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Progressive multifocal leukoencephalopathy diagnosed by amplification of JC virus‐specific DNA from cerebrospinal fluid

 

作者: Thomas Weber,   Rodney Turner,   Stephan Frye,   Wolfgang Lüke,   Hans Kretzschmar,   Wilfried Lüer,   Gerhard Hunsmann,  

 

期刊: AIDS  (OVID Available online 1994)
卷期: Volume 8, issue 1  

页码: 49-58

 

ISSN:0269-9370

 

年代: 1994

 

出版商: OVID

 

关键词: JC virus;simian virus 40;polymerase chain reaction;AIDS;HIV-1;progressive multifocal leukoencephalopathy;cerebrospinal fluid;non-invasive diagnosis;immunocytochemistry

 

数据来源: OVID

 

摘要:

ObjectiveTo study the diagnostic sensitivity and specificity of polymerase chain reaction (PCR) for the non-invasive diagnosis of progressive multifocal leukoencephalopathy (PML) in HIV-1-infected individuals.DesignRetrospective analysis of stored cerebrospinal fluid (CSF) samples by PCR of HIV-1-infected patients.MethodsResults of the PCR analysis of the CSF of three AIDS patients with autopsy-proven PML were compared with the results in 15 neurologically asymptomatic HIV-1-infected patients and with 15 AIDS patients with other opportunistic infections of the central nervous system (CNS). A polyclonal antiserum to simian virus 40 (SV40) cross-reacting with JC virus (JCV) late antigens was used for immunocytochemical confirmation of the diagnosis. Two different primer pairs, one taken from the VP1/large T gene and the other from the large T gene, were used to amplify JCV-specific DNA sequences from CSF.ResultsFive CSF samples were analysed and JCV-specific DNA found in three patients with autopsy-proven PML. No JCV-specific DNA was detected in 47 CSF samples, including serial samples from 14 of the 30 non-PML patients. The diagnosis of PML was confirmed in all three cases by immunocytochemistry.Conclusion:PML can be diagnosed by PCR analysis of CSF. The sensitivity and specificity of the method depends on the sensitivity of the primers used for amplification. Using a primer pair from the large T gene, JCV-specific DNA was amplified in three cases with PML as early as the day of presentation with the first neurological symptom of PML.

 

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