强的松龙与甲基强的松龙对类风湿关节炎淋巴细胞抑制效能的比较研究

Toshihiko Hirano , Norioki Tsuboi , Masato Homma , Kitaro Oka , Tohru Takekoshi , Koichiro Tahara , Hirofumi Takanashi , Haruo Abe , Yukitomo Urata , Tohru Hayashi
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引用次数: 12

摘要

我们比较了强的松龙和甲基强的松龙对类风湿关节炎(RA)的淋巴细胞抑制作用。在体外测定了44例RA患者和30例健康人外周血单个核细胞(PBMCs)诱导的糖皮质激素(GCs)的ic50,并评价了两种GCs的ic50差异。强的松龙和甲基强的松龙对类风湿关节炎pbmc -胚发生的平均ic50(±SD)分别为17.2±17.1和12.6±18.4 ng/ml,强的松龙ic50与甲基强的松龙ic50无显著差异。强的松龙和甲基强的松龙对健康pbmc的平均ic50分别为19.4±22.4和3.7±3.9 ng/ml,甲强的松龙的效价明显高于强的松龙(p<0.01)。在类风湿因子(RF)水平高(20 IU/ml)和类风湿关节炎颗粒凝集值(RAPA)水平(80)的RA患者中,甲基强的松龙对PBMCs的效价显著高于类风湿因子或RAPA水平低的患者(p < 0.05)。然而,在强的松龙ic50中,两个患者亚组之间没有观察到这种差异。与已报道的肾移植病例和健康受试者不同,强的松龙和甲基强的松龙对ra - pbmc的淋巴细胞抑制作用没有差异。然而,表现出高水平RF或RAPA的RA患者的pbmc对甲基强的松龙比强的松龙更敏感。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative study of lymphocyte-suppressive potency between prednisolone and methylprednisolone in rheumatoid arthritis

We compared lymphocyte-suppressive potencies of prednisolone and methylprednisolone in rheumatoid arthritis (RA). IC50s of the glucocorticoids (GCs) on concanavalin A-induced blastogenesis of peripheral-blood mononuclear cells (PBMCs) from 44 RA patients and 30 healthy subjects were estimated in vitro, and differences in the IC50s of the two GCs were evaluated. The mean (±SD) IC50s for prednisolone and methylprednisolone on PBMC-blastogenesis of RA were 17.2±17.1 and 12.6±18.4 ng/ml, respectively, and no significant differences were observed between prednisolone-IC50 and methylprednisolone-IC50. In contrast, the mean IC50s of prednisolone and methylprednisolone on healthy PBMCs were 19.4±22.4 and 3.7±3.9 ng/ml, respectively, and thus methylprednisolone potency was significantly higher than prednisolone potency (p<0.01). Methylprednisolone potency against PBMCs in RA patients exhibiting a high level of rheumatoid factor (RF) (>20 IU/ml) and the rheumatoid arthritis particle-agglutination value (RAPA) (>80) was significantly higher than that of patients exhibiting a lower level of RF or RAPA (p<0.05). In prednisolone-IC50, however, such differences between the two patient-subgroups were not observed. Unlike reported cases of renal transplantation and healthy subjects, there was no difference in the lymphocyte-suppressive potencies for both prednisolone and methylprednisolone on RA-PBMCs. However, PBMCs from RA patients exhibiting high levels of RF or RAPA are more sensitive to methylprednisolone rather than prednisolone.

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