Górski A, Grieb P, Korczak-Kowalska G, Wierzbicki P, Stepień-Sopniewska B, Mrowiec T
Department of Immunology, Warsaw Medical School, Poland.
Immunopharmacology. 1993 Nov-Dec;26(3):197-202. doi: 10.1016/0162-3109(93)90035-o.
We have previously shown that the novel immunosuppressive agent cladribine (CDA) inhibits human T and B cell lymphoproliferative responses and immunoglobulin synthesis in vitro, yet appears to be particularly efficacious as an inhibitor of B cell responses. We now report the effects of CDA on the human mixed lymphocyte reaction and on expression of T and B cell activation markers. CDA produced a significant inhibition of lymphocyte proliferation in human mixed lymphocyte reactions at a concentration of 10 nM. At concentrations of 10-100 nM the drug inhibited phytohaemagglutinin-induced expression of CD25 and HLA-D (by approximately 50%), but not phorbol myristate acetate-induced expression of CD69 on purified human T cells. At a concentration of 10 nM CDA totally abolished Staphylococcus aureus Cowan-induced expression of CD25 on purified B cells. These findings confirm that CDA is a potent immunosuppressive agent with some selectivity towards B cells. The drug may have potentially wide applications in clinical immunosuppression.
我们之前已经表明,新型免疫抑制剂克拉屈滨(CDA)在体外可抑制人T和B细胞的淋巴细胞增殖反应以及免疫球蛋白合成,但作为B细胞反应的抑制剂似乎特别有效。我们现在报告CDA对人混合淋巴细胞反应以及T和B细胞活化标志物表达的影响。在浓度为10 nM时,CDA对人混合淋巴细胞反应中的淋巴细胞增殖产生了显著抑制作用。在10 - 100 nM的浓度下,该药物抑制了植物血凝素诱导的CD25和HLA - D的表达(约50%),但对纯化的人T细胞上佛波酯诱导的CD69表达没有抑制作用。在浓度为10 nM时,CDA完全消除了金黄色葡萄球菌Cowan诱导的纯化B细胞上CD25的表达。这些发现证实CDA是一种强效免疫抑制剂,对B细胞具有一定的选择性。该药物在临床免疫抑制中可能具有广泛的应用潜力。