THE INTERLEUKIN-12 SUBUNIT P40 SPECIFICALLY INHIBITS EFFECTS OF THE INTERLEUKIN-12 HETERODIMER

被引:280
作者
MATTNER, F [1 ]
FISCHER, S [1 ]
GUCKES, S [1 ]
JIN, SC [1 ]
KAULEN, H [1 ]
SCHMITT, E [1 ]
RUDE, E [1 ]
GERMANN, T [1 ]
机构
[1] MED KLIN 1,MAINZ,GERMANY
关键词
INTERLEUKIN-12; INTERLEUKIN-12 SUBUNIT P40; INHIBITION; T-HELPER CELLS OF TYPE-1; COSTIMULATOR;
D O I
10.1002/eji.1830230923
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The recently discovered cytokine interleukin (IL)-12 is a heterodimeric protein of two disulfide-bonded subunits of 35 and 40 kDa. IL-12 has multiple effects on T cells and natural killer (NK) cells. In particular it appears to be a major factor for the development of cellular immunity. So far activity of the single subunits alone has not been described, however their expression is regulated independently In this report we demonstrate for the first time that the mouse IL-12 subunit p40 (IL-12p40) specifically antagonizes the effects of the IL-12 heterodimer in different assay systems.The proliferation of mouse splenocytes activated by phorbol ester and IL-12 was inhibited by IL-12p40, whereas the proliferation induced by phorbol ester and IL-2 was not affected. Furthermore, the synthesis of interferon (IFN)-gamma by mouse splenocytes activated with IL-2 and IL-12 was suppressed by IL-12p40. Purified mouse splenic CD4+ T cells produced IFN-gamma upon activation with plate-bound anti-CD3 monoclonal antibody which was enhanced more than tenfold in the presence of IL-12. In this system IL-12p40 inhibited only the enhancement caused by IL-12 but not IFN-gamma synthesis of CD4+ T cells stimulated with anti-CD3 alone. Moreover, IL-12p40 inhibited the effects of IL-12 on differentiated T helper type 1 (T(h)1) cells. IFN-gamma production by T(h)1 cells induced in a T cell receptor-independent way by macrophages and IL-2 or macrophages and IL-12 was greatly reduced by IL-12p40 providing evidence for the endogenous synthesis of IL-12 in the T(h)1 cell, macrophage and IL-2 co-cultures. The specificity of inhibition was clearly demonstrated in the homotypic aggregation assay of T(h)1 cells. Incubation of T(h)1 cells with either IL-2 and IL-12 or IL-2 and tumor necrosis factor induces LFA-1/ICAM-1-dependent aggregation. Only IL-2 + IL-12 but not IL-2 + tumor necrosis factor-induced aggregation was inhibited in a dose-dependent manner by IL-12p40. Thus, the IL-12 subunit p40 appears to be a specific inhibitor for the IL-12 heterodimer.
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收藏
页码:2202 / 2208
页数:7
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