De Jong R, Brouwer M, Rebel V I, Van Seventer G A, Miedema F, Van Lier R A
Central Laboratory of The Netherlands Red Cross Blood Transfusion Service, University of Amsterdam.
Immunology. 1990 Jul;70(3):357-64.
Requirements for the induction of human cytolytic T-lymphocyte (CTL) activity were studied in a monocyte-free T-cell activation system that uses immobilized anti-CD3 monoclonal antibodies (mAb) as a stimulus. Alloreactive CTL with specificity for HLA-A and -B locus antigens could be demonstrated within 2 days after the initiation of activation. CTL induction in purified T cells initiated by an optimal concentration of immobilized anti-CD3 mAb was not enhanced by the addition of monocytes or exogeneous cytokines, whereas addition of anti-CD25 mAb largely blocked the response. Upon suboptimal anti-CD3 mAb stimulation, addition of recombinant interleukin (rIL)-2, rIL-1 and rIL-4, but not recombinant interferon-gamma (IFN-gamma) or rIL-6, potentiated the development of CTL activity. Finally it was shown that immobilized anti-CD3 mAb induced significant levels of CTL activity in both purified CD4+ and CD8+ cells. This study indicates that the requirement for cytokines in the differentiation of CTL precursors depends on the strength of the activation signal delivered through the T-cell receptor.
在一个无单核细胞的T细胞激活系统中,研究了诱导人细胞溶解性T淋巴细胞(CTL)活性的条件,该系统使用固定化抗CD3单克隆抗体(mAb)作为刺激物。在激活开始后2天内即可证明对HLA - A和 - B位点抗原具有特异性的同种反应性CTL。由最佳浓度的固定化抗CD3 mAb启动的纯化T细胞中的CTL诱导,不会因添加单核细胞或外源性细胞因子而增强,而添加抗CD25 mAb则在很大程度上阻断了反应。在次优抗CD3 mAb刺激下,添加重组白细胞介素(rIL)-2、rIL - 1和rIL - 4,但不添加重组干扰素 - γ(IFN - γ)或rIL - 6,可增强CTL活性的发展。最后表明,固定化抗CD3 mAb在纯化的CD4 +和CD8 +细胞中均诱导出显著水平的CTL活性。这项研究表明,CTL前体分化过程中对细胞因子的需求取决于通过T细胞受体传递的激活信号的强度。