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首页> 外文期刊>Parasites Vectors >Diagnostic efficacy of monoclonal antibody based sandwich enzyme linked immunosorbent assay (ELISA) for detection of Fasciola gigantica excretory/secretory antigens in both serum and stool
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Diagnostic efficacy of monoclonal antibody based sandwich enzyme linked immunosorbent assay (ELISA) for detection of Fasciola gigantica excretory/secretory antigens in both serum and stool

机译:基于单克隆抗体的夹心酶联免疫吸附法(ELISA)对巨大Fasciola gigantica血清和粪便中排泄/分泌抗原的检测的诊断功效

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Background This research was carried out to develop a reliable monoclonal antibody (MoAb)-based sandwich enzyme linked immunosorbent assay (ELISA) for the diagnosis of active Fasciola gigantica infection in both serum and stool for comparative purposes. Methods From a panel of MoAbs raised against F. gigantica excretory/secretory antigens (ES Ags), a pair (12B/11D/3F and 10A/9D/10G) was chosen due to its high reactivity and strict specificity to F. gigantica antigen by indirect ELISA. Results The two MoAbs were of the IgG1 and IgG2a subclasses, respectively. Using SDS-PAGE and EITB, the selected MoAbs recognized 83, 64, 45 and 26 kDa bands of ES Ags. The lower detection limit of ELISA assay was 3 ng/ml. In stool, the sensitivity, specificity and diagnostic efficacy of ELISA was 96%, 98.2 and 97.1%; while in serum they were 94%, 94.6% and 94.3%, respectively. Moreover, a positive correlation was found between ova count in stool of F. gigantica infected patients and the OD readings of ELISA in both stool and serum samples (r = 0.730, p < 0.01 and r = 0.608; p < 0.01, respectively). Conclusions These data showed that the use of MoAb-based sandwich ELISA for the detection of F. gigantica coproantigens in stool specimens was superior to serum samples; it provides a highly efficient, non-invasive technique for the diagnosis of active F. gigantica infection.
机译:背景进行这项研究以开发一种可靠的基于单克隆抗体(MoAb)的夹心酶联免疫吸附测定(ELISA),用于诊断血清和粪便中的巨大费氏Fasciola gigantica感染,以进行比较。方法从针对巨巨镰刀菌排泄/分泌抗原(ES Ags)的MoAb中选择一对(12B / 11D / 3F和10A / 9D / 10G),因为它们具有很高的反应性并且对巨巨镰刀菌抗原具有严格的特异性通过间接ELISA。结果两种MoAb分别为IgG1和IgG2a亚类。使用SDS-PAGE和EITB,选定的MoAb识别出ES Ag的83、64、45和26 kDa条带。 ELISA测定的下限为3 ng / ml。在粪便中,ELISA的敏感性,特异性和诊断效力分别为96%,98.2和97.1%;血清中分别为94%,94.6%和94.3%。此外,在感染巨巨F的患者的粪便中卵数与粪便和血清样品中ELISA的OD值呈正相关(分别为r = 0.730,p <0.01和r = 0.608; p <0.01)。结论这些数据表明,基于MoAb的夹心ELISA在粪便标本中检测巨型巨无花果原抗原的效果优于血清标本。它提供了一种有效的,无创的技术来诊断活跃的巨大巨球藻感染。

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