梅毒
医学
密螺旋体
免疫分析
免疫学
人口
密螺旋体病
抗体
性传播疾病
病毒学
环境卫生
人类免疫缺陷病毒(HIV)
作者
Ernest Wong,Jeffrey D. Klausner,Gloria Caguin-Grygiel,Carmela Madayag,Kim O. Barber,Julia S. Qiu,Sally Liska,Mark Pandori
标识
DOI:10.1097/olq.0b013e318205491a
摘要
In Brief Background: Increasing interest in the use of enzyme immunoassays (EIA) for syphilis screening has generated a considerable need for data on the performance of such tests. Methods: We compared the performance of 1 EIA, the TREP-SURE EIA to that of the Venereal Disease Research Laboratory (VDRL) and Treponema pallidum particle agglutination assay (TPPA) in the detection of infection with Treponema pallidum. In total, 674 specimens were tested by VDRL and EIA (356 VDRL-nonreactive and 318 VDRL-reactive). All specimens that were found to be reactive by either the VDRL or EIA were subsequently analyzed by TPPA. Results: We found that the TREP-SURE EIA was marginally less sensitive than the VDRL test for screening, but was significantly more specific. All EIA-TPPA discordant specimens were analyzed by multiple tests, including Immunoglobulin M- and G-specific Western blots and an IgM-specific EIA. Signal-to-cutoff ratios (index values) generated by the TREP-SURE EIA were also investigated. It was found that these values may be instructive regarding the interpretation of test results, as they were found to correlate strongly with the probability of positivity on a TPPA assay. Specimens that reacted positively on the EIA with very high index values were found overwhelmingly to be reactive by TPPA, perhaps obviating the need for the testing of most EIA positive specimens with a secondary treponemal test. Conclusions: An IgM/IgG sensitive EIA would be an effective alternative to VDRL for syphilis screening. Using the EIA index values may provide additional, helpful information to the diagnostic process. This study compares an enzyme immunoassay to a nontreponemal test (Venereal Disease Research Laboratory) for syphilis screening. The index values of enzyme immunoassay results were correlated with Treponema pallidum particle agglutination assay reactivity.
科研通智能强力驱动
Strongly Powered by AbleSci AI