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首页> 外文期刊>Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis >Validation of a commercially available kit to detect anti- phosphatidylserine/prothrombin antibodies in a cohort of systemic lupus erythematosus patients
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Validation of a commercially available kit to detect anti- phosphatidylserine/prothrombin antibodies in a cohort of systemic lupus erythematosus patients

机译:验证市售试剂盒可检测系统性红斑狼疮患者群体中的抗磷脂酰丝氨酸/凝血酶原抗体

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Background Antiprothrombin antibodies detection comprises two different ELISAs: prothrombin coated on irradiated plates (aPT) or phosphatidylserine/ prothrombin (aPS/PT) as the antigen. While several commercial kits are available for the detection of aPT, aPS/PT are usually detected by in-house assays. Recently, a new commercially available kit was launched and, therefore, we decided to test its efficiency by comparing it to our in-house assay. Methods aPS/PT were tested by our in-house assay (aPS/PTih) in 75 SLE patients, using Immulon 1 plates coated with phosphatidylserine, purified human prothrombin and 1%BSA-TBS-CaCl as blocking and diluents. Data from this assay were compared to those obtained by the QUANTA Lite? aPS/PT screen, IgG and IgM Elisa (INOVA Diagnostics, Inc, San Diego, USA) commercial kits (aPS/PT c). Results aPS/PT were found in 41.3% and 46.7% of SLE patients by the aPS/PTih and the aPS/PTc, respectively. There was a positive correlation between IgG aPS/PTih and aPS/PTc assays (R2 = 0. 861 by Spearman test, p = 0.0027). Sensitivity and specificity for APS were 62.2% and 97.4% (AUC 0.780) for the aPS/PTih assay and 70.3% and 84.2% (AUC 0.858) for the aPS/PTC. Shorter running times were also seen when comparing the aPS/PTih vs. aPS/PTc (7 hours vs. 3 hours, respectively). Conclusion The aPS/PTC is a reproducible and accurate test for the detection of aPS/PT, bringing also the advantage of shorter running times.
机译:背景技术抗凝血酶原抗体检测包括两种不同的ELISA:涂在辐射板上的凝血酶原(aPT)或磷脂酰丝氨酸/凝血酶原(aPS / PT)作为抗原。尽管有几种商用试剂盒可用于检测aPT,但通常通过内部分析来检测aPS / PT。最近,推出了一种新的市售试剂盒,因此,我们决定通过将其与我们的内部检测方法进行比较来测试其效率。方法采用我们的内部检测(aPS / PTih)在75位SLE患者中使用涂有磷脂酰丝氨酸,纯化的人类凝血酶原和1%BSA-TBS-CaCl的Immulon 1板作为封闭剂和稀释剂,对aPS / PT进行了测试。将来自该测定的数据与通过QUANTA Lite?获得的数据进行比较。 aPS / PT屏幕,IgG和IgM Elisa(INOVA Diagnostics,Inc,美国圣地亚哥)商业试剂盒(aPS / PT c)。结果通过aPS / PTih和aPS / PTc分别在SLE患者中发现aPS / PT占41.3%和46.7%。 IgG aPS / PTih与aPS / PTc分析之间存在正相关(通过Spearman检验,R2 = 0. 861,p = 0.0027)。对于aPS / PTih分析,APS的敏感性和特异性分别为62.2%和97.4%(AUC 0.780),对aPS / PTC的敏感性和特异性分别为70.3%和84.2%(AUC 0.858)。比较aPS / PTih与aPS / PTc时,运行时间也更短(分别为7小时和3小时)。结论aPS / PTC是检测aPS / PT的可重复且准确的测试,还具有运行时间更短的优势。

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