首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Utility of the Focus Technologies West Nile Virus Immunoglobulin M Capture Enzyme-Linked Immunosorbent Assay for Testing Cerebrospinal Fluid
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Utility of the Focus Technologies West Nile Virus Immunoglobulin M Capture Enzyme-Linked Immunosorbent Assay for Testing Cerebrospinal Fluid

机译:Focus Technologies西尼罗河病毒免疫球蛋白M捕获酶联免疫吸附测定法在测试脑脊液中的实用性

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摘要

Focus Technologies has developed an immunoglobulin M (IgM) capture enzyme-linked immunosorbent assay (ELISA) kit that utilizes recombinant West Nile virus (WNV) antigens to detect WNV IgM in serum. We evaluate here the utility of the kit for detecting WNV IgM in cerebrospinal fluid (CSF). The sensitivity was evaluated by using 52 CSF specimens from the 2002 WNV season that were positive in both the Public Health Service Laboratories WNV IgM ELISA and an in-house WNV IgM ELISA with native WNV antigen. The specificity was evaluated with two groups of specimens: (i) 73 CSF specimens submitted for in-house WNV IgM ELISA testing from February through April 2003 and yielding a negative WNV IgM result and (ii) 60 CSF specimens determined to be positive for another virus by PCR testing. Using these 185 CSF specimens at a screening dilution of 1:2, the kit was determined to be 100% sensitive and 100% specific. Endpoint titers were determined for 20 IgM-positive CSF specimens by testing serial twofold dilutions and ranged from 1:8 to 1:512. Index values (specimen absorbance value/calibrator absorbance value) for the screening dilution (1:2) showed no correlation with IgM titers, whereas index values for higher dilutions showed significant correlation with IgM titers. CSF screening dilutions of greater than 1:2 are not recommended, however, due to the risk of obtaining false-negative results. These findings show that the Focus Technologies WNV IgM capture ELISA, when utilized as recommended, offers accurate qualitative detection of WNV IgM in CSF specimens.
机译:Focus Technologies开发了一种免疫球蛋白M(IgM)捕获酶联免疫吸附测定(ELISA)试剂盒,该试剂盒利用重组西尼罗河病毒(WNV)抗原检测血清中的WNV IgM。我们在这里评估该试剂盒在脑脊液(CSF)中检测WNV IgM的实用性。通过使用2002年WNV季节的52例CSF标本对敏感性进行评估,这些标本在公共卫生服务实验室WNV IgM ELISA和带有天然WNV抗原的内部WNV IgM ELISA中均呈阳性。用两组样本评估了特异性:(i)从2003年2月至2003年4月提交73份CSF样本进行内部WNV IgM ELISA检测,并产生阴性的WNV IgM结果;(ii)60份CSF样本被确定对另一份样本呈阳性PCR检测病毒。使用筛选稀释度为1:2的这185个CSF标本,确定该试剂盒具有100%的敏感性和100%的特异性。通过测试系列两倍稀释液,确定20 IgM阳性CSF标本的终点滴度,范围为1:8至1:512。筛选稀释液(1:2)的指标值(标本吸光度值/校正剂吸收率值)与IgM滴度无相关性,而更高稀释度的指标值与IgM滴度显着相关。不建议将CSF筛查稀释度大于1:2,因为存在获得假阴性结果的风险。这些发现表明,按推荐使用Focus Technologies WNV IgM捕获ELISA可以准确定量检测CSF标本中的WNV IgM。

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