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巨细胞病毒即刻早期mRNA测定在肾移植后巨细胞病毒感染中的诊断价值 被引量:4

Diagnostic implication of human cytomegalovirus immediate early 1 mRNA detection by nucleic acid sequence-based amplification in renal transplant recipients
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摘要 目的评价应用核酸基础序列扩增法(NASBA)检测巨细胞病毒(CMV)即刻早期(IE)mRNA对肾移植术后CMV活动性感染的诊断价值。方法采用NASBA法测定55例肾移植患者的外周血标本中CMVIE mRNA及pp67mRNA,免疫组化法检测CMV pp65抗原。结果55例患者中,发生有症状的CMV活动性感染者13例;IE mRNA阳性者20例,12例有CMV活动性感染,IE mRNA的敏感度、特异度、阳性预测值及阴性预测值分别为92.3%、80.9%、60.0%及97.1%。IE mRNA阳性结果出现最早,为术后(31.0±15.4)d,与pp67mRNA的(43.7±16.3)d和pp65抗原的(39.6±15.6)d相比,差异有统计学意义(P<0.05)。结论应用NASBA法检测CMV IEmRNA,能够早期、快速、准确的诊断CMV活动性感染,为临床抗病毒的治疗提供依据。 Objective To evaluate the significance of immediate early 1 (IE) mRNA detection by nucleic acid sequence-based amplification (NASBA) in the diagnosis of human cytomegalovirus (HCMV) infection after renal transplantation. Methods The expression of IE-mRNA and pp67-mRNA was detected by NASBA in 55 patients after renal transplantation, and pp65 antigenemia assays were done for all cases. Results Twenty cases were positive for IE-mRNA. Thirteen cases were suffered from CMV disease with symptoms. The sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) of IE-mRNA by NASBA were 92. 3%, 80. 9%, 60. 0% and 97. 1%, respectively. Time to first IE-mRNA positive detection after transplantation was shortest, compared with pp67 and antigenemia (P〈0. 05). Conclusion Detection of IE-mRNA using NASBA presents an early, convenient and credible approach for the diagnosis of CMV infection after renal transplantation.
出处 《中华器官移植杂志》 CAS CSCD 北大核心 2005年第11期669-671,共3页 Chinese Journal of Organ Transplantation
基金 广东省科委科技攻关项目(2003c31203) 广东省自然科学基金资助(960131)
关键词 肾移植 巨细胞病毒感染 基因扩增 Kidney transplantation Cytomegalovirus infections Gene amplification
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参考文献5

  • 1陈俊星,郑克立,朱兰英,陈立中,王长希,徐鸿绪,费继光.pp67-mRNA在移植术后人巨细胞病毒感染中的诊断价值[J].中华器官移植杂志,2004,25(2):111-113. 被引量:6
  • 2Greijer, Verschuuren, Dekkers, et al. Expression dynamics of human cytomegalovirus immuevasion genes US3, US6, and US11 in the blood of transplant recipients. J Infect Dis, 2001, 184:247-255.
  • 3Goossens, Christiaans, Blok, et al. Onset and duration of cytomegalovirus immediate-early 1 mRNA expression in the blood of renal transplant recipients. J Med Virol, 2004, 72:94-101.
  • 4Mengoli, Cusinato, Biasolo, et al. Assessment of CMV load in solid organ transplant recipients by pp65 antigenemia and real-time quantitative DNA PCR assay: correlation with pp67 RNA detection. J Med Virol, 2004, 74:78-84.
  • 5Gerna, Baldanti, Lilleri, et al, Human cytomegalovirus pp67 mRNAemia versus pp65 antigenemia for guiding preemptive therapy in heart lung transplant recipients:a prospective,random controlled, open-label trial. Transplantation, 2003, 75: 1012-1019.

二级参考文献4

  • 1Middeldorp JM, Sillekens P, Lunenberg J, et al. Diagnosis of active HCMV infection: the mRNA approach. Organs And Tissues, 2000,2:99-107.
  • 2Boom R, Sol CJA, Salimans MMM, et al. Rapid and simple method for purification of nucleic acids. J Clin Microbiol, 1990, 28:495-503.
  • 3Zhang E, Tetalis, Wang XP, et al. Detection of cytomegalovirus pp67 late gene transcripts in cerebrospinal fluid of human immuodeficiency virus type l-infected patients by nucleic acid sequence-based amplification. J Clin Microbiol, 2000, 38:1920-1925.
  • 4Middeldorp JM. Direct quantitation of human cytomegalovirus (HCMV) immediate early and late mRNA levels in the blood of HCMV infected individuals using competitive NASBA. J Clin Virol,1999,12:103-106.

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