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首页> 外文期刊>Journal of Clinical Microbiology >Multicenter evaluation of a fluorometric enzyme immunocapture assay to detect toxoplasma-specific immunoglobulin M in dried blood filter paper specimens from newborns.
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Multicenter evaluation of a fluorometric enzyme immunocapture assay to detect toxoplasma-specific immunoglobulin M in dried blood filter paper specimens from newborns.

机译:荧光酶联免疫吸附测定的多中心评估,以检测新生儿干血滤纸标本中的弓形虫特异性免疫球蛋白M。

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An easy-to-perform fluorometric enzyme immunocapture assay (FEIA) was developed by Labsystems, Helsinki, Finland, to detect toxoplasma-specific immunoglobulin M (IgM) in dried blood spots. Assay materials were distributed to two sites that have programs in place designed to identify infants born with congenital toxoplasma infection: the Statens Serum Institut, Copenhagen, Denmark, and the New England Regional Newborn Screening Program, Boston, Mass. Each site tested over 700 dried blood samples from healthy newborns to define a cutoff at the 99.5 percentile (5 enzyme immunounits for Copenhagen and 4 enzyme immunounits for Boston). Each site then applied its own cutoff of interpret results for dried blood spots prepared from either adults with serology suggestive of acute infection (Copenhagen) or infants determined to be congenitally infected on the basis of serological criteria (Boston). In Copenhagen, 35 of 38 adult samples were either positive to a small degree or borderline positive for IgA. These samples thus may not represent acute infection. In Boston, of 26 congenitally infected infants, 22 were positive by FEIA. The four infant specimens not positive by FEIA were either negative or borderline positive by the standard Boston assay. These results demonstrate that the IgM FEIA is a potential alternative to other filter paper assay for toxoplasma-specific IgM currently in use for newborns.
机译:芬兰赫尔辛基Labsystems开发了一种易于执行的荧光酶免疫捕获测定(FEIA),以检测干血斑中的弓形虫特异性免疫球蛋白M(IgM)。将测定材料分发到两个地点,这些地点设有旨在识别先天性弓形虫感染的婴儿的计划:丹麦哥本哈根的史坦顿血清研究所和马萨诸塞州波士顿的新英格兰地区新生儿筛查计划。每个地点都测试了700多个干燥的采集健康新生儿的血液样本,以在99.5个百分点处确定临界值(哥本哈根的5个酶免疫单位和波士顿的4个酶免疫单位)。然后,每个站点将其解释结果的截止值用于从具有急性感染血清学的成人(哥本哈根)或根据血清学标准确定为先天感染的婴儿(波士顿)制备的干血斑。在哥本哈根,38个成人样本中有35个样本的IgA阳性或略有阳性。因此,这些样本可能并不代表急性感染。在波士顿,有26名先天感染的婴儿中,有22名FEIA呈阳性。根据标准波士顿分析,FEIA未呈阳性的四个婴儿标本为阴性或临界阳性。这些结果表明,对于目前用于新生儿的弓形虫特异性IgM,IgM FEIA是其他滤纸测定的潜在替代品。

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