INHIBITION OF INVITRO IMMUNOGLOBULIN PRODUCTION BY RAPAMYCIN

被引:72
作者
LUO, HY
CHEN, HF
DALOZE, P
CHANG, JY
STLOUIS, G
WU, JP
机构
[1] UNIV MONTREAL,NOTRE DAME HOSP RES CTR,NEPHROL & TRANSPLANTAT IMMUNOL LAB,1560 SHERBROOKE ST E,MONTREAL H2L 4M1,QUEBEC,CANADA
[2] UNIV MONTREAL,NOTRE DAME HOSP RES CTR,SURG RES LAB,MONTREAL H2L 4M1,QUEBEC,CANADA
[3] WYETH AYERST RES,PRINCETON,NJ 08543
关键词
D O I
10.1097/00007890-199205000-00019
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Like FK506, rapamycin, a structural analog of FK506, is a strong immunosuppressant. The immunosuppressive effect of Rapa in in vitro IgG, IgM, and IgA production by human lymphocytes was examined in this study. To inhibit spontaneous or pokeweed mitogen-stimulated production of Ig by human peripheral blood lymphocytes, about one thousandfold lower concentrations of Rapa (IC50 = 0.3 nM-2 nM) were required than of cyclosporine (IC50 = 0.3-mu-M-2-mu-M). T cells were the direct targets of Rapa, because preincubation of T cells with Rapa abolished the T cells helper effect to T-dependent Ig production. Rapa also had direct suppressive effect on B cells, since Rapa suppressed IgG production by pure B cells stimulated with IL2 and Staphylococcus aureus Cowan I. Kinetic studies measuring IgG production and cell proliferation revealed that Rapa acted at the activation stage of T and B cells. Exogenous IL2 substantially reversed the inhibitory effect of CsA but not that of Rapa in Ig production. This study is the first report on the strong suppressive effect of Rapa on human humoral immune response with a quantitative comparison with that of CsA. The underlying mechanisms are also explored. The results indicate the potential usefulness of this drug in treatment of presensitized transplantation patients, with whom cytotoxic Ab is a major obstacle to a successful transplantation.
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页码:1071 / 1076
页数:6
相关论文
共 26 条
[1]   RAPAMYCIN (AY-22,989), A NEW ANTIFUNGAL ANTIBIOTIC .3. INVITRO AND INVIVO EVALUATION [J].
BAKER, H ;
SIDOROWICZ, A ;
SEHGAL, SN ;
VEZINA, C .
JOURNAL OF ANTIBIOTICS, 1978, 31 (06) :539-545
[2]   2 DISTINCT SIGNAL TRANSMISSION PATHWAYS IN LYMPHOCYTES-T ARE INHIBITED BY COMPLEXES FORMED BETWEEN AN IMMUNOPHILIN AND EITHER FK506 OR RAPAMYCIN [J].
BIERER, BE ;
MATTILA, PS ;
STANDAERT, RF ;
HERZENBERG, LA ;
BURAKOFF, SJ ;
CRABTREE, G ;
SCHREIBER, SL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (23) :9231-9235
[3]   PREEXPOSURE OF RESTING B-CELLS TO INTERFERON-GAMMA ENHANCES THEIR PROLIFERATIVE RESPONSE TO SUBSEQUENT ACTIVATION SIGNALS [J].
BOYD, AW ;
TEDDER, TF ;
GRIFFIN, JD ;
FREEDMAN, AS ;
FISHER, DC ;
DALEY, J ;
NADLER, LM .
CELLULAR IMMUNOLOGY, 1987, 106 (02) :355-365
[4]  
CALNE RY, 1989, LANCET, V2, P227
[5]  
CHEN HF, 1991, TRANSPLANT P, V23, P2241
[6]  
DEPAULIS A, 1991, J IMMUNOL, V146, P2374
[7]  
DUMONT FJ, 1990, J IMMUNOL, V144, P251
[8]   ACTIVITY OF RAPAMYCIN (AY-22,989) AGAINST TRANSPLANTED TUMORS [J].
ENG, CP ;
SEHGAL, SN ;
VEZINA, C .
JOURNAL OF ANTIBIOTICS, 1984, 37 (10) :1231-1237
[9]  
FARGEAS C, 1990, J IMMUNOL, V145, P4053
[10]  
FINKELMAN FD, 1988, J IMMUNOL, V140, P1022