van den Berg A P, Twilhaar W N, van Son W J, van der Bij W, Klompmaker I J, Slooff M J, The T H, de Leij L H
Department of Gastroenterology and Hepatology, University Hospital, Groningen, The Netherlands.
Transpl Int. 1998;11 Suppl 1:S318-21. doi: 10.1007/s001470050487.
The availability of a method to measure the effects of drugs on immune reactivity should be helpful in optimizing treatment after organ transplantation. Since cyclosporine A (CSA) interferes with activation of T cells and cytokine synthesis, production of IL-2 and IFN-gamma might constitute a marker of this drug's effects. We measured the capacity for mitogen-stimulated production of these cytokines in whole blood by using immunostaining of intracellular and membrane antigens, followed by flow cytometry. The percentage of CD4+ T cells producing IL-2 or IFN-gamma was strongly reduced in 20 transplant patients compared with 24 healthy controls. The capacity for IL-2 production of CD4+ and CD8+ cells correlated inversely with CSA blood levels (P values 0.0087 and 0.0396, respectively). IFN-gamma production by CD4+ T cells showed a negative correlation with the prednisolone dose (P = 0.0175) and, for the CD8+ subset, with CSA trough levels (P = 0.0023). These data show that inhibition of T cell cytokine synthesis by CSA and prednisolone can be quantified.
一种测量药物对免疫反应性影响的方法的出现,应该有助于优化器官移植后的治疗。由于环孢素A(CSA)会干扰T细胞的激活和细胞因子的合成,白细胞介素-2(IL-2)和干扰素-γ(IFN-γ)的产生可能构成该药物作用的一个标志物。我们通过对细胞内和膜抗原进行免疫染色,然后进行流式细胞术,来测量全血中丝裂原刺激产生这些细胞因子的能力。与24名健康对照相比,20名移植患者中产生IL-2或IFN-γ的CD4+ T细胞百分比大幅降低。CD4+和CD8+细胞产生IL-2的能力与CSA血药浓度呈负相关(P值分别为0.0087和0.0396)。CD4+ T细胞产生IFN-γ与泼尼松龙剂量呈负相关(P = 0.0175),对于CD8+亚群,与CSA谷浓度呈负相关(P = 0.0023)。这些数据表明,CSA和泼尼松龙对T细胞细胞因子合成的抑制作用可以被量化。