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作 者:石裕明[1] 张立煌[1] 方海林[1] 何南祥[1] 刘克洲[1] 李敏伟[1] 姚航平[1]
机构地区:[1]浙江医科大学传染病研究所
出 处:《中华传染病杂志》1998年第3期144-147,共4页Chinese Journal of Infectious Diseases
基 金:国家自然科学基金;浙江省自然科学基金
摘 要:目的评价IL-4在重型肝炎治疗中的潜在应用价值。方法应用免疫组化法和半定量RT-PCR系统地观察IL-4对重型肝炎患者PBMCsIL-1α表达的影响。结果IL-4在蛋白质和mR-NA水平明显抑制LPS诱导的亚急性和慢性重型肝炎患者PBMCsIL-1α的产生,这种抑制作用呈剂量和时间依赖的方式。IL-4于100U/ml时开始出现抑制效应,于1000U/ml时抑制作用接近最大。虽然IL-4对慢性重型肝炎患者PBMCsIL-1α的抑制作用略低,但与未经IL-4处理的PBMCs相比较,IL-1α的表达水平仍明显下降。结论IL-4对亚急性和慢性重型肝炎PBMCsIL-1α的表达均具有较强的下向调节作用,在重型肝炎的治疗上可能具有潜在的应用价值,值得进一步研究。Objective To estimate the potential clinical value of IL 4 in the treatment of severe hepatitis. Methods In the present study, we observed the effect of IL 4 on expression of IL 1α in peripheral blood mononuclear cells (PBMCs) from patients with severe hepatitis at cellular and molecular levels using immunohistochemical assay and the technique of semiquantitative reverse transcriptional polymerase chain reaction (RT PCR).The isolated PBMCs were cultured in the presence of increasing concentration of IL 4 or IL 4 was added to cultures at different time courses after the challenge of LPS. Results It was found that IL 4 in dose and time dependent manner down regulated the LPS induced production of IL 1α in PBMCs from patients with severe hepatitis at the level of protein and mRNA. The inhibitory effect of IL 4 could be observed at the concentration of 100U/ml and nearly got to the climax at 1 000U/ml.Although the suppression of IL 4 on the production of IL 1α in PBMCs from chronic severe hepatitis was slightly weaker than on that from subacute severe hepatitis,there existed significant difference when compared with the control PBMCs untreated with IL 4. Conclusion
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