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通过聚合酶链反应快速检测支气管肺泡灌洗液和血清样本中的巨细胞病毒:人类免疫缺陷病毒感染患者的病毒分离与临床结局的相关性

Rapid detection of cytomegalovirus in bronchoalveolar lavage fluid and serum samples by polymerase chain reaction: correlation of virus isolation and clinical outcome for patients with human immunodeficiency virus infection.

作者信息

Hansen K K, Vestbo J, Benfield T, Lundgren J D, Mathiesen L R

机构信息

Department of Infectious Diseases, Hvidovre Hospital, Copenhagen, Denmark.

出版信息

Clin Infect Dis. 1997 May;24(5):878-83. doi: 10.1093/clinids/24.5.878.

Abstract

Bronchoalveolar lavage (BAL) fluids and serum samples from 153 patients with pulmonary symptoms who were infected with human immunodeficiency virus (HIV) and underwent BAL were examined for the presence of cytomegalovirus (CMV) by conventional culture and by polymerase chain reaction (PCR) for detection of CMV DNA. PCR detected CMV more frequently than did cultures of BAL fluid (PCR of BAL fluid, 53%; PCR of serum, 40%; and culture, 30%). In a multivariate model, development of extrapulmonary CMV disease was predicted by the finding of CMV in BAL fluid by culture (relative risk [RR], 8.0; confidence interval [CI], 3.8-16.8) or the finding of CMV DNA in serum (RR, 7.4; CI, 3.2-17.3) or BAL fluid (RR, 8.0; CI, 3.1-20.7) by PCR. Mortality was found to be similar for patients who did or did not have CMV detected by either culture or PCR. Detection of CMV DNA by PCR was a more rapid and sensitive technique than conventional culture. Detection of CMV DNA in BAL fluid or serum predicted subsequent development of extrapulmonary CMV disease but not death for HIV-infected patients with pulmonary symptoms.

摘要

对153例有肺部症状且感染了人类免疫缺陷病毒(HIV)并接受支气管肺泡灌洗(BAL)的患者的支气管肺泡灌洗(BAL)液和血清样本,采用传统培养法及聚合酶链反应(PCR)检测巨细胞病毒(CMV)DNA,以检查CMV的存在情况。PCR检测到CMV的频率高于BAL液培养(BAL液PCR检测为53%;血清PCR检测为40%;培养法为30%)。在多变量模型中,通过培养法在BAL液中发现CMV(相对危险度[RR],8.0;置信区间[CI],3.8 - 16.8),或通过PCR在血清(RR,7.4;CI,3.2 - 17.3)或BAL液(RR,8.0;CI,3.1 - 20.7)中发现CMV DNA,可预测肺外CMV疾病的发生。发现通过培养法或PCR检测到或未检测到CMV的患者死亡率相似。与传统培养法相比,PCR检测CMV DNA是一种更快速、灵敏的技术。在有肺部症状的HIV感染患者中,检测BAL液或血清中的CMV DNA可预测随后肺外CMV疾病的发生,但不能预测死亡情况。

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