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首页> 外文期刊>Veterinary Immunology and Immunopathology >Measuring CMI responses using the PrimeFlow RNA assay: A new method of evaluating BVDV vaccination response in cattle
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Measuring CMI responses using the PrimeFlow RNA assay: A new method of evaluating BVDV vaccination response in cattle

机译:使用Primeflow RNA测定测量CMI响应:一种评估牛的BVDV疫苗接种反应的新方法

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Current methods for evaluating bovine viral diarrhea virus (BVDV) vaccination response typically rely on measurement of humoral responses as determined by virus neutralizing antibody titers (VNT) against BVDV. While VNT are correlated with increased protection, research has also shown that cell mediated immunity (CMI) is an important component of a protective response against BVDV. For example, improved protection against BVDV by modified-live viral (MLV) vaccines as compared to killed vaccines is thought to be due to better CMI induced by the MLV. The goal of this work was to evaluate the cell mediated response in vaccinated calves using a novel PrimeFlow RNA assay that incorporates cell surface marker staining with intracellular RNA expression of cytokines and viral RNA detection. Results from this study evaluating mRNA for IFN-gamma and IL-2 at 24 h post-BVDV stimulation are similar to previous studies in which IFN-y was detected in the CD4(+) and CD8(+) T cell population. However, a novel observation was the detection of IFN-gamma mRNA in the NK cell population in vaccinated animals. The NK cell population contributed a significant portion of the IFN-gamma produced. This study also demonstrated a decrease in the frequency and amount of BVDV in PBMCs, harvested from vaccinated calves and exposed to BVDV in vitro. Collectively data from this study highlights the association between an increase in IFN-gamma and a decreased infection rate of isolated PBMC's, based on the frequency and amount of BVDV positive cells following in vitro exposure. This new method combines not only the ability to evaluate cellular responses, but also the ability to understand potential antiviral properties associated with cellular responses. This is the first assay to describe and simultaneously measure CMI responses and intracellular viral RNA quantity as a method to evaluate protective responses associated with vaccination.
机译:评估牛病毒腹泻病毒(BVDV)疫苗接种响应的目前方法通常依赖于通过对BVDV的病毒中和抗体滴度(VNT)测定的体液反应的测量。虽然VNT与增加的保护相关,但研究还表明,细胞介导的免疫(CMI)是对BVDV的保护响应的重要组成部分。例如,与杀死疫苗相比,通过改性活病毒(MLV)疫苗对BVDV的改善保护被认为是由于MLV诱导的更好的CMI。本作作品的目的是使用新的Primeflow RNA测定法评估疫苗接种牛犊的呼应,其包括细胞内部RNA表达细胞因子和病毒RNA检测的细胞表面标记染色。本研究的结果评估了24小时后IFN-Gamma和IL-2的MRNA,其BVDV刺激类似于先前的研究,其中在CD4(+)和CD8(+)T细胞群中检测到IFN-Y。然而,新的观察是在接种疫苗的动物中检测NK细胞群中的IFN-γmRNA。 NK细胞群有助于产生IFN-Gamma的重要部分。该研究还证明了PBMC中BVDV的频率和量的降低,从接种疫苗的犊牛收获并在体外暴露于BVDV。本研究的集体数据突出了IFN-Gamma的增加与分离PBMC的频率降低的关联,基于体外暴露后BVDV阳性细胞的频率和量。这种新方法不仅结合了评估细胞反应的能力,还结合了理解与细胞反应相关的潜在抗病毒性质的能力。这是第一种用于描述和同时测量CMI响应和细胞内病毒RNA量作为评估与疫苗接种相关的保护反应的方法的试验。

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