EVALUATION OF SYVA ENZYME-IMMUNOASSAY FOR THE DETECTION OF CHLAMYDIA-TRACHOMATIS IN UROGENITAL SPECIMENS

被引:15
作者
MONCADA, J
SCHACHTER, J
BOLAN, G
NATHAN, J
SHAFER, MA
CLARK, A
SCHWEBKE, J
STAMM, W
MROCZKOWSKI, T
SELIBORSKA, Z
MARTIN, DH
机构
[1] SAN FRANCISCO CITY CLIN,SAN FRANCISCO,CA
[2] UNIV CALIF SAN FRANCISCO,DEPT LAB MED,SAN FRANCISCO,CA 94143
[3] UNIV CALIF SAN FRANCISCO,DEPT PEDIAT,SAN FRANCISCO,CA 94143
[4] UNIV WASHINGTON,DEPT MED,SEATTLE,WA 98195
[5] LOUISIANA STATE UNIV,MED CTR,DEPT MED,NEW ORLEANS,LA 70112
关键词
D O I
10.1016/0732-8893(92)90068-5
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
A newly developed microwell enzyme immunosorbent assay (EIA) system by Syva Company (Palo Alto, CA) can detect Chlamydia trachomatis in <3 hr. It uses a polyclonal antibody to chlamydial lipopolysaccharide and end points are determined with a spectrophotometer. Three clinical trial sites (University of California Medical Center, San Francisco, CA; University of Washington, Seattle, WA; and Louisiana State University Medical Center, New Orleans, LA), compared this EIA with tissue culture (TC) for identifying Chlamydia in urogenital specimens. Overall prevalence by TC was 10.4% (136 of 1306). When tests were compared with TC (using vials or microtiter plates and a fluorescent antibody stain), we found an EIA sensitivity of 93.4% (127 of 136) and a specificity of 98.1% (1148 of 1170). This EIA has a performance profile that is, at the very least, comparable with other nonculture methods for diagnosing genital tract infections with C. trachomatis.
引用
收藏
页码:663 / 668
页数:6
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