Moretta A, Accolla R S, Cerottini J C
J Exp Med. 1982 Feb 1;155(2):599-604. doi: 10.1084/jem.155.2.599.
We have studied the effect on the interleukin (IL-) 2-dependent human T cell growth of two distinct monoclonal antibodies (Mab), D1-12 and 4F2, with specificity for common determinant of human Ia antigens and for a differentiation antigen expressed on all activated T cells, respectively. Strong inhibition of cell growth was found in cultures supplemented with the anti-Ia D1-12 Mab but not in cultures supplemented with 4F2 Mab. These results were obtained when either total mixed leukocyte culture (MLC) T cells or an MLC-derived T cell clone were used as indicator cell systems for IL-2 activity. The inhibition of cell growth appears to be mediated by a direct interaction of D1-12 Mab with the cells and not by a direct inactivation of the growth factor, as addition of the antibody to murine MLC T cells, which do not express the determinant defined by D1-12 Mab, resulted in no inhibition of their proliferation induced by the same source of human IL-2.
我们研究了两种不同的单克隆抗体(Mab),即D1-12和4F2,分别对人白细胞介素(IL-)2依赖性人T细胞生长的影响,D1-12对人Ia抗原的共同决定簇具有特异性,4F2对所有活化T细胞上表达的一种分化抗原具有特异性。在添加抗Ia D1-12 Mab的培养物中发现细胞生长受到强烈抑制,而在添加4F2 Mab的培养物中未发现这种抑制。当使用全混合淋巴细胞培养(MLC)T细胞或MLC衍生的T细胞克隆作为IL-2活性的指示细胞系统时,获得了这些结果。细胞生长的抑制似乎是由D1-12 Mab与细胞的直接相互作用介导的,而不是由生长因子的直接失活介导的,因为将该抗体添加到不表达D1-12 Mab所定义决定簇的鼠MLC T细胞中,并未抑制由相同来源的人IL-2诱导的它们的增殖。