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Development of a time-resolved immunofluorometric assay for quantitation of mucosal and systemic antibody responses.

机译:时间分辨免疫荧光测定法的发展,用于定量粘膜和全身抗体反应。

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We developed a solid phase immunoassay that measured mucosal and systemic antibody responses from mice inoculated with either a staphylococcal enterotoxin B vaccine (SEBv) or noninfectious virus-like particles (VLP) of lentiviral origin. The assay used time-resolved fluorescence (TRF) with affinity-purified goat anti-mouse IgA and IgG conjugated to samarium and europium chelates, respectively. By employing these fluorogenic conjugates with different spectral emissions, IgA and IgG specific for SEB or VLP were readily detected in serum and saliva from mice inoculated intranasally. The TRF assay detected antigen-specific IgA in saliva 10 min after the addition of enhancement solution, while a conventional alkaline phosphatase-based assay for salivary IgA required 18 h after substrate addition. The TRF assay also provided a significantly higher signal-to-noise ratio and exhibited greater sensitivity. TRF assays detected both IgA and IgG in the same well, thereby reducing sample and reagent requirements.
机译:我们开发了一种固相免疫测定法,可以测量接种了葡萄球菌肠毒素B疫苗(SEBv)或慢病毒来源的非感染性病毒样颗粒(VLP)的小鼠的粘膜和全身抗体反应。该测定法使用了时间分辨荧光(TRF),以及亲和纯化的山羊抗小鼠IgA和IgG分别与sa和and螯合物结合。通过使用这些具有不同光谱发射的荧光结合物,可以很容易地在鼻内接种的小鼠的血清和唾液中检测到SEB或VLP特异性的IgA和IgG。加入增强溶液后10分钟,TRF分析检测到唾液中的抗原特异性IgA,而传统的基于碱性磷酸酶的唾液IgA分析则需要在添加底物后18小时。 TRF分析还提供了显着更高的信噪比并显示出更高的灵敏度。 TRF分析可在同一孔中同时检测IgA和IgG,从而减少了样品和试剂的需求。

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