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标题: DNA Prime-Adenovirus Boost Immunization Induces a Vigorous and Multifunctional T [打印本页]

作者: StephenW    时间: 2012-8-10 14:35     标题: DNA Prime-Adenovirus Boost Immunization Induces a Vigorous and Multifunctional T

本帖最后由 StephenW 于 2012-8-10 14:36 编辑

http://jvi.asm.org/content/86/17/9297.abstract?etoc
DNA Prime-Adenovirus Boost Immunization Induces a Vigorous and Multifunctional T-Cell Response against Hepadnaviral Proteins in the Mouse and Woodchuck Model

    Anna D. Kosinska a,
    Lena Johrden b,
    Ejuan Zhang a, c,
    Melanie Fiedler a,
    Anja Mayer a,
    Oliver Wildner b,d,
    Mengji Lu a and
    Michael Roggendorf a

- Author Affiliations

    a Institute of Virology, University Hospital of Essen, Essen, Germany
    b Department of Molecular and Medical Virology, Institute of Microbiology and Hygiene, Ruhr University Bochum, Bochum, Germany
    c Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, People's Republic of China
    d Paul Ehrlich Institute, Division of Medical Biotechnology, Langen, Germany

ABSTRACT

Induction of hepatitis B virus (HBV)-specific cytotoxic T cells by therapeutic immunization may be a strategy to treat chronic hepatitis B. In the HBV animal model, woodchucks, the application of DNA vaccine expressing woodchuck hepatitis virus (WHV) core antigen (WHcAg) in combination with antivirals led to the prolonged control of viral replication. However, it became clear that the use of more potent vaccines is required to overcome WHV persistence. Therefore, we asked whether stronger and more functional T-cell responses could be achieved using the modified vaccines and an optimized prime-boost vaccination regimen. We developed a new DNA plasmid (pCGWHc) and recombinant adenoviruses (AdVs) showing high expression levels of WHcAg. Mice vaccinated with the improved plasmid pCGWHc elicited a stronger WHcAg-specific CD8+ T-cell response than with the previously used vaccines. Using multicolor flow cytometry and an in vivo cytotoxicity assay, we showed that immunization in a DNA prime-AdV boost regimen resulted in an even more vigorous and functional T-cell response than immunization with the new plasmid alone. Immunization of naïve woodchucks with pCGWHc plasmid or AdVs induced a significant WHcAg-specific degranulation response prior to the challenge, this response had not been previously detected. Consistently, this response led to a rapid control of infection after the challenge. Our results demonstrate that high antigen expression levels and the DNA prime-AdV boost immunization improved the T-cell response in mice and induced significant T-cell responses in woodchucks. Therefore, this new vaccination strategy may be a candidate for a therapeutic vaccine against chronic HBV infection.
FOOTNOTES

        Received 28 February 2012.
        Accepted 11 June 2012.
    Address correspondence to Michael Roggendorf, [email protected].


作者: StephenW    时间: 2012-8-10 14:35

DNA总理腺病毒的升压免疫诱导针对嗜肝病毒蛋白质的蓬勃和多功能的T细胞在老鼠和土拨鼠模型的响应

    安娜四Kosinska 1,
    莱娜Johrden B,
    ejuan张A,C,
    梅拉妮菲德勒A,
    安雅·迈耶A,
    奥利弗·威尔德纳B,D,
    孟继良鲁A和
    迈克尔Roggendorfà

- 作者背景

    一个病毒学研究所,埃森,德国埃森大学医院
    B处的分子和医学病毒学,微生物学和卫生研究所,波鸿鲁尔大学,波鸿,德国
    Ç武汉病毒研究所,中国科学院,武汉市,中国人民共和国
    ð保罗·埃利希研究所,医学生物技术部,烂根,德国

摘要

诱导乙型肝炎病毒(HBV)的具体治疗免疫细胞毒性T细胞可能是一个战略治疗慢性乙型肝炎HBV的动物模型,旱獭,应用DNA疫苗表达土拨鼠肝炎病毒(WHV)核心抗原(WHcAg )导致长期控制病毒复制的抗病毒药物相结合。然而,很明显,使用更有效的疫苗需要克服WHV持久。因此,我们问是否使用修改后的疫苗和优化总理升压接种方案,可以实现更强大和功能更强大的T细胞反应。我们开发了一个新的DNA质粒(pCGWHc)的重组腺病毒(ADVS)WHcAg的高表达水平。免疫小鼠改进质粒pCGWHc的引起更强WHcAg特定的CD8 + T细胞,比以前使用的疫苗反应的。使用多色流式细胞仪和体内毒性实验,我们发现,在DNA总理ADV升压方案的免疫接种,在一个更​​加积极和功能的新质粒单独免疫反应的T细胞比。天真旱獭免疫与pCGWHc质粒或诱导1显著WHcAg具体脱粒应对挑战前ADVS,这种反应没有以前检测。一致,这种反应导致的迅速控制感染后的挑战。我们的研究结果表明,高抗原表达水平的DNA总理ADV提高免疫,改善在老鼠和旱獭引起显着的T细胞反应的T细胞反应。因此,这种新的疫苗接种策略,可能为治疗性疫苗对慢性乙肝病毒感染的候选人。
脚注

        2012年2月28日。
        2012年6月11日。
    通讯作者地址,michael.roggendorf单向due.de迈克尔Roggendorf。
作者: rocgao    时间: 2012-8-10 14:46

免疫疗法,明天的希望。楼主辛苦了。
作者: MP4    时间: 2012-8-11 07:29

题外话

[attach]328035[/attach]
http://www.uni-due.de/de/presse/meldung.php?id=1788
Prof. Yu-Mei Wen闻玉梅 mit Prof. Dr. med. Michael Roggendorf (l.), Prorektor Prof. Dr. rer. nat. Michael Farle und Prodekan Prof. Dr. med. Jan Buer (r.). Foto: Medienzentrum Klinikum

作者: 咬牙硬挺    时间: 2012-8-14 06:39

感谢分享!楼主好人
作者: 咬牙硬挺    时间: 2012-8-14 06:39

感谢分享!楼主好人




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