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乙肝核酸疫苗接种小鼠后特异性抗原表达及CTL应答的动态观察 被引量:1

The Serial Observation of Specific Antigen Expression and CTL Responses Induced by A Hepatitis B Virus DNA Vaccine in BALB/c Mice
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摘要 目的:观察乙肝病毒(hepatitis B virus,HBV)核酸疫苗pCMV-S2S免疫小鼠后,接种局部HBV preS2S抗原的表达及特异性细胞毒性T淋巴细胞(CTL)应答的动态变化。方法:将pCMV-S2S接种到BALB/c小鼠胫前肌,分别以免疫组化法检测接种局部肌肉HBV preS2S抗原表达的动态变化,乳酸脱氢酶(LDH)释放法检测特异性CTL活性的动态变化。结果:小鼠接种pCMV-S2S后,局部肌肉细胞3d后已有少量目的抗原HBV preS2S蛋白表达,4周时表达最强,至6月时仍可检出有preS2S蛋白表达,但表达强度明显减弱。小鼠接种pCMV-S2S3天后,特异性CTL活性平均值最高为21·67%,12周时CTL活性平均值最高为35·14%,6月时仍可检出较弱的CTL活性。结论:HBV核酸疫苗pCMV-S2S能在小鼠体内持续表达特异性抗原及诱生特异性CTL应答。 Objective:To observe the dynamic changes of specific antigen expression and cytotoxicity T lymphocyte (CTL) responses induced by a hepatitis B virus DNA vaccine pCMV-S2S in BALB/c mice.Methods:BALB/c mice were intramuscularly injected with pCMV-S2S.The expression of HBV specific antigen preS2S in the muscles were detected by immunohistochemistry assays.The specific CTL activities induced by mice were measured by lactate dehydrogenase (LDH) release assays.Results:HBV preS2S antigen expression in the mice muscles was detected 3 days after the injection of pCMV-S2S,increased to the peak 4 weeks after injection,and still could be detected 6 months later with weaker expression.Relative lower level of HBV preS2S-specific CTL lysis activities in pCMV-S2S mice was detected 3 days after injection.The average HBV preS2S-specific CTL lysis values achieved the peak by 35.14% 12 weeks after injection,and still kept at low level 6 months after injection.Conclusion:The hepatitis B virus DNA vaccine pCMV-S2S vaccination may elicit substantial HBV preS2S expression and HBV preS2S-specific CTL responses in vivo,and lasted for a relatively long time.
出处 《华西医学》 CAS 2008年第3期565-567,共3页 West China Medical Journal
基金 国家自然科学基金(No.30571640) 国家863高技术项目(No.2002AA214161) 四川省应用基础研究项目(No.04JY029-002-7)
关键词 乙型肝炎病毒 前S2S抗原 核酸疫苗 抗原表达 细胞毒性T淋巴细胞 hepatitis B virus,preS2S antigen,DNA vaccine,antigen expression,cytotoxicity T lymphocyte
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  • 1Guidotti LG. The role of cytotoxic T cells and cytokines in the control of hepatitis B virus infection [ J ]. Vaccine, 21XI2, Suppl 4: A80 - 82.
  • 2Sing GK, Ladhams A,Amold S, et al. A longitudinal analysis of cytotoxic T lymphocyte precursor frequencies to the hepatitis B virus in chronically infected patients [J]. J Viral Hepat, 2001, 8 (1): 19-29.
  • 3Chisari FV, Ferrai C. Cytotoxic T cells and viral hepatitis [ J ]. J Clin Invest, 1997, 99 (7) : 1472 - 1477.
  • 4Yah J,Liu X,Wang Y, et al. Enhancing the potency of HBV DNA vaccines using fusion genes of HBV - specific antigens and the N - terminal fragment of gp96[ J]. J Gene Med, 2007, 9 (2): 107-121.
  • 5Iuxembourg A, Hannaman D, EUefsen B, et al. Enhancement of immune responses to an HBV DNA vaccine by electroporation [ J ]. Vaccine, 2006, 24 (21): 4490-4493.
  • 6Huang Y, Chen Z,Jia H, et al. Induction of Tcl response and enhanced cytotoxic T lymphocyte activity in mice by dendritic cells transduced with adenovims expressing HBsAg [J]. Clin Immunol, 2006, 119 (3): 280-290.
  • 7Fissolo N, Riedl P, Reimann J, et al. DNA vaccines prime CD8 + T cell responses to epitopes of viral antigens produced from overlapping reading frames of a single coding sequence [J]. Eur J Immunol, 2005, 35 (1): 117-127.
  • 8秦山,唐红,赵连三,刘丽,林勇.乙肝基因疫苗系列质粒的构建及其在真核细胞中的表达[J].华西医科大学学报,2001,32(2):172-174. 被引量:5
  • 9何芳,秦山,赵连三,刘丽.乙型肝炎病毒表面抗原M蛋白真核表达细胞株的建立及其表达产物的检测[J].中国免疫学杂志,2001,17(5):236-238. 被引量:4
  • 10Encke J,zu Putlitz J,Wands JR. DNA Vaccine [J]. Intervirology, 1999, 42: 117 - 124.

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