Cytokine gene expression in the BE rat pancreas: Natural course and impact of bacterial vaccines

被引:48
作者
Kolb, H [1 ]
WorzPagenstert, U [1 ]
Kleemann, R [1 ]
Rothe, H [1 ]
Rowsell, P [1 ]
Scott, FW [1 ]
机构
[1] HLTH CANADA,NUTR RES DIV,OTTAWA,ON K1A 0L2,CANADA
关键词
BE rat; insulitis; cytokines; inducible NO synthase; BCG; tetanus toroid; lipopolysaccharide;
D O I
10.1007/s001250050597
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In diabetes prone BE rat pancreas the Th1/Th2 cytokine balance and the expression of inducible nitric oxide synthase (iNOS) was determined by mRNA analysis before and after the onset of insulitis. Specific mRNA was amplified by reverse transcriptase polymerase chain reaction, quantitated with radiolabelled probes by phosphoimaging and calibrated with the amount of co-amplified beta-actin mRNA. At 50 days of age, prior to recognizeable insulitis, there was already significantly enhanced expression of both, Th1 and Th2 cytokines, and of iNOS mRNA, when compared to Wistar rat pancreas (p < 0.001). This supports the concept of an inconspicuous early phase of islet infiltration by single immunocytes, called single eel insulitis. At 70 days of age mononuclear infiltration of islets had begun and was associated with upregulation of interferon gamma (IFN gamma) and iNOS, but downregulation of interleukin-10 and transforming growth factor beta mRNA (p < 0.001). These findings correlate the onset of insulitis with a shift of the Th1/Th2 cytokine balance towards Th1 cell reactivity. Indeed there was a close correlation of the Th1/Th2 cytokine ratio but not of absolute IFN gamma mRNA levels with the insulitis score. Vaccination at day 50 with tetanus toroid did not affect cytokine gene expression while diphtheria toroid and even more strongly BCG administration induced a shift towards Th2 reactivity (p < 0.001) while iNOS mRNA was decreased (p < 0.01). Oral dosing with immunostimulatory components of Escherichia coli also changed the quality of inflammation. Oral lipopolysaccharide (LPS) from E. coli and OM-89, an endotoxin free extract containing immunostimulatory glycolipopeptides and heat shock protein (hsp) 65, both downregulated IFN gamma mRNA while only OM-89 in addition suppressed INOS mRNA and enhanced Th2 cytokine gene expression (p < 0.001). We conclude that the onset of insulitis is associated with a shift towards Th1 cytokine and iNOS gene expression. Diphtheria toroid and BCG vaccination stimulates Th2 reactivity but does not: downregulate Th1. The latter can be achieved through oral administration of LPS or a glycopeptide fraction (OM-89) from E. coli.
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收藏
页码:1448 / 1454
页数:7
相关论文
共 41 条
[1]   INSULIN-DEPENDENT DIABETES IN THE NOD MOUSE MODEL .2. BETA-CELL DESTRUCTION IN AUTOIMMUNE DIABETES IS A TH2 AND NOT A TH1 MEDIATED EVENT [J].
ANDERSON, JT ;
CORNELIUS, JG ;
JARPE, AJ ;
WINTER, WE ;
PECK, AB .
AUTOIMMUNITY, 1993, 15 (02) :113-122
[2]   EFFECT OF CYCLOSPORINE ON PANCREATIC EVENTS AND DEVELOPMENT OF DIABETES IN BB/EDINBURGH RATS [J].
BONE, AJ ;
WALKER, R ;
VAREY, AM ;
COOKE, A ;
BAIRD, JD .
DIABETES, 1990, 39 (04) :508-514
[3]   ESSENTIAL ROLE FOR INTERFERON-GAMMA AND INTERLEUKIN-6 IN AUTOIMMUNE INSULIN-DEPENDENT DIABETES IN NOD/WEHI MICE [J].
CAMPBELL, IL ;
KAY, TWH ;
OXBROW, L ;
HARRISON, LC .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 87 (02) :739-742
[4]  
GEPTS W, 1985, DIABETIC PANCREAS, P337
[5]   MACROPHAGE INFILTRATION PRECEDES AND IS A PREREQUISITE FOR LYMPHOCYTIC INSULITIS IN PANCREATIC-ISLETS OF PRE-DIABETIC BB RATS [J].
HANENBERG, H ;
KOLBBACHOFEN, V ;
KANTWERKFUNKE, G ;
KOLB, H .
DIABETOLOGIA, 1989, 32 (02) :126-134
[6]   PREVENTION OF OVERT DIABETES AND INSULITIS IN NOD MICE BY A SINGLE BCG VACCINATION [J].
HARADA, M ;
KISHIMOTO, Y ;
MAKINO, S .
DIABETES RESEARCH AND CLINICAL PRACTICE, 1990, 8 (02) :85-89
[7]   ISLET EXPRESSION OF INTERFERON-ALPHA PRECEDES DIABETES IN BOTH THE BB RAT AND STREPTOZOTOCIN-TREATED MICE [J].
HUANG, XJ ;
HULTGREN, B ;
DYBDAL, N ;
STEWART, TA .
IMMUNITY, 1994, 1 (06) :469-478
[8]  
JIANG Z, 1991, J IMMUNOL, V146, P2990
[9]  
KALLMANN B, 1995, AUTOIMMUNITY, V21, P52
[10]  
KALLMANN BA, 1996, IN PRESS ARCH DERMAT