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用于梅毒早期诊断和管理的特异性抗体评估。

Evaluation of specific antibodies for early diagnosis and management of syphilis.

作者信息

Dang Qianli, Feng Jie, Lu Xuedang, Zhang Xiaoyan, Xu Hanqing, Liu Chao, Nu Xinwu

机构信息

Dermatology of No. 2 Hospital, Xi'an Jiaotong University, Xi'an, Shaanxi, China.

出版信息

Int J Dermatol. 2006 Oct;45(10):1169-71. doi: 10.1111/j.1365-4632.2006.02869.x.

DOI:10.1111/j.1365-4632.2006.02869.x
PMID:17040431
Abstract

For many years, tests for cardiolipin antibodies Tp15, Tp17, Tp45, Tp47, and other specific Treponema pallidum antibodies, have been used to diagnose syphilis, but the timing and rates of antibody detection differ in primary and secondary syphilis. Our objective was to determine the value of the rapid plasma reagin (RPR) test, T. pallidum passive particle agglutination (TPPA) assay and Western blotting (WB) in the diagnosis of early syphilis, by studying 67 patients (20 with primary and 47 with secondary syphilis) over a recent 5-year period. All patients were tested before and 21/67 were tested after treatment. Western blotting showed that while there was a difference within the study group in terms of the number of bands detected, all patients with primary syphilis demonstrated the 47-kDa antibody, but RPR and TPPA were negative in some patients. Eighteen to 24 months after treatment, 21/67 patients were tested by WB and TPPA; antibodies to T. pallidum became undetectable within 24 months after treatment in 29% of patients. By RPR, 29% patients had negative titers within 6 months of treatment, and 86% returned to normal within 24 months. We conclude that detection of specific 47-kDa T. pallidum antibodies can be used to diagnose primary syphilis. By RPR, antibodies disappear in 6-24 months after treatment in many patients, suggesting that a change in titer may be an indicator of treatment success.

摘要

多年来,心磷脂抗体Tp15、Tp17、Tp45、Tp47以及其他梅毒螺旋体特异性抗体检测一直用于梅毒诊断,但一期和二期梅毒抗体检测的时机和阳性率有所不同。我们的目的是通过对67例患者(20例一期梅毒和47例二期梅毒)进行近5年的研究,确定快速血浆反应素(RPR)试验、梅毒螺旋体被动颗粒凝集试验(TPPA)和免疫印迹法(WB)在早期梅毒诊断中的价值。所有患者在治疗前均接受检测,67例中有21例在治疗后接受检测。免疫印迹法显示,虽然研究组内检测到的条带数量存在差异,但所有一期梅毒患者均显示出47 kDa抗体,但部分患者RPR和TPPA呈阴性。治疗后18至24个月,67例中有21例接受WB和TPPA检测;29%的患者在治疗后24个月内梅毒螺旋体抗体检测不到。通过RPR检测,29%的患者在治疗后6个月内滴度转阴,86%的患者在24个月内恢复正常。我们得出结论,检测特异性47 kDa梅毒螺旋体抗体可用于诊断一期梅毒。通过RPR检测,许多患者在治疗后6至24个月抗体消失,这表明滴度变化可能是治疗成功的一个指标。

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