Circulating levels of IL-11 and leukaemia inhibitory factor (LIF) do not significantly participate in the production of acute-phase proteins by the liver

被引:18
作者
Gabay, C
Singwe, M
Genin, B
Meyer, O
Mentha, G
LeCoultre, C
Vischer, T
Guerne, PA
机构
[1] HOP CANTONAL GENEVA,DIV RHEUMATOL,CH-1211 GENEVA,SWITZERLAND
[2] HOP CANTONAL UNIV GENEVA,CLIN CHIRURG PEDIAT,GENEVA,SWITZERLAND
[3] HOP CANTONAL UNIV GENEVA,CHIRURG DIGEST CLIN,CH-1211 GENEVA,SWITZERLAND
[4] CHU BICHAT CLAUDE BERNARD,RHUMATOL CLIN,PARIS,FRANCE
关键词
acute-phase proteins; IL-11; leukaemia inhibitory factor; IL-6; human primary hepatocytes;
D O I
10.1046/j.1365-2249.1996.d01-757.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To investigate the contribution of IL-11 and LIF to acute-phase protein (APP) production, we first analysed the effects of IL-11 and LIF on production of C-reactive protein (CRP), fibrinogen, and haptoglobin by human primary hepatocytes. We also measured the serum levels of IL-11, LIF, and CRP in serum from patients with inflammatory rheumatic diseases to assess the role of these cytokines in the APP response in vivo. We included patients with conditions associated with a high APP response such as rheumatoid arthritis (RA) or spondylarthropathy (SpA), and others usually associated with a weak APP response such as systemic lupus erythematosus (SLE), in order to investigate whether these cytokines could account for the differences in APP responses. Our results showed that IL-11 and LIF induced only minimal stimulation on production of APP by human primary hepatocytes compared with IL-6, known as the major inducer. Serum levels of CRP were elevated in RA and SpA, and significantly higher than in SLE patients. Despite the presence of a high APP response in some of our patients and despite the fact that we used sensitive assays to measure IL-11 and LIF, serum levels of both cytokines were not detected in any of the tested sera. In conclusion, our results show that circulating levels of IL-11 or LIF do not contribute significantly to the production of APP in vivo, and that they do not account for the difference in APP response between SLE and other inflammatory rheumatic diseases.
引用
收藏
页码:260 / 265
页数:6
相关论文
共 41 条
[1]   CYTOKINE PROFILE IN SYSTEMIC LUPUS-ERYTHEMATOSUS, RHEUMATOID-ARTHRITIS, AND OTHER RHEUMATIC DISEASES [J].
ALJANADI, M ;
ALBALLA, S ;
ALDALAAN, A ;
RAZIUDDIN, S .
JOURNAL OF CLINICAL IMMUNOLOGY, 1993, 13 (01) :58-67
[2]   THE AMERICAN-RHEUMATISM-ASSOCIATION 1987 REVISED CRITERIA FOR THE CLASSIFICATION OF RHEUMATOID-ARTHRITIS [J].
ARNETT, FC ;
EDWORTHY, SM ;
BLOCH, DA ;
MCSHANE, DJ ;
FRIES, JF ;
COOPER, NS ;
HEALEY, LA ;
KAPLAN, SR ;
LIANG, MH ;
LUTHRA, HS ;
MEDSGER, TA ;
MITCHELL, DM ;
NEUSTADT, DH ;
PINALS, RS ;
SCHALLER, JG ;
SHARP, JT ;
WILDER, RL ;
HUNDER, GG .
ARTHRITIS AND RHEUMATISM, 1988, 31 (03) :315-324
[3]   ONCOSTATIN-M STIMULATES PROLIFERATION IN B9 HYBRIDOMA CELLS - POTENTIAL ROLE OF ONCOSTATIN-M IN PLASMACYTOMA DEVELOPMENT [J].
BARTON, BE ;
JACKSON, JV ;
LEE, F ;
WAGNER, J .
CYTOKINE, 1994, 6 (02) :147-153
[4]  
BAUMANN H, 1989, J IMMUNOL, V143, P1163
[5]  
BAUMANN H, 1990, MOL BIOL MED, V7, P147
[6]  
BAUMANN H, 1991, J BIOL CHEM, V266, P20424
[7]   INTERLEUKIN-6 IS THE MAJOR REGULATOR OF ACUTE PHASE PROTEIN-SYNTHESIS IN ADULT HUMAN HEPATOCYTES [J].
CASTELL, JV ;
GOMEZLECHON, MJ ;
DAVID, M ;
ANDUS, T ;
GEIGER, T ;
TRULLENQUE, R ;
FABRA, R ;
HEINRICH, PC .
FEBS LETTERS, 1989, 242 (02) :237-239
[8]   THE EUROPEAN-SPONDYLARTHROPATHY-STUDY-GROUP PRELIMINARY CRITERIA FOR THE CLASSIFICATION OF SPONDYLARTHROPATHY [J].
DOUGADOS, M ;
VANDERLINDEN, S ;
JUHLIN, R ;
HUITFELDT, B ;
AMOR, B ;
CALIN, A ;
CATS, A ;
DIJKMANS, B ;
OLIVIERI, I ;
PASERO, G ;
VEYS, E ;
ZEIDLER, H .
ARTHRITIS AND RHEUMATISM, 1991, 34 (10) :1218-1227
[9]  
GABAY C, 1993, J RHEUMATOL, V20, P815
[10]  
GABAY C, 1995, CLIN EXP IMMUNOL, V100, P306