Alsinet E, Inglés-Esteve J, Vilella R, Lozano F, Milá J, Rojo I, Martorell J, Vives J, Gayá A
Servei d'Immunología, Hospital Clínic i Provincial, Barcelona, Spain.
Eur J Immunol. 1990 Dec;20(12):2801-4. doi: 10.1002/eji.1830201240.
We have generated seven monoclonal antibodies (mAb) that recognize the T200 molecule. These mAb have been classified by competitive binding assay in flow cytometry into three groups each reacting with a different epitope of the T200 molecule: (a) 136-4B5, that shows a sialic acid nature, (b) 135-4H9, 135-4C5, 144-2, 155-2 and (c) 72-5D3, 124-2H12b. A heterogeneous effect was observed when they were tested on an anti-immunoglobulin-induced B cell proliferation. Whereas 72-5D3 and 135-4H9 mAb inhibited the proliferative response of B cells, 136-4B5 mAb greatly enhanced it, both effects being dose dependent. We can conclude that anti-CD45 mAb have a different and contrary functional behavior on anti-Ig-induced B cell proliferation, depending on the epitope recognized. The basis for such a difference could reside in the glucidic nature of the epitope recognized by the 136-4B5 mAb.
我们已经制备了七种识别T200分子的单克隆抗体(mAb)。通过流式细胞术中的竞争性结合试验,这些单克隆抗体被分为三组,每组与T200分子的不同表位发生反应:(a)136 - 4B5,显示出唾液酸性质;(b)135 - 4H9、135 - 4C5、144 - 2、155 - 2;(c)72 - 5D3、124 - 2H12b。当用它们检测抗免疫球蛋白诱导的B细胞增殖时,观察到了异质性效应。72 - 5D3和135 - 4H9单克隆抗体抑制B细胞的增殖反应,而136 - 4B5单克隆抗体则显著增强该反应,两种效应均呈剂量依赖性。我们可以得出结论,抗CD45单克隆抗体在抗Ig诱导的B细胞增殖上具有不同且相反的功能行为,这取决于所识别的表位。这种差异的基础可能在于136 - 4B5单克隆抗体所识别表位的糖性质。