Different regulatory effects of pentoxifylline on human T cell activation pathways

被引:16
作者
Dong, RP
Umezawa, Y
Ikushima, H
Munakata, Y
Schlossman, SF
Morimoto, C
机构
[1] DANA FARBER CANC INST,DIV TUMOR IMMUNOL,BOSTON,MA 02115
[2] JUNTENDO UNIV,SCH MED,DEPT PATHOL 2,TOKYO 113,JAPAN
关键词
pentoxifylline; CD3; CD26; CD28; cytokine;
D O I
10.1023/A:1027362629161
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Pentoxifylline (PTX), a methylxanthine derivative, was examined for its effects on T cell proliferation and cytokine production stimulated by cross-linking anti-CD3 alone, anti-CD3 with PMA, anti-CD3 with anti-CD26, or anti-CDS with anti-CD28 mAb, respectively. PTX at a 3.5 x 10(-5) M concentration significantly inhibited T cell proliferation and the production of tumor necrosis factor-alpha, interleukin-2, and interleukin-4. Moreover, this effect was selective for stimulation by cross-linking anti-CD3 with PMA, or anti-CD3 with anti-CD26, but not by cross-linking anti-CDS with anti-CD28. These results suggest that the inhibitory effect of PTX on T cell activation involves the CD3 and CD26, but not the CD28 signal pathway.
引用
收藏
页码:247 / 252
页数:6
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