Literature DB >> 1849539

The detection of human cytomegalovirus immediate early antigen in peripheral blood leucocytes.

G Bein1, A Bitsch, J Hoyer, H Kirchner.   

Abstract

Recently, Van der Bij et al. (1988) reported that active human cytomegalovirus (HCMV) infection could be diagnosed by the detection of HCMV immediate early antigen (IEA) directly in the peripheral blood leucocytes of renal transplant recipients. However, the indirect peroxidase technique used resulted in high background staining due to endogenous peroxidase activity and thus the detection of HCMV-IEA positive leucocytes, which are sometimes present in extremely low numbers, was not always reliable. In an attempt to solve this problem, we have evaluated the alkaline phosphatase-anti-alkaline phosphatase (APAAP) technique, immunogold-silver staining (IGSS), and several fixatives. Fixation with acetone: methanol 1:1 in conjunction with the APAAP technique proved to be the most successful method. In 155 blood samples obtained from 44 patients following renal transplantation and from three AIDS patients, the number of positive cells ranged between 1 and 700 out of 400,000 (median 2). In 23 samples from 11 patients (one AIDS patient) at least one positive cell was found. In this series there were no problems with the evaluation since strong positive signals were obtained without any background staining. We therefore recommend the use of this protocol for the rapid and reliable detection of HCMV-IEA in peripheral blood leucocytes.

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Year:  1991        PMID: 1849539     DOI: 10.1016/0022-1759(91)90022-8

Source DB:  PubMed          Journal:  J Immunol Methods        ISSN: 0022-1759            Impact factor:   2.303


  12 in total

1.  Enhanced analytical sensitivity of a quantitative PCR for CMV using a modified nucleic-acid extraction procedure.

Authors:  A Ferreira-Gonzalez; S Yanovich; M R Langley; L A Weymouth; D S Wilkinson; C T Garrett
Journal:  J Clin Lab Anal       Date:  2000       Impact factor: 2.352

2.  Cytomegalovirus antigenemia assay.

Authors:  M van der Giessen; T H The; W J van Son
Journal:  J Clin Microbiol       Date:  1991-12       Impact factor: 5.948

3.  The intracellular localization of human cytomegalovirus DNA in peripheral blood leukocytes during active infections by high-resolution fluorescence in situ hybridization.

Authors:  H Hackstein; H Kirchner; G Jahn; G Bein
Journal:  Arch Virol       Date:  1996       Impact factor: 2.574

4.  Rapid cytomegalovirus pp65 antigenemia assay by direct erythrocyte lysis and immunofluorescence staining.

Authors:  S K Ho; C Y Lo; I K Cheng; T M Chan
Journal:  J Clin Microbiol       Date:  1998-03       Impact factor: 5.948

5.  Fluorescence in situ hybridization with cosmid clones for the detection of human cytomegalovirus DNA in peripheral blood leukocytes.

Authors:  H Hackstein; G Jahn; H Kirchner; G Bein
Journal:  Histochem Cell Biol       Date:  1996-08       Impact factor: 4.304

6.  Factors influencing detection of quantitative cytomegalovirus antigenemia.

Authors:  M Boeckh; P M Woogerd; T Stevens-Ayers; C G Ray; R A Bowden
Journal:  J Clin Microbiol       Date:  1994-03       Impact factor: 5.948

7.  Effect of delayed processing of blood samples on performance of cytomegalovirus antigenemia assay.

Authors:  J Niubò; J L Pérez; A Carvajal; C Ardanuy; R Martín
Journal:  J Clin Microbiol       Date:  1994-04       Impact factor: 5.948

8.  Rapid detection of cytomegalovirus infection in immunocompromised patients.

Authors:  M Degré; G Bukholm; E Holter; F Müller; H Rollag
Journal:  Eur J Clin Microbiol Infect Dis       Date:  1994-08       Impact factor: 3.267

9.  Comparison of several fixation methods for cytomegalovirus antigenemia assay.

Authors:  J L Pérez; M De Oña; J Niubò; H Villar; S Melón; A García; R Martín
Journal:  J Clin Microbiol       Date:  1995-06       Impact factor: 5.948

10.  Comparison of different immunostaining techniques and monoclonal antibodies to the lower matrix phosphoprotein (pp65) for optimal quantitation of human cytomegalovirus antigenemia.

Authors:  G Gerna; M G Revello; E Percivalle; F Morini
Journal:  J Clin Microbiol       Date:  1992-05       Impact factor: 5.948

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