Performance of Treponemal Tests for the Diagnosis of Syphilis

被引:84
作者
Park, Ina U. [1 ,2 ]
Fakile, Yetunde F. [2 ]
Chow, Joan M. [1 ]
Gustafson, Kathleen J. [1 ]
Jost, Heather [2 ]
Schapiro, Jeffrey M. [3 ]
Novak-Weekley, Susan [4 ]
Tran, Anthony [5 ]
Nomura, Jim H. [6 ]
Chen, Victor [6 ]
Beheshti, Manie [6 ]
Tsai, Townson [6 ]
Hoover, Karen [2 ]
Bolan, Gail [2 ]
机构
[1] Calif Dept Publ Hlth, Div Communicable Dis Control, Sexually Transmitted Dis Control Branch, Richmond, CA USA
[2] Ctr Dis Control & Prevent, Div Sexually Transmitted Dis Prevent, Atlanta, GA USA
[3] Kaiser Permanente Northern Calif, Reg Lab, Berkeley, CA USA
[4] Southern Calif Permanente Med Grp, Reg Reference Lab, North Hollywood, CA USA
[5] San Francisco Dept Publ Hlth, San Francisco, CA USA
[6] Southern Calif Permanente Med Grp, North Hollywood, CA USA
关键词
syphilis; immunoassay; treponemal; diagnostic performance; ENZYME-IMMUNOASSAY; SEROLOGICAL DIAGNOSIS; IMMUNOGLOBULIN-G; PALLIDUM;
D O I
10.1093/cid/ciy558
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background Treponemal immunoassays are increasingly used for syphilis screening with the reverse sequence algorithm. There are few data describing performance of treponemal immunoassays compared to traditional treponemal tests in patients with and without syphilis. Methods We calculated sensitivity and specificity of 7 treponemal assays: (1) ADVIA Centaur (chemiluminescence immunoassay [CIA]); (2) Bioplex 2200 (microbead immunoassay); (3) fluorescent treponemal antibody absorption test (FTA-ABS); (4) INNO-LIA (line immunoassay); (5) LIAISON CIA; (6) Treponema pallidum particle agglutination assay (TPPA); and (7) Trep-Sure (enzyme immunoassay [EIA]), using a reference standard combining clinical diagnosis and serology results. Sera were collected between May 2012-January 2013. Cases were characterized as: (1) current clinical diagnosis of syphilis: primary, secondary, early latent, late latent; (2) prior treated syphilis only; (3) no evidence of current syphilis, no prior history of syphilis, and at least 4 of 7 treponemal tests negative. Results Among 959 participants, 262 had current syphilis, 294 had prior syphilis, and 403 did not have syphilis. FTA-ABS was less sensitive for primary syphilis (78.2%) than the immunoassays or TPPA (94.5%-96.4%) (all P .01). All immunoassays were 100% sensitive for secondary syphilis, 95.2%-100% sensitive for early latent disease, and 86.8%-98.5% sensitive in late latent disease. TPPA had 100% specificity. Conclusions Treponemal immunoassays demonstrated excellent sensitivity for secondary, early latent, and seropositive primary syphilis. Sensitivity of FTA-ABS in primary syphilis was poor. Given its high specificity and superior sensitivity, TPPA is preferred to adjudicate discordant results with the reverse sequence algorithm over the FTA-ABS. We compared performance of 5 treponemal immunoassays, the Treponema pallidum particle agglutination assay (TPPA), and the fluorescent treponemal antibody absorption test (FTA-ABS). FTA-ABS was less sensitive for primary syphilis (78%) than the immunoassays or TPPA (94%-96% sensitivity). TPPA was 100% specific.
引用
收藏
页码:913 / 918
页数:6
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