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丙型肝炎高变区1合成肽体外刺激HCV感染PBMC细胞因子分泌的研究 被引量:3

Cytokines secretion by peripheral blood mononuclear cells from hepatitis C patients after stimulation with synthetic peptides at the highly variable region
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摘要 目的检测丙型肝炎病毒(HCV)高变区1(HVR1)模拟表位刺激自然感染患者外周血淋巴细胞后的细胞因子水平变化。方法细胞因子检测运用ELISA、流式细胞仪(FACS)淋巴细胞分类以及计算机模拟多肽抗原性。结果(1)1号和5号合成肽刺激HCV患者外周血单核细胞(PBMC)后,患者PBMC出现了明显的增殖;(2)培养上清中干扰素γ(IFNγ)、白介素4(IL-4)、白介素10(IL-10)都有不同程度的提高,白介素2(IL-2)和肿瘤坏死因子α(TNF-α)的水平并没有提高;(3)增殖细胞主要为CD4阳性淋巴细胞。结论我们设计的HCV高变区1合成肽引发的免疫因子的释放倾向于TH2类因子。 Objective Test the cytokines secretion by peripheral blood mononuclear cells (PBMC) from hepatitis C patients after stimulation with highly variable region ( HVR1 ) synthetic peptides. Methods ELISA was used to test the cytokines secretion, flow cytometry to group the proliferated cells, and the antigencity of synthetic peptide was predicted by the computer modeling. Results ( 1 ) There were PBMC proliferation when stimulated by HVR1 antigen synthetic peptides. (2) There was a rise of IFN-γ, IL-4 and IL-10. But no rise of IL-2 and TNF-γ, was found. (3) The proliferated cells were mainly CD4 ^+ lymphocytes. Conclusion PMBC from hepatitis C patients tend to secret Th2 cytokines after stimulation with HVR1 designed by the authors.
出处 《中华实验和临床病毒学杂志》 CAS CSCD 北大核心 2005年第3期279-281,共3页 Chinese Journal of Experimental and Clinical Virology
基金 全军95重点课题基金资助(96M174 98z089)
关键词 肝炎病毒属 肽合成 表位 细胞因子类 单核细胞/血液 丙型肝炎病毒(HCV) 细胞因子分泌 HCV感染 高变区1 PBMC Hepatitis viruses Peptide synthesis Epitopes Cytokines Monoeytes/blood
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  • 1赵军,程云,苏琴,李静,段学章,刘茂昌,何江英,曹阳,付体权.20例中国人HCVⅡ/1b型高变区1序列变异的动态观察[J].中华微生物学和免疫学杂志,2000,20(6):507-510. 被引量:10
  • 2Eckels DD, Flomenberg P, Gill. Hepatitis C virus: models of immunopathogenesis and prophylaxis. Transfusion, 1996, 36: 836-844.
  • 3Zignego AL , Macchia D, Monti M. Infection of peripheral blood mononuclear cells by infected patients. J Hepatol, 1992,15: 382-386.
  • 4Bouffard P, Hayashi PH, Acevedo R, et al. Hepatitis C virus is detected in a monocyte/macrophage subpopulation of peripheral blood mononuclear cells of infected patients. J Infect Dis, 1992, 166:1276-1280.
  • 5Ikeda M, Kate N, Mizutani T, et al. Analysis of the cell tropism of HCV by using in vitro HCV-infected human lymphocytes and hepatocytes. J Hepatol, 1997,27:445-454.

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