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一种用于梅毒快速血清学诊断的新型重组抗原乳胶凝集试验(梅毒快速检测法)。

A new recombinant antigen latex agglutination test (Syphilis Fast) for the rapid serological diagnosis of syphilis.

作者信息

Young H, Moyes A, de Ste Croix I, McMillan A

机构信息

Department of Medical Microbiology, Edinburgh University Medical School, UK.

出版信息

Int J STD AIDS. 1998 Apr;9(4):196-200. doi: 10.1258/0956462981922034.

Abstract

We report an assessment of Syphilis Fast, a new latex test that uses a pool of 3 recombinant Treponema pallidum antigens (TpN15, TpN17, and TpN47) for the serodiagnosis of syphilis. Specificity was evaluated by screening 1518 unselected blood specimens in parallel with Syphilis Fast, the Captia SelectSyph-G EIA and the Venereal Disease Research Laboratory (VDRL) cardiolipin antigen test while sensitivity was tested using a panel of 99 treponemal sera (treated and untreated) representing various stages of infection and 15 treponemal sera detected on screening. The specificity of Syphilis Fast on initial testing (99.8%) was significantly higher (P<0.02) than that of Captia SelectSyph-G (99.2%) and the VDRL (99.1%): the specificity of Syphilis Fast remained significantly higher (P<0.02) after repeat testing (respective values 99.9%, 99.5% and 99.4%). There was no difference in the sensitivity of Syphilis Fast and Captia SelectSyph-G on initial (93% vs 92.1%) or repeat (95.6% vs 94.7%) testing: both were significantly more sensitive (P<0.001) than the VDRL (46.5% on initial and 43.9% on repeat testing). The sensitivities of the Treponema pallidum haemagglutination test (TPHA) and FTA-abs were 98.2% and 95.6% respectively. Negative reactions in Syphilis Fast and SelectSyph-G were associated with treated infections and correlated with low TPHA titres (< or = 80). We conclude that Syphilis Fast is a highly specific, simple and fast screening test with a sensitivity comparable to native antigen treponemal tests and that it merits consideration as a front-line screening test.

摘要

我们报告了对梅毒快速检测法(Syphilis Fast)的评估,这是一种新的乳胶检测法,它使用一组3种重组梅毒螺旋体抗原(TpN15、TpN17和TpN47)进行梅毒的血清学诊断。通过与梅毒快速检测法、Captia SelectSyph - G酶免疫测定法(EIA)和性病研究实验室(VDRL)心磷脂抗原检测法同时对1518份未经挑选的血液标本进行筛查来评估特异性,而使用一组99份代表感染不同阶段的梅毒血清(经治疗和未经治疗)以及在筛查中检测出的15份梅毒血清来测试敏感性。梅毒快速检测法初次检测时的特异性(99.8%)显著高于Captia SelectSyph - G(99.2%)和VDRL(99.1%)(P<0.02):重复检测后梅毒快速检测法的特异性仍显著更高(P<0.02)(相应值分别为99.9%、99.5%和99.4%)。梅毒快速检测法和Captia SelectSyph - G初次检测(93%对92.1%)或重复检测(95.6%对94.7%)时的敏感性没有差异:两者均比VDRL显著更敏感(P<0.001)(初次检测时为46.5%,重复检测时为43.9%)。梅毒螺旋体血凝试验(TPHA)和荧光螺旋体抗体吸收试验(FTA - abs)的敏感性分别为98.2%和95.6%。梅毒快速检测法和SelectSyph - G中的阴性反应与经治疗的感染相关,并且与低TPHA滴度(≤80)相关。我们得出结论,梅毒快速检测法是一种高度特异、简单且快速的筛查试验,其敏感性与天然抗原梅毒螺旋体检测法相当,值得作为一线筛查试验加以考虑。

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