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作 者:李宁[1] 范学工[2] 朱才[2] 应若素[2] 黄燕[2]
机构地区:[1]中南大学湘雅医院输血科,长沙410008 [2]中南大学湘雅医院感染病科,长沙410008
出 处:《免疫学杂志》2007年第5期506-509,共4页Immunological Journal
基 金:湖南省科技攻关计划项目资助课题(04SK3040-3);长沙市科技项目(K05ST002-12)
摘 要:目的观察CpG-ODN体外对慢性乙型肝炎患者PBMC的免疫刺激效应。方法CpG-ODN体外刺激慢性乙肝患者外周血单个核细胞(PBMC),用ELISA检测培养液中IFN-α的水平;将不同比例的PBMC培养上清与HepG2.2.15细胞共孵育4和8d后,用ELISA和荧光定量PCR法,分别检测培养上清液中HBsAg、HBeAg和HBV DNA的水平;MTT法观察活化的PBMC培养上清液对HepG2.2.15的杀伤作用。结果CpG-ODN可有效诱导慢性乙肝患者PBMC分泌IFN-α,增强其活化的PBMC培养上清液对HepG2.2.15的杀伤作用;CpG-ODN本身虽不能直接抑制HBV的复制,但可通过其活化的PBMC的培养上清抑制HepG2.2.15细胞产生HBsAg、HBeAg和HBV DNA。结论CpG-ODN可有效激活慢性乙肝患者的免疫细胞,发挥抗病毒效应。Objective To investigate the effects of synthetic oligodeoxynucleotides (ODN) containing unmethylated CpG dinucleotides (CpG-ODN) on enhancing immune response in PBMCs of patients infected with hepatitis B virus (HBV). Methods CpG-ODN was co-cultured with peripheral blood mononuclear cells (PBMCs) obtained from healthy controls and individuals infected with HBV, and the levels of IFN-α in the culture supernatants were measured by ELISA. The culture supernatants of PBMCs were added to HBV-transfected HepG2.2.15 cells with various ratios. Levels of HBsAg, HBeAg, and HBV DNA in culture supernatant of HepG2.2.15 cells were detected by ELISA and fluorescence quantitative PCR at day 4 and 8. MTT method was used to detect lytic activity of HepG2.2.15 cells mediated by the culture supernatants of CpG-ODN-stimulated PBMCs. Results CpG-ODN induced high amounts of IFN-α production. The lysis of HepG2.2.15 cells mediated by the culture supernatants of CpG-ODN-stimulated PBMC was increased. CpG-ODN alone could not inhibit HBV replication directly, but the culture supernatant of PMBCs activated with CpG-ODN could remarkably inhibit the production of HBsAg, HBeAg and HBV DNA by HepG2.2.15 cells. Conclusion CpG-ODN can efficiently increase the immune response of chronic hepatitis B patients and enhance the antiHBV effects.
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