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首页> 外文期刊>Clinical and vaccine immunology: CVI >Monoclonal antibodies specific for immunorecessive epitopes of glucuronoxylomannan, the major capsular polysaccharide of Cryptococcus neoformans, reduce serotype bias in an immunoassay for cryptococcal antigen
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Monoclonal antibodies specific for immunorecessive epitopes of glucuronoxylomannan, the major capsular polysaccharide of Cryptococcus neoformans, reduce serotype bias in an immunoassay for cryptococcal antigen

机译:单克隆抗体为immunorecessive具体glucuronoxylomannan抗原表位,专业隐球菌荚膜多糖的一个neoformans,降低血清型的偏见对隐球菌抗原免疫测定

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摘要

Immunoassay for detection of glucuronoxylomannan (GXM), the major capsular polysaccharide of Cryptococcus neoformans, is an important tool for diagnosis of cryptococcosis. However, immunoassays that are based solely or in part on detection with polyclonal antibodies may show serotype bias in detection of GXM, particularly limited sensitivity for serotype C. In this study, we describe detection of GXM in an antigen capture sandwich enzyme-linked immunosorbent assay (ELISA) that used a cocktail of two monoclonal antibodies (MAbs). MAb F12D2 was previously produced by immunization with GXM that had been treated to remove O-acetyl groups, a major source of serotype specificity. MAb F12D2 has a high degree of reactivity with GXM of serotypes A, B, C, and D, but the reactivity with serotype D was less than was found with other MAbs. MAb 339 is highly reactive with GXM of serotypes A and D. Use of a combination of the two MAbs produced an immunoassay that had the best properties of both MAbs, including good reactivity with serotype C, which is an emerging threat in sub-Saharan Africa. These results suggest that next-generation immunoassays for diagnosis of cryptococcosis may be formulated by (i) use of immunization and hybridoma screening strategies that are designed to prospectively meet the needs of immunoassay performance and (ii) careful selection of MAbs that span the expected polysaccharide serotypes in the subject patient population.
机译:免疫测定glucuronoxylomannan的检测(GXM),主要的荚膜多糖新型隐球菌,是一个重要的工具隐球菌病的诊断。完全或部分基于免疫测定多克隆抗体检测与显示在检测GXM血清型的偏见,特别是有限的血清型c。在这个敏感研究中,我们描述GXM的检测抗原捕捉夹心酶联免疫吸附试验(ELISA),使用两个的鸡尾酒单克隆抗体(mab)。以前产生的免疫与GXM被移除O-acetyl团体治疗,血清型特异性的主要来源。有高度的反应活性与GXM血清型A, B, C, D,但反应血清型D小于被发现与其他马伯。血清型和d使用的组合两个马伯产生免疫测定的最好的马伯的属性,包括好是一个新兴的反应性与血清型C在撒哈拉以南非洲地区的威胁。表明下一代免疫测定隐球菌病的诊断可能制定的(我)使用的免疫和杂种细胞筛选设计前瞻性的策略满足免疫测定的需求和性能(2)谨慎选择马伯的跨度预计多糖血清型的主题病人的人口。

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