...
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
【24h】

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:特异性针对葡糖醛酸羟甘露聚糖(新隐球菌的主要荚膜多糖)的免疫原性抗原决定簇的单克隆抗体可降低针对隐球菌抗原的免疫分析的血清型偏倚。

获取原文
           

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:用于检测葡糖醛酸羟甘露聚糖(GXM)的免疫测定是新型隐球菌的主要荚膜多糖,是诊断隐球菌病的重要工具。但是,仅基于或部分基于多克隆抗体检测的免疫分析法可能会在GXM检测中显示血清型偏倚,特别是对C型血清型的敏感性有限。在这项研究中,我们描述了在抗原捕获三明治酶联免疫吸附测定中检测GXM (ELISA)使用两种单克隆抗体(MAb)的混合物。单克隆抗体F12D2以前是通过用GXM免疫产生的,该疫苗经过处理可去除 O -乙酰基,血清型特异性的主要来源。 MAb F12D2与血清型A,B,C和D的GXM具有高度的反应性,但与血清型D的反应性比其他MAb少。 MAb 339与血清型A和D的GXM具有高度反应性。两种MAb的组合使用产生的免疫测定具有两种MAb的最佳特性,包括与血清型C的良好反应性,这在撒哈拉以南非洲正在成为威胁。这些结果表明,可以通过以下方式制定用于诊断隐球菌病的下一代免疫测定法:(i)使用旨​​在满足免疫测定性能需求的免疫和杂交瘤筛选策略,以及(ii)仔细选择跨越预期多糖的单克隆抗体患者人群中的血清型。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号