Nair M P, Schwartz S A
J Immunol. 1984 Jun;132(6):2876-82.
The in vitro effect of prednisolone (PRD) on NK and ADCC activities of human lymphocytes was investigated. PRD at concentrations ranging from 7.5 X 10(-3) to 1 X 10(-5) M significantly inhibited NK activity, while concentrations of 7.5 X 10(-3) to 1 X 10(-4) M inhibited ADCC activities of PBL when added directly to the mixture of effector and target cells. Lymphocytes pre-cultured for 24 hr with PRD at concentrations ranging from 1 X 10(-4) M to 1 X 10(-6) M showed significant suppression of their NK activity. Inhibition was proportional to the concentration of the drug, and was observed at as early as 1 hr of incubation at various effector to target cell ratios with several targets. PRD also inhibited NK and ADCC activities of purified T cells, non-T cells, and NK-enriched effector cells. In target-binding assays, PRD decreased the target-binding capacity of effector lymphocytes in a dose-dependent manner. PRD-induced inhibition could be reversed by incubating lymphocytes for 1 hr with interferon or IL 2. Pretreatment of targets with PRD for 4 hr did not affect cytotoxic activity. Inhibition of cytotoxicity was not due to direct toxicity to effector cells because lymphocytes treated with PRD showed normal spontaneous 51Cr release, and their viability after 24 hr of pre-culture with PRD was comparable to that of untreated control cells. These results demonstrate that PRD has significant immunomodulatory effects on human NK and ADCC activities that may be of clinical relevance.
研究了泼尼松龙(PRD)对人淋巴细胞自然杀伤(NK)活性和抗体依赖的细胞介导的细胞毒性(ADCC)活性的体外作用。浓度范围为7.5×10⁻³至1×10⁻⁵M的PRD显著抑制NK活性,而当直接添加到效应细胞和靶细胞混合物中时,浓度为7.5×10⁻³至1×10⁻⁴M的PRD抑制外周血淋巴细胞(PBL)的ADCC活性。用浓度范围为1×10⁻⁴M至1×10⁻⁶M的PRD预培养24小时的淋巴细胞显示其NK活性受到显著抑制。抑制作用与药物浓度成正比,并且在与多个靶细胞以不同效应细胞与靶细胞比例孵育1小时时就可观察到。PRD还抑制纯化的T细胞、非T细胞和富含NK的效应细胞的NK和ADCC活性。在靶细胞结合试验中,PRD以剂量依赖的方式降低效应淋巴细胞的靶细胞结合能力。用干扰素或白细胞介素2孵育淋巴细胞1小时可逆转PRD诱导的抑制作用。用PRD预处理靶细胞4小时不影响细胞毒性活性。细胞毒性的抑制不是由于对效应细胞的直接毒性,因为用PRD处理的淋巴细胞显示正常的自发⁵¹Cr释放,并且在与PRD预培养24小时后的活力与未处理的对照细胞相当。这些结果表明,PRD对人NK和ADCC活性具有显著的免疫调节作用,这可能具有临床相关性。