Durkin M M, Connolly P A, Wheat L J
Department of Medicine, Indiana University School of Medicine, Indianapolis 46262, USA.
J Clin Microbiol. 1997 Sep;35(9):2252-5. doi: 10.1128/jcm.35.9.2252-2255.1997.
The purpose of this study was to compare the conventional radioimmunoassay (RIA) to an enzyme-linked immunoassay (EIA) for the measurement of Histoplasma antigen in banked urine specimens. A correlation between the two methods would allow the EIA to be used as a nonradioactive alternative to the established 125I RIA. The study used stored urine from patients diagnosed with histoplasmosis during an outbreak in Indianapolis which began in 1988. Control specimens from healthy adults, patients with other fungal infections, urinary tract infections, or nonfungal pneumonia were also tested. Both the RIA and EIA were run concurrently. The RIA system measured antigen levels of 0.4 to 27.0 RIA units, while the EIA measured antigen levels of 0.6 to 20.1 units. Both the EIA and RIA detected measurable antigen levels in urine from 50 of 56 patients (89%) with disseminated disease and 11 of 30 patients (37%) with self-limiting disease. One of 96 control specimens, from a patient with paracoccidioidomycosis, was positive with both systems. Antigen levels measured by EIA correlated well with those measured by the established RIA method (correlation coefficient, 0.974). The EIA is an acceptable alternative to the RIA for measuring Histoplasma antigen levels in urine specimens.
本研究的目的是比较传统放射免疫测定法(RIA)和酶联免疫测定法(EIA)在检测储存尿液标本中组织胞浆菌抗原方面的差异。两种方法之间的相关性将使EIA能够作为已确立的125I RIA的非放射性替代方法。该研究使用了1988年印第安纳波利斯一次疫情期间被诊断为组织胞浆菌病患者的储存尿液。还对来自健康成年人、患有其他真菌感染、尿路感染或非真菌性肺炎患者的对照标本进行了检测。RIA和EIA同时进行。RIA系统检测到的抗原水平为0.4至27.0 RIA单位,而EIA检测到的抗原水平为0.6至20.1单位。EIA和RIA在56例播散性疾病患者中的50例(89%)以及30例自限性疾病患者中的11例(37%)的尿液中检测到了可测量的抗原水平。96份对照标本中的1份,来自一名副球孢子菌病患者,两种检测系统均呈阳性。EIA测定的抗原水平与已确立的RIA方法测定的抗原水平相关性良好(相关系数为0.974)。EIA是检测尿液标本中组织胞浆菌抗原水平时RIA的可接受替代方法。