Comparison of Six Automated Treponema-Specific Antibody Assays

Author:

Park Borae G.1ORCID,Yoon Jihoon G.1,Rim John Hoon1,Lee Anna2,Kim Hyon-Suk1

Affiliation:

1. Department of Laboratory Medicine, Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea

2. Seoul Clinical Laboratory, Seoul Medical Science Institute, Yongin, South Korea

Abstract

ABSTRACT Six different Treponema (TP)-specific immunoassays were compared to the fluorescent treponemal antibody absorption (FTA-ABS) test. A total of 615 samples were tested. The overall percent agreement, analytical sensitivity, and analytical specificity of each assay compared to the FTA-ABS test were as follows: Architect Syphilis TP, 99.2%, 96.8%, and 100%; Cobas Syphilis, 99.8%, 99.4%, and 100%; ADVIA Centaur Syphilis, 99.8%, 99.4%, and 100%; HISCL Anti-TP assay kit, 99.7%, 98.7%, and 100%; Immunoticles Auto3 TP, 99.0%, 97.5%, and 99.6%; Mediace TPLA, 98.0%, 98.1%, and 98.0%. All results that were discrepant between the TP-specific assays were associated with samples from noninfectious cases (11 immunoassay false positives and 7 from previous syphilis cases). Our study demonstrated that TP-specific immunoassays generally showed high sensitivities, specificities, and percentages of agreement compared to FTA-ABS, with rare cases of false-positive or false-negative results. Therefore, most TP-specific immunoassays are acceptable for use in screening for syphilis. However, it is important to perform a thorough review of a patient's clinical and treatment history for interpreting the results of syphilis serology.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

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