TYPE OF LYMPHOCYTES AFFECTED BY THE ISLET-ACTIVATING PROTEIN (IAP)

被引:1
作者
OHTA, Y
NAKAGAWA, Y
SAIJO, T
机构
[1] Biology Research Laboratories, Research and Development Division, Takeda Chemical Industries, Ltd., Yodogawa-ku, Osaka, 532, 17-85, Jusohonmachi
来源
IMMUNOPHARMACOLOGY | 1990年 / 19卷 / 03期
关键词
Cytokine; Flow cytometry; IAP; T lymphocyte;
D O I
10.1016/0162-3109(90)90069-Q
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
By flow cytometric analysis, we identified the subclass of lymphocytes that proliferates in response to islet-activating protein (IAP), both in vitro (human peripheral blood mononuclear cells, MNC, cultured with IAP) and in vivo (peripheral blood MNC derived from A/J mice treated with IAP). IAP caused a preferential proliferation of CD8+ T cells. These cells expressed the IL-2 receptors on their surface. CD4+ CD8+ T cells could also be detected in these cultures. IAP caused human MNC to produce IL-1 and to induce expression of HLA-DR antigen. These effects may play an important role in the T-cell proliferation induced by IAP, although IAP by itself suppressed the proliferative action of IL-1 in mouse thymocytes. IAP induced proliferation of the purified CD4+ cells but had a smaller effect on the purified CD8+ cells. This suggests that the proliferation of CD8+ cells in IAP-treated MNC depends on the function of other types of cell, e.g. CD4+ cell and macrophage. © 1990.
引用
收藏
页码:197 / 205
页数:9
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