR-NECROSIS-FACTOR IN HAIRY-CELL LEUKEMIA AND TYPE-B CHRONIC LYMPHOCYTIC-LEUKEMIA [J].
DIGEL, W ;
PORZSOLT, F ;
SCHMID, M ;
HERRMANN, F ;
LESSLAUER, W ;
BROCKHAUS, M .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 89 (05) :1690-1693
[5]   EVIDENCE FOR DIFFERENT EFFECTS OF SOLUBLE TNF-RECEPTORS ON VARIOUS TNF MEASUREMENTS IN HUMAN BIOLOGICAL-FLUIDS [J].
ENGELBERTS, I ;
STEPHENS, S ;
FRANCOT, GJM ;
VANDERLINDEN, CJ ;
BUURMAN, WA .
LANCET, 1991, 338 (8765) :515-516
[6]  
ENGELMANN H, 1990, J BIOL CHEM, V265, P1531
[7]   TUMOR-NECROSIS-FACTOR (CACHECTIN) AS AN ESSENTIAL MEDIATOR IN MURINE CEREBRAL MALARIA [J].
GRAU, GE ;
FAJARDO, LF ;
PIGUET, PF ;
ALLET, B ;
LAMBERT, PH ;
VASSALLI, P .
SCIENCE, 1987, 237 (4819) :1210-1212
[8]  
HOHMANN HP, 1990, J BIOL CHEM, V265, P22409
[9]  
HOHMANN HP, 1989, J BIOL CHEM, V264, P14927
[10]   A 2ND TUMOR-NECROSIS-FACTOR RECEPTOR GENE-PRODUCT CAN SHED A NATURALLY-OCCURRING TUMOR-NECROSIS-FACTOR INHIBITOR [J].
KOHNO, T ;
BREWER, MT ;
BAKER, SL ;
SCHWARTZ, PE ;
KING, MW ;
HALE, KK ;
SQUIRES, CH ;
THOMPSON, RC ;
VANNICE, JL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (21) :8331-8335