Fauci A S
Clin Exp Immunol. 1976 Apr;24(1):54-62.
The present study was undertaken to determine what, if any, differential effect various commonly used corticosteroid preparations had on the numbers and specific functions of lymphocyte subpopulations when these agents were administered in equivalent pharmacological dosages. Normal volunteers received a single dose of either 320 mg of hydrocortisone intravenously, 80 mg of prednisone orally, or 12 mg of dexamethasone orally. There was a marked lymphocytopenia and monocytopenia maximal 4-6 hr following administration of all three corticosteroid preparations with almost identical kinetics and degree of fall in total cell numbers as well as proportions of thymus-derived and bone marrow-derived lymphocytes. Hydrocortisone and prednisone caused only a slight suppression of phytohaemagglutiinin (PHA) induced lymphocyte blastogensis which could be reversed at supra-optimal concentrations of PHA. On the contrary, dexamethasone administration casued a marked suppression of PHA responses which was not reversed by supra-optimal PHA stimulation. In addition, hydrocortisone and prednisone administration did not suppress non-specific PHA-induced cellular cytotoxcity, while dexamethasone caused a marked suppression (P less than 0.001) of cytotoxicity. These studies show that although equivalent anti-inflammatory doses of these three corticosteroid preparations cause almost identical suppression of the numbers of circulating lymphocyte populations, they have a differential effect of the numbers of circulating lymphocyte populations, they have a differential effect on a certain in vitro functional correlates of cell-mediated immunity.
本研究旨在确定当以等效药理剂量给予各种常用皮质类固醇制剂时,它们对淋巴细胞亚群的数量和特定功能是否有差异效应。正常志愿者静脉注射320mg氢化可的松、口服80mg泼尼松或口服12mg地塞米松单剂量。在给予所有三种皮质类固醇制剂后4 - 6小时出现明显的淋巴细胞减少和单核细胞减少,总细胞数以及胸腺来源和骨髓来源淋巴细胞比例的下降动力学和程度几乎相同。氢化可的松和泼尼松仅引起植物血凝素(PHA)诱导的淋巴细胞增殖轻微抑制,在PHA超最佳浓度时可逆转。相反,给予地塞米松导致PHA反应明显抑制,超最佳PHA刺激不能逆转。此外,给予氢化可的松和泼尼松不抑制非特异性PHA诱导的细胞毒性,而地塞米松导致细胞毒性明显抑制(P小于0.001)。这些研究表明,尽管这三种皮质类固醇制剂的等效抗炎剂量对循环淋巴细胞群体数量的抑制几乎相同,但它们对细胞介导免疫的某些体外功能相关性有差异效应。