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Abbott ARCHITECT I2000 based CMIA in detecting serum syphilis antibodies |
ZHANG Jianguang, DU Zhenhua, ZHANG Guifen |
Department of Clinical Laboratory, Characteristic Medical Center of Chinese People’s Armed Police Force, Tianjin 300162, China |
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Abstract Objective To investigate the applicability of Abbott ARCHITECT I2000 based chemiluminescent particle immunoassay (CMIA) in detecting serum syphilis antibodies. Methods Two hundred and seventy-one cases of CMIA positive serum samples (S/CO≥1.0) in syphilis screening were collected before these samples were retested using treponema pallidum particle agglutination (TPPA). The ability of CMIA to detect TPPA-positive cases was evaluated via receiver operating characteristic curve (ROC) analysis. Furthermore, these CMIA positive samples were divided into four groups according to their S/CO values: group A (1.0≤S/CO<3.0, n=85), group B (3.0≤S/CO<5.0, n=26), group C (5.0≤S/CO<7.0, n=17) and group D (S/CO≥7.0, n=143). The differences in TPPA positive rates among the four groups were analyzed. Meanwhile, a cutoff-positive rate curve was drawn to identify the optimal retest cutoff using TPPA. Results Among the 271 CMIA positive samples, 196 cases were positive for TPPA. The positive coincidence rates of TPPA retest from group A to group D were 20.00%, 76.92%, 94.12% and 100.00%, respectively, so the difference was statistically significant (W = 14253, P<0.001). When the reexamination cutoff was 5.1, the positive rate of TPPA reexamination reached 100%. Conclusions CMIA is of great value in detecting syphilis serum antibodies. It is recommended that positive CMIA results can be reported directly when S/CO value is above 5.1, and that TPPA reexamination shoud be performed when S/CO values range from 1.0 to 5.1. This strategy might be able to reduce false positive reports.
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Received: 20 October 2021
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[1] |
Cerqueira L R P,Monteiro D L M,Taquette S R,et al.The magnitude of syphilis:from prevalence to vertical transmission [J].Rev Inst Med Trop Sao Paulo, 2017, 59(21):78-82.
|
[2] |
童明宏,吴晓辉,王振华,等.化学发光微粒免疫分析法检测抗 TP 抗体的性能评价和应用[J]. 检验医学,2020,35(2):137-141.
|
[3] |
张 微,郭 楠,李宝萍,等.化学发光微粒子免疫检测梅毒抗体假阳性分析[J]. 中国卫生检验杂志,2021,31(10):1180-1182.
|
[4] |
金 晶,潘 玥,边春红,等.梅毒螺旋体特异性抗体试验方法探讨及临床应用价值评估[J].标记免疫分析与临床,2021, 28(1):27-31.
|
[5] |
王克迪,苏建荣.化学发光微粒子免疫检测发筛查梅毒的结果分析[J].首都医科大学学报,2016,3(4):419-522.
|
[6] |
段辉丽,向跃奎.微粒子化学发光免疫分析法在梅毒血清学检测中的应用[J].医学临床研究,2015,32(9):1845-1846.
|
[7] |
郑淑华,黄瑞玉,卢春敏,等.化学发光法和 TPPA 试验检测妇幼人群梅毒螺旋体抗体假阳性对比分析[J].中国皮肤性病学杂志,2021,35(3): 349-352.
|
[8] |
张立娟.化学发光法检测梅毒特异性抗体的效果评价[J].中国皮肤性病学杂,2019,33(10):1215-1218.
|
[9] |
魏 玲,庄 琪,陈智睿,等.CMIA与TPPA检测梅毒血清抗体阳性符合率比较及假阳性结果分析[J]. 中国保健营养,2020,30(32):305-306.
|
[10] |
刘 平,李志艳,冯珍如,等.化学反光微粒子免疫分析在梅毒螺旋体筛查中的应用探讨[J].标记免疫分析与临床,2016,23(9):1077-1079.
|
[11] |
文 卫,彭雪峰. 三种梅毒血清学试验的临床诊断价值比较[J].实用预防医学,2017,24(8):1007-1008.
|
[12] |
张 薇,车玉传.雅培ARCHITECT i2000SR 在梅毒实验室诊断中的临床应用和评价[J].检验医学与临床,2018,15(24):3721-3725.
|
[13] |
潘 杰,李蔼文,叶 青.探讨化学发光分析法的测量值在梅毒诊断中的应用[J]. 国际医药卫生导报2015,21(18):2761-2770.
|
[14] |
殷丽丽,姜繁明,于小鸥.化学发光法和TPPA试验检测梅毒抗体的比较及阳性符合率分析[J].中国中西医结合皮肤性病学杂志,2019,18(2):116-119.
|
|
|
|