N S Rote, K G Nielsen, V D Neilson, H R Hill, J R Scott
{"title":"酶联免疫吸附法(ELISA)检测抗血小板抗体与新生儿短暂性血小板减少性紫癜的研究。","authors":"N S Rote, K G Nielsen, V D Neilson, H R Hill, J R Scott","doi":"10.1111/j.1600-0897.1983.tb00242.x","DOIUrl":null,"url":null,"abstract":"<p><p>Autoimmune thrombocytopenic purpura (ATP) is an antibody-mediated autoimmune disease of platelets. Transplacental passage of the antibody during pregnancy can result in transient neonatal thrombocytopenia, but it is not known why some infants of antibody-positive, thrombocytopenic mothers are not affected. We have developed a competitive enzyme-linked immunosorbent assay (ELISA) to measure circulating antiplatelet antibody and have used this technique to investigate the influence of maternal titers on the occurrence of neonatal thrombocytopenia. The assay is sensitive over a range of 12.5 to 800 ng of immunoglobulin G (IgG) per microtiter well and closely correlates with the complement lysis inhibition assay (CLIA) for antiplatelet antibody (correlation coefficient = 0.726). In many instances, the level of circulating antiplatelet antibody in maternal and cord bloods reflected the degree of maternal and neonatal thrombocytopenia, but several important exceptions were observed. We suggest that levels of antiplatelet antibody in the maternal blood and cord blood are not always predictive of the degree of neonatal thrombocytopenia.</p>","PeriodicalId":79203,"journal":{"name":"American journal of reproductive immunology : AJRI : official journal of the American Society for the Immunology of Reproduction and the International Coordination Committee for Immunology of Reproduction","volume":"3 4","pages":"178-82"},"PeriodicalIF":0.0000,"publicationDate":"1983-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/j.1600-0897.1983.tb00242.x","citationCount":"8","resultStr":"{\"title\":\"Studies by enzyme-linked immunosorbent assay (ELISA) of antiplatelet antibody and transient neonatal thrombocytopenic purpura.\",\"authors\":\"N S Rote, K G Nielsen, V D Neilson, H R Hill, J R Scott\",\"doi\":\"10.1111/j.1600-0897.1983.tb00242.x\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Autoimmune thrombocytopenic purpura (ATP) is an antibody-mediated autoimmune disease of platelets. Transplacental passage of the antibody during pregnancy can result in transient neonatal thrombocytopenia, but it is not known why some infants of antibody-positive, thrombocytopenic mothers are not affected. We have developed a competitive enzyme-linked immunosorbent assay (ELISA) to measure circulating antiplatelet antibody and have used this technique to investigate the influence of maternal titers on the occurrence of neonatal thrombocytopenia. The assay is sensitive over a range of 12.5 to 800 ng of immunoglobulin G (IgG) per microtiter well and closely correlates with the complement lysis inhibition assay (CLIA) for antiplatelet antibody (correlation coefficient = 0.726). In many instances, the level of circulating antiplatelet antibody in maternal and cord bloods reflected the degree of maternal and neonatal thrombocytopenia, but several important exceptions were observed. 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引用次数: 8
摘要
自身免疫性血小板减少性紫癜(ATP)是一种抗体介导的血小板自身免疫性疾病。妊娠期间经胎盘传递该抗体可导致新生儿短暂性血小板减少,但尚不清楚为什么抗体阳性、血小板减少的母亲的一些婴儿不受影响。我们开发了一种竞争性酶联免疫吸附试验(ELISA)来测量循环抗血小板抗体,并使用该技术来研究母体滴度对新生儿血小板减少症发生的影响。该方法对免疫球蛋白G (IgG)的灵敏度在12.5 ~ 800 ng /微滴孔之间,与补体溶解抑制试验(CLIA)的抗血小板抗体密切相关(相关系数= 0.726)。在许多情况下,母体和脐带血中循环抗血小板抗体的水平反映了母体和新生儿血小板减少症的程度,但也观察到一些重要的例外情况。我们认为母体血液和脐带血中的抗血小板抗体水平并不总是预测新生儿血小板减少症的程度。
Studies by enzyme-linked immunosorbent assay (ELISA) of antiplatelet antibody and transient neonatal thrombocytopenic purpura.
Autoimmune thrombocytopenic purpura (ATP) is an antibody-mediated autoimmune disease of platelets. Transplacental passage of the antibody during pregnancy can result in transient neonatal thrombocytopenia, but it is not known why some infants of antibody-positive, thrombocytopenic mothers are not affected. We have developed a competitive enzyme-linked immunosorbent assay (ELISA) to measure circulating antiplatelet antibody and have used this technique to investigate the influence of maternal titers on the occurrence of neonatal thrombocytopenia. The assay is sensitive over a range of 12.5 to 800 ng of immunoglobulin G (IgG) per microtiter well and closely correlates with the complement lysis inhibition assay (CLIA) for antiplatelet antibody (correlation coefficient = 0.726). In many instances, the level of circulating antiplatelet antibody in maternal and cord bloods reflected the degree of maternal and neonatal thrombocytopenia, but several important exceptions were observed. We suggest that levels of antiplatelet antibody in the maternal blood and cord blood are not always predictive of the degree of neonatal thrombocytopenia.