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Generation of alloreactive cytolytic T lymphocytes by immobilized anti-CD3 monoclonal antibodies. Analysis of requirements for human cytolytic T-lymphocyte differentiation.

机译:固定化抗CD3单克隆抗体产生同种反应性溶细胞性T淋巴细胞。分析人类溶细胞性T淋巴细胞的需求。

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摘要

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.
机译:在无单核细胞的T细胞活化系统中研究了诱导人溶细胞性T淋巴细胞(CTL)活性的要求,该系统使用固定化的抗CD3单克隆抗体(mAb)作为刺激。对HLA-A和-B基因座抗原具有特异性的同种异体反应性CTL可以在激活开始后的两天内证明。通过添加单核细胞或外源性细胞因子并不能增强由最佳浓度的固定化抗CD3 mAb引发的纯化T细胞中CTL的诱导,而添加抗CD25 mAb则在很大程度上阻止了反应。在抗CD3 mAb刺激最差后,添加重组白介素(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。最后表明,固定化的抗CD3 mAb在纯化的CD4 +和CD8 +细胞中均诱导显着水平的CTL活性。这项研究表明,在CTL前体分化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。

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