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聚合酶链反应(PCR)与标准细胞学染色法在检测人类免疫缺陷病毒感染患者或高危患者呼吸道标本中卡氏肺孢子虫的比较。

Comparison of PCR and standard cytological staining for detection of Pneumocystis carinii from respiratory specimens from patients with or at high risk for infection by human immunodeficiency virus.

作者信息

Leibovitz E, Pollack H, Moore T, Papellas J, Gallo L, Krasinski K, Borkowsky W

机构信息

Department of Pediatrics, New York University Medical Center, New York 10016, USA.

出版信息

J Clin Microbiol. 1995 Nov;33(11):3004-7. doi: 10.1128/jcm.33.11.3004-3007.1995.

Abstract

The detection of Pneumocystis carinii DNA by PCR was compared with routine cytologic staining techniques (CYT). A total of 284 clinical respiratory specimens, including 137 bronchoalveolar lavage (BAL), 63 bronchoalveolar washing, 63 sputum, and 21 induced sputum samples, obtained from patients with or at high risk for human immunodeficiency virus infection were evaluated. Eighty specimens were positive by PCR, and 69 were positive by CYT. PCR was able to detect P. carinii in more bronchoalveolar washing specimens (15 versus 11) and in comparable BAL specimens (53 versus 54) compared with CYT. PCR was particularly more sensitive than CYT in detecting P. carinii in expectorated sputum (12 versus 4 samples). Of the 19 patients whose respiratory specimens were positive for P. carinii by PCR but negative by CYT, 5 had P. carinii pneumonia (PCP) confirmed by subsequent BAL and transbronchial or mediastinal lymph node biopsy and 9 had a clinical course highly suggestive of acute PCP. Eleven (58%) of the 19 patients with discordant PCR and CYT results had received prior anti-PCP prophylaxis. In this clinical setting in particular and in the evaluation of sputum specimens, the ability of PCR to detect a low parasitic load suggests that this technique may become an important additional tool, along with current cytological methods, for the detection of P. carinii.

摘要

通过聚合酶链反应(PCR)检测卡氏肺孢子虫DNA,并与常规细胞学染色技术(CYT)进行比较。对从人类免疫缺陷病毒感染患者或高危患者获得的总共284份临床呼吸道标本进行了评估,其中包括137份支气管肺泡灌洗(BAL)标本、63份支气管肺泡冲洗标本、63份痰液标本和21份诱导痰液标本。80份标本经PCR检测呈阳性,69份经CYT检测呈阳性。与CYT相比,PCR能够在更多的支气管肺泡冲洗标本(15份对11份)和相当数量的BAL标本(53份对54份)中检测到卡氏肺孢子虫。在检测咳出的痰液中的卡氏肺孢子虫时,PCR比CYT尤其更敏感(12份样本对4份样本)。在19例呼吸道标本经PCR检测卡氏肺孢子虫呈阳性但经CYT检测呈阴性的患者中,5例经随后的BAL以及经支气管或纵隔淋巴结活检确诊为卡氏肺孢子虫肺炎(PCP),9例患者的临床病程高度提示急性PCP。在PCR和CYT结果不一致的19例患者中,11例(58%)曾接受过预防性抗PCP治疗。特别是在这种临床情况下以及在痰液标本的评估中,PCR检测低寄生虫载量的能力表明,该技术可能会成为一种重要的辅助工具,与当前的细胞学方法一起用于检测卡氏肺孢子虫。

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Usefulness of PCR for detection of Pneumocystis carinii DNA.聚合酶链反应检测卡氏肺孢子虫DNA的实用性
J Clin Microbiol. 1994 Sep;32(9):2324-6. doi: 10.1128/jcm.32.9.2324-2326.1994.
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