Myerson D, Lingenfelter P A, Gleaves C A, Meyers J D, Bowden R A
Division of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, WA 98104.
Am J Clin Pathol. 1993 Oct;100(4):407-13. doi: 10.1093/ajcp/100.4.407.
The authors developed a polymerase chain reaction (PCR) procedure to detect cytomegalovirus (CMV) in archived, frozen lung tissue and bronchoalveolar lavage (BAL) fluid preparations. The procedure incorporated an internal beta-globin control to assess the adequacy of the sample. Twenty-nine lung tissue and 96 archived BAL specimens from marrow transplant recipients were tested. One of the lung tissue specimens and 46 of the BAL specimens had insufficient tissue for PCR analysis because they did not show a beta-globin band. In lung tissue, the PCR had a sensitivity of 100% and specificity of 89% compared with conventional tube culture. In BAL specimens, the PCR had a sensitivity of 87% and specificity of 90% compared with conventional tube culture or centrifugation culture. Provided tissue was sufficient, the results suggest that the PCR can be used to diagnose CMV interstitial pneumonia effectively from frozen specimens of lung tissue or BAL fluid.
作者研发了一种聚合酶链反应(PCR)程序,用于检测存档的冷冻肺组织和支气管肺泡灌洗(BAL)液制剂中的巨细胞病毒(CMV)。该程序纳入了一个内部β-珠蛋白对照,以评估样本的充足性。对来自骨髓移植受者的29份肺组织和96份存档BAL标本进行了检测。其中1份肺组织标本和46份BAL标本因未显示β-珠蛋白条带而没有足够的组织用于PCR分析。在肺组织中,与传统试管培养相比,PCR的灵敏度为100%,特异性为89%。在BAL标本中,与传统试管培养或离心培养相比,PCR的灵敏度为87%,特异性为90%。如果组织足够,结果表明PCR可用于从冷冻的肺组织或BAL液标本中有效诊断CMV间质性肺炎。