Evaluation Of Real-time Pcr Assay For Diagnosis Of Pcp U

实时 PCR 检测诊断 Pcp U 的评估

• 批准号: 6825576
• 负责人: Steven h FISCHER
• 金额: --
• 依托单位: CLINICAL CENTER
• 依托单位国家: 美国
• 资助国家: 美国
• 起止时间: 至
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/6825576
• 关键词: Pneumocystis carinii; Pneumocystis pneumonia; clinical research; diagnosis design /evaluation; diagnostic respiratory lavage; fluorescence resonance energy transfer; gene targeting; human subject; mouthwash; noninvasive diagnosis; patient oriented research; polymerase chain reaction; respiratory disorder diagnosis; sputum

Pneumocystis jiroveci (Pneumocystis carinii) is an important cause of pneumonia (PCP) in immunocompromised individuals. The standard approach for diagnosing PCP is a microscopic examination of smears prepared from induced sputum or bronchial alveolar lavage (BAL) samples. Recently, investigators have been designing and testing PCR assays for the detection of P. jiroveci in respiratory samples. Of particular interest is the use of PCR with oral wash samples as a means of detecting P. jiroveci in the respiratory tract. These noninvasive specimens could prove to be of value for use in screening tests to rule out PCP. Microscopic methods are too insensitive to be useful with oral wash samples. The increased sensitivity of the PCR method, however, generates some positive results with samples obtained from patients who are only colonized or infected at a sub-clinical level. A precise quantitative method could help differentiate low level colonization from infection and, consequently, improve the clinical usefulness of PCR performed on oral washes and other respiratory samples. We have developed a rapid quantitative real time PCR assay targeting the MSG genes of P. jiroveci using fluorescence resonance energy transfer (FRET) detection probes for signal detection. A blinded, prospective study has been conducted with collaborators at UCSF to further evaluate the performance of the real time PCR assay in detecting PCP. For samples obtained within one day of the initiation of PCP therapy the sensitivity of oral wash samples with QTD-PCR for detecting PCP was greater than 90%. The results of this study are in press. A second collaborative study with UCSF is underway to attempt to detect P. jiroveci colonization of the upper airways of health care workers after exposure to patients with PCP. Recent work on an improved method for sample processing has demonstrated that use of DTT markedly improves the homogeneity of the processed oral wash material. If, as expected, this results in more reproducable quantitative results the positive and negative predictive values for PCP associated with certain levels of signal should improve considerably. We are initiating testing of a series of samples with the processing modifications to test this hypothesis.

氏肺囊虫（卡氏肺囊虫）是免疫功能低下个体肺炎（PCP）的重要病因。诊断PCP的标准方法是显微镜检查从诱导痰或支气管肺泡灌洗液（BAL）样品中制备的涂片。最近，研究人员一直在设计和测试呼吸样本中检测耶氏疟原虫的PCR方法。特别令人感兴趣的是使用口腔洗涤样品的聚合酶链反应作为检测呼吸道中耶氏疟原虫的手段。这些非侵入性标本可能被证明在筛查试验中排除PCP的使用价值。显微方法太不敏感，不能用于口腔洗液样品。然而，PCR方法的灵敏度提高，对于仅在亚临床水平上定植或感染的患者获得的样本产生了一些阳性结果。精确的定量方法可以帮助区分低水平定植与感染，从而提高对口腔洗液和其他呼吸道样本进行PCR的临床有效性。利用荧光共振能量转移（FRET）检测探针进行信号检测，建立了一种快速定量实时PCR检测法。与UCSF的合作者进行了一项盲法前瞻性研究，以进一步评估实时PCR检测PCP的性能。对于开始PCP治疗1天内获得的样本，QTD-PCR检测口腔洗液样本PCP的灵敏度大于90%。这项研究的结果正在出版中。第二项与加州大学旧金山分校的合作研究正在进行中，目的是检测接触PCP患者后医护人员上呼吸道的罗氏疟原虫定植。