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首页> 外文期刊>Clinical and diagnostic laboratory immunology >Neutralization Assay Using a Modified Vaccinia Virus Ankara Vector Expressing the Green Fluorescent Protein Is a High-Throughput Method To Monitor the Humoral Immune Response against Vaccinia Virus
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Neutralization Assay Using a Modified Vaccinia Virus Ankara Vector Expressing the Green Fluorescent Protein Is a High-Throughput Method To Monitor the Humoral Immune Response against Vaccinia Virus

机译:使用修饰的表达绿色荧光蛋白的痘苗病毒安卡拉载体进行中和测定是一种高通量方法,可监测针对痘苗病毒的体液免疫反应

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Vaccination against smallpox is again considered in order to face a possible bioterrorist threat, but the nature and the level of the immune response needed to protect a person from smallpox after vaccination are not totally understood. Therefore, simple, rapid, and accurate assays to evaluate the immune response to vaccinia virus need to be developed. Neutralization assays are usually considered good predictors of vaccine efficacy and more informative with regard to protection than binding assays. Currently, the presence of neutralizing antibodies to vaccinia virus is measured using a plaque reduction neutralization test, but this method is time-consuming and labor-intensive and has a subjective readout. Here, we describe an innovative neutralization assay based on a modified vaccinia virus Ankara (MVA) vector expressing the green fluorescent protein (MVA-gfp). This MVA-gfp neutralization assay is rapid and sensitive and has a high-throughput potential. Thus, it is suitable to monitor the immune response and eventually the efficacy of a large campaign of vaccination against smallpox and to study the vector-specific immune response in clinical trials that use genetically engineered vaccinia viruses. Most importantly, application of the highly attenuated MVA eliminates the safety concern in using the replication-competent vaccinia virus in the standard clinical laboratory.
机译:再次考虑针对天花的疫苗接种,以应对可能的生物恐怖威胁,但是,疫苗接种后保护人免于天花所需的免疫反应的性质和水平尚不完全清楚。因此,需要开发简单,快速和准确的测定方法来评估对牛痘病毒的免疫反应。中和测定通常被认为是疫苗效力的良好预测指标,并且在保护方面比结合测定更具参考价值。当前,使用斑块减少中和测试来测量针对牛痘病毒的中和抗体的存在,但是该方法耗时且费力并且具有主观的读数。在这里,我们描述了基于表达绿色荧光蛋白(MVA-gfp)的牛痘病毒安卡拉(MVA)载体的创新中和测定方法。这种MVA-gfp中和测定快速且灵敏,并且具有高通量潜力。因此,在使用基因工程牛痘病毒的临床试验中,它适合监测免疫反应以及最终针对天花的大规模疫苗接种运动的功效,并研究载体特异性免疫反应。最重要的是,高度减毒的MVA的应用消除了在标准临床实验室中使用具有复制能力的牛痘病毒的安全隐患。

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