Mercuric chloride-induced vasculitis in the Brown Norway rat:: αβ T cell-dependent and -independent phases -: Role of the mast cell

被引:0
作者
Kiely, PDW
Pecht, I
Oliveira, DBG
机构
[1] Univ London St Georges Hosp, Sch Med, Div Renal Med, London SW17 0RE, England
[2] Weizmann Inst Sci, Dept Clin Immunol, IL-76100 Rehovot, Israel
基金
英国惠康基金;
关键词
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
Mercuric chloride induces a necrotizing vasculitis in the Brown Norway (BN) rat, This occurs in two phases, between 1 and 5 days (early) and between 12 and 20 days (late) after initiation of HgCl2. One outbred and four inbred rat strains were found to be susceptible to early vasculitis, but only the BN strain developed late vasculitis. In the BN strain, treatment with the mAb R73 (anti-alpha beta TCR) inhibited T cell function, completely prevented the late vasculitis, but had no effect against early vasculitis, indicating that early and late vasculitis is controlled by different genetic and cellular mechanisms, The role of the mast cell in the alpha beta T cell-independent early phase was studied, Serum concentrations of rat mast cell protease II rose following HgCl2 treatment, indicating mast cell degranulation. The reagents Doxantrazole and the mAb G63, which suppress mast cell secretory responses, also prevented the rise in rat mast cell protease II and significantly reduced the early vasculitis, The demonstration of an alpha beta T cell-dependent phase supports previous experimental data that T cells play an important role in the pathogenesis of vasculitis. The presence of an earlier alpha beta T cell-independent phase is a unique observation, The data support a role for the mast cell in the early vasculitis.
引用
收藏
页码:5100 / 5106
页数:7
相关论文
共 47 条
[1]  
ASKENASE PW, 1983, J IMMUNOL, V131, P2687
[2]   IMMUNOPATHOLOGY OF PARASITIC DISEASES - INVOLVEMENT OF BASOPHILS AND MAST-CELLS [J].
ASKENASE, PW .
SPRINGER SEMINARS IN IMMUNOPATHOLOGY, 1980, 2 (04) :417-442
[3]   INTERLEUKIN-3-DEPENDENT AND INTERLEUKIN-3-INDEPENDENT MAST-CELLS STIMULATED WITH IGE AND ANTIGEN EXPRESS MULTIPLE CYTOKINES [J].
BURD, PR ;
ROGERS, HW ;
GORDON, JR ;
MARTIN, CA ;
JAYARAMAN, S ;
WILSON, SD ;
DVORAK, AM ;
GALLI, SJ ;
DORF, ME .
JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 170 (01) :245-257
[4]   MERCURIC CHLORIDE-INDUCED ANTI-GLOMERULAR BASEMENT-MEMBRANE ANTIBODIES IN RAT - GENETIC-CONTROL [J].
DRUET, E ;
SAPIN, C ;
GUNTHER, E ;
FEINGOLD, N ;
DRUET, P .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1977, 7 (06) :348-351
[5]  
ESNAULT VLM, 1992, LAB INVEST, V67, P114
[6]  
Geba GP, 1996, J IMMUNOL, V157, P557
[7]   INTERLEUKIN-4 GENE-EXPRESSION IN MERCURY-INDUCED AUTOIMMUNITY [J].
GILLESPIE, KM ;
QASIM, FJ ;
TIBBATTS, LM ;
THIRU, S ;
OLIVEIRA, DBG ;
MATHIESON, PW .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 1995, 41 (03) :268-272
[8]   MAST-CELLS AS A SOURCE OF MULTIFUNCTIONAL CYTOKINES [J].
GORDON, JR ;
BURD, PR ;
GALLI, SJ .
IMMUNOLOGY TODAY, 1990, 11 (12) :458-464
[9]   T cell responses to myeloperoxidase (MPO) and proteinase 3 (PR3) in patients with systemic vasculitis [J].
Griffith, ME ;
Coulthart, A ;
Pusey, CD .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 1996, 103 (02) :253-258
[10]   DECREASED FREQUENCY OF HLA-DR13DR6 IN WEGENERS GRANULOMATOSIS [J].
HAGEN, EC ;
STEGEMAN, CA ;
DAMARO, J ;
SCHREUDER, GMT ;
LEMS, SPM ;
TERVAERT, JWC ;
DEJONG, GM ;
HENE, RJ ;
KALLENBERG, CGM ;
DAHA, MR ;
VANDERWOUDE, FJ .
KIDNEY INTERNATIONAL, 1995, 48 (03) :801-805