Oh-Ishi T, Goldman C K, Misiti J, Waldmann T A
Metabolism Branch, National Cancer Institute, Bethesda, MD 20892.
Proc Natl Acad Sci U S A. 1988 Sep;85(17):6478-82. doi: 10.1073/pnas.85.17.6478.
The role of interleukin 2 (IL-2) in the activation of suppressor T cells was investigated by using the monoclonal antibody anti-Tac, which blocks the binding of IL-2 to the 55-kDa peptide of the high-affinity IL-2 receptor. Anti-Tac was added to an antigen-nonspecific suppressor system in which Con A-induced suppressor T cells were generated during a preculture period, and their effects on immunoglobulin production were assessed in second, indicator cultures containing pokeweed mitogen and peripheral blood mononuclear cells. Anti-Tac added during the preculture period inhibited Con A-induced suppressor T-cell generation. Cells activated by a short (2-day) preculture period to become effectors of suppression were primarily of the Tac-positive, T8 (CD8)-positive phenotype. Tac-positive, T8-negative T cells might also contribute to the suppressor activity. Our studies indicate that anti-Tac, by producing a functional blockade of human high-affinity IL-2 receptors, inhibits the generation of antigen-nonspecific suppressor T cells.
通过使用抗 Tac 单克隆抗体研究白细胞介素 2(IL-2)在抑制性 T 细胞激活中的作用,该抗体可阻断 IL-2 与高亲和力 IL-2 受体的 55kDa 肽的结合。将抗 Tac 添加到抗原非特异性抑制系统中,在预培养期产生刀豆蛋白 A 诱导的抑制性 T 细胞,并在含有商陆有丝分裂原和外周血单核细胞的第二个指示培养物中评估其对免疫球蛋白产生的影响。预培养期添加的抗 Tac 抑制了刀豆蛋白 A 诱导的抑制性 T 细胞的产生。通过短(2 天)预培养期激活成为抑制效应细胞的细胞主要是 Tac 阳性、T8(CD8)阳性表型。Tac 阳性、T8 阴性 T 细胞也可能有助于抑制活性。我们的研究表明,抗 Tac 通过对人高亲和力 IL-2 受体产生功能性阻断,抑制了抗原非特异性抑制性 T 细胞的产生。