Balow J E, Hurley D L, Fauci A S
J Immunol. 1975 Mar;114(3):1072-6.
The effects of acute vs. chronic glucocorticosteroid administration on established cellular immune responses were studied in guinea pigs previously sensitized to tuberculin. A greater than 50% reduction in circulating lymphocytes was observed 4 hr after injection of soluble hydrocortisone and 24 hr after daily subcutaneous injections of depot cortisone acetate. After a single dose of hydrocortisone, peripheral lymphocyte migration inhibitory factor (MIF) production and antigen and mitogen-induced proliferation were unchanged. However, the peripheral lymphocytes remaining in the circulation after chronic cortisone treatment showed a marked decrease in both antigen-induced MIF and proliferation, although mitogen responses remained normal. Although similar levels of lymphocytopenia were induced by acute and chronic glucocorticosteroid administration, only chronic treatment was associated with depression of certain cell-mediated lymphocyte functions. The available evidence suggests that these changes may depend on GCS-induced selective alterations in the circulation patterns of certain subpopulations of lymphocytes.
在先前已对结核菌素致敏的豚鼠中,研究了急性与慢性给予糖皮质激素对已建立的细胞免疫反应的影响。注射可溶性氢化可的松4小时后以及每日皮下注射醋酸长效可的松24小时后,观察到循环淋巴细胞减少超过50%。单次给予氢化可的松后,外周淋巴细胞迁移抑制因子(MIF)的产生以及抗原和丝裂原诱导的增殖均未改变。然而,慢性可的松治疗后仍留在循环中的外周淋巴细胞,其抗原诱导的MIF和增殖均显著降低,尽管丝裂原反应仍正常。虽然急性和慢性给予糖皮质激素均可诱导相似程度的淋巴细胞减少,但只有慢性治疗与某些细胞介导的淋巴细胞功能受抑制有关。现有证据表明,这些变化可能取决于糖皮质激素诱导的某些淋巴细胞亚群循环模式的选择性改变。