Leland D S, Kohler R B
Department of Pathology, Indiana University Medical Center, Indianapolis 46202.
J Clin Microbiol. 1991 Oct;29(10):2220-3. doi: 10.1128/jcm.29.10.2220-2223.1991.
The purpose of this study was to evaluate the L-CLONE Legionella pneumophila Serogroup 1 Urine Antigen Latex Test (Access Medical Systems, Inc., Branford, Conn.) for detection of Legionella antigen in urine. A total of 481 frozen urine samples previously tested by an in-house solid-phase radioimmunoassay (RIA) was thawed and retested by using L-CLONE. Included in this sample were 140 RIA-positive samples from culture-positive or serologically confirmed cases of legionellosis and 341 RIA-negative samples from patients with non-Legionella respiratory disease or bacteriuria. The original RIA test result was accepted as the true value. L-CLONE correctly identified 76 of 140 (54%) known positive samples. False-negative results could not be attributed to a low Legionella antigen concentration or to a Legionella antigen subgroup. L-CLONE correctly identified 252 of 341 (74%) known negative samples. False-positive results were experienced in all groups of negative samples, regardless of the patients' underlying diseases. A total of 141 fresh urine samples was tested; all were Legionella antigen negative by RIA. L-CLONE provided 86% specificity. The sensitivity of the L-CLONE in testing fresh urine samples could not be evaluated because of the lack of Legionella antigen RIA-positive samples.
本研究的目的是评估L-CLONE嗜肺军团菌血清1型尿液抗原乳胶试验(Access Medical Systems公司,康涅狄格州布兰福德)用于检测尿液中军团菌抗原的效果。总共481份先前通过内部固相放射免疫测定法(RIA)检测过的冷冻尿液样本被解冻,并使用L-CLONE进行重新检测。该样本包括140份来自培养阳性或血清学确诊的军团菌病病例的RIA阳性样本,以及341份来自非军团菌呼吸道疾病或菌尿症患者的RIA阴性样本。原始的RIA检测结果被视为真值。L-CLONE正确识别出140份已知阳性样本中的76份(54%)。假阴性结果不能归因于军团菌抗原浓度低或军团菌抗原亚组。L-CLONE正确识别出341份已知阴性样本中的252份(74%)。在所有阴性样本组中均出现了假阳性结果,无论患者的基础疾病如何。总共检测了141份新鲜尿液样本;所有样本通过RIA检测均为军团菌抗原阴性。L-CLONE的特异性为86%。由于缺乏军团菌抗原RIA阳性样本,无法评估L-CLONE检测新鲜尿液样本的敏感性。