首页> 美国卫生研究院文献>Journal of Visualized Experiments : JoVE >Developing a Salivary Antibody Multiplex Immunoassay to Measure Human Exposure to Environmental Pathogens
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Developing a Salivary Antibody Multiplex Immunoassay to Measure Human Exposure to Environmental Pathogens

机译:开发唾液抗体多重免疫测定法以测量人类暴露于环境病原体

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摘要

The etiology and impacts of human exposure to environmental pathogens are of major concern worldwide and, thus, the ability to assess exposure and infections using cost effective, high-throughput approaches would be indispensable. This manuscript describes the development and analysis of a bead-based multiplex immunoassay capable of measuring the presence of antibodies in human saliva to multiple pathogens simultaneously. Saliva is particularly attractive in this application because it is noninvasive, cheaper and easier to collect than serum. Antigens from environmental pathogens were coupled to carboxylated microspheres (beads) and used to measure antibodies in very small volumes of human saliva samples using a bead-based, solution-phase assay. Beads were coupled with antigens from Campylobacter jejuni, Helicobacter pylori, Toxoplasma gondii, noroviruses (G I.1 and G II.4) and hepatitis A virus. To ensure that the antigens were sufficiently coupled to the beads, coupling was confirmed using species-specific, animal-derived primary capture antibodies, followed by incubation with biotinylated anti-species secondary detection antibodies and streptavidin-R-phycoerythrin reporter (SAPE). As a control to measure non-specific binding, one bead set was treated identically to the others except it was not coupled to any antigen. The antigen-coupled and control beads were then incubated with prospectively-collected human saliva samples, measured on a high throughput analyzer based on the principles of flow cytometry, and the presence of antibodies to each antigen was measured in Median Fluorescence Intensity units (MFI). This multiplex immunoassay has a number of advantages, including more data with less sample; reduced costs and labor; and the ability to customize the assay to many targets of interest. Results indicate that the salivary multiplex immunoassay may be capable of identifying previous exposures and infections, which can be especially useful in surveillance studies involving large human populations.
机译:人类暴露于环境病原体的病因和影响是世界范围内的主要关注问题,因此,使用具有成本效益的高通量方法评估暴露和感染的能力将是必不可少的。该手稿描述了基于微珠的多重免疫测定法的开发和分析,该测定法能够同时测定人唾液中针对多种病原体的抗体的存在。唾液在该应用中特别有吸引力,因为它比血清无创,便宜且易于收集。来自环境病原体的抗原与羧化微球(珠子)偶联,并使用基于珠子的溶液相测定法,用于测量极少量人类唾液样品中的抗体。珠子与空肠弯曲杆菌,幽门螺杆菌,弓形虫,诺如病毒(G.1和G II.4)和甲型肝炎病毒的抗原结合。为了确保抗原与珠子充分偶联,使用物种特异性动物衍生的一级捕获抗体确认偶联,然后与生物素化的抗物种二级检测抗体和链霉亲和素-R-藻红蛋白报道分子(SAPE)一起孵育。作为测量非特异性结合的对照,一个珠子组与其他珠子组相同,但未与任何抗原偶联。然后将抗原偶联的珠子和对照珠子与前瞻性收集的人类唾液样品一起孵育,并根据流式细胞仪原理在高通量分析仪上进行测量,并以中值荧光强度单位(MFI)来测量针对每种抗原的抗体的存在。这种多重免疫测定具有许多优势,包括更多的数据和更少的样品;减少成本和劳动力;以及针对许多目标靶标定制化验的能力。结果表明,唾液多重免疫测定法可能能够识别以前的暴露和感染,这在涉及大量人群的监测研究中尤其有用。

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