用梅毒螺旋体颗粒凝集(tppa)试验对献血者进行梅毒自动筛查的评价

S. Sato, S. Kishimoto, Kazuhiro Kuzuma, Ryouichi Maeda, T. Kato, H. Ikeda, S. Sekiguchi
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引用次数: 0

摘要

新近开发的梅毒感染检测方法梅毒螺旋体颗粒凝集(TPPA, Fujrebio)对6名新近感染梅毒患者的血清显示阳性反应。结果通过酶免疫测定(Imzyn M-TP, Fujirebio)和/或免疫荧光(FTA-ABS, Nihon Touketukansou)等其他免疫测定法证实。血清tp (Fujirebio)检测结果为阴性。在血清转化组中,TPPA比常规RPR(快速血浆反应,Kaketuken)更早出现阳性反应。5例新近感染患者的IgM检测结果均为TPPA阳性,而血清tp检测结果仅为1例阳性。这些结果表明,TPPA能够在感染的早期阶段检测到抗tp。下一步,我们用PK7200自动输血前凝集分析仪(奥林巴斯)评估了该试验在献血者筛选中的应用。建立PK7200中TPPA的最佳检测条件(PK-TPPA)后,对4902份样品同时进行人工和自动化检测。阳性样本被人工重新检测。PK测试没有假阴性结果,而两种人工PK测试产生假阳性结果的比率相似。同时检测PK-TPPA和RPR, 14106份供体样品中分别有43份和65份重复阳性。在两项检测均呈阳性的21份样本中,17份经FTA-ABS检测为IgG型抗tp抗体。20份PK-TPPA(+)RPR(-)样品中,7份IgG型抗tp阳性。44份RPR(+)- tppa(-)样品均无FTA-ABS阳性。我们的结论是,PK-TPPA对检测IgM型抗tp足够敏感,可用于供体筛选。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
EVALUATION OF AUTOMATED SYPHILIS SCREENING FOR BLOOD DONORS USING TREPONEMA PALLLIDUM PARTICLE AGGLUTINATION (TPPA) TEST
Sera obtained from six patients with recently infected syphilis showed positive reaction by Treponema pallidum Particle Agglutination (TPPA, Fujrebio), a newly developed test for syphilis infection. The results were confirmed by other immunoassays such as enzyme immunoassay (Imzyn M-TP, Fujirebio) and/or immunofluorescence (FTA-ABS, Nihon Touketukansou). In contrast, they were negative by Serodia-TP (Fujirebio). In a seroconversion panel, TPPA showed positive reaction earlier than conventional RPR (rapid plasma reagin, Kaketuken). IgM fractions prepared from five recently infected patients were all positive by TPPA, while only one was positive by Serodia-TP. These results indicate that TPPA is able to detect anti-TP in the early phase of infection. In the next step, we evaluated the application of this test for blood donor screening with a PK7200 automated pretransfusion analyzer for agglutination assays (Olympus). After establishing optinal conditions for TPPA in the PK7200 (PK-TPPA), 4,902 samples were simultaneously tested by manual and automated testing. Positive samples were manually retest ed. There was no false negative results by the PK test, while both the manual PK tests yielded a similar rate of false positive results. In a simultaneous test with PK-TPPA and RPR, respec tively 43 and 65 of 14,106 donor samples were repeatedly positive. Of 21 samples showing positive reaction in both tests, 17 were confirmed as IgG type anti-TP by FTA-ABS. Of 20 PK-TPPA(+)RPR(-) samples, 7 were IgG type anti-TP positive. None of the 44 RPR(+)-TPPA(-) samples were positive by FTA-ABS. We conclude that the PK-TPPA is sensitive enough to detect IgM type anti-TP and acceptable for donor screening.
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