## Abstract A real‐time polymerase chain reaction assay for quantitation of Epstein‐Barr virus (EBV) DNA in serum was developed. This assay detected EBV DNA in 24 (89%) of 27 sera from patients with infectious mononucleosis, but only in 9 (18%) of 51 sera from EBV carriers (__P__ < 0.001) and in no
Epstein-Barr virus (EBV) DNA levels in palatine tonsils and autologous serum from EBV carriers
✍ Scribed by David Nadal; Martin Blasius; Felix K. Niggli; Gabriela Meier; Christoph Berger
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 83 KB
- Volume
- 67
- Category
- Article
- ISSN
- 0146-6615
- DOI
- 10.1002/jmv.2192
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✦ Synopsis
Abstract
A real‐time polymerase chain reaction was employed to detect and quantitate Epstein‐Barr virus (EBV) DNA in tonsils and autologous sera from EBV‐seropositive children. EBV DNA was found in 95% of tonsils from 21 children and in 50% from 18 children with serum IgG titers to the virus capsid antigen (VCA) of ≥1:160 and 1:10 to 1:80, respectively (P = 0.002). Tonsils from children with titers ≥1:160 harbored more EBV DNA copies per mg tissue (mean, 1,237; range, < 2–13,998) than from children with titers 1:10 to 1:80 (mean, 23; range, < 2–226; P < 0.0001). By contrast, EBV DNA was detected only in serum from 25% of 20 children with titers ≥ 1:160. Thus, ample differences in tonsillar EBV replication are mirrored inconstantly by detectable EBV in autologous serum suggesting that EBV DNA quantitation in tonsils may serve for refined monitoring of individuals at risk of EBV‐associated lymphoproliferation. J. Med. Virol. 67:54–58, 2002. © 2002 Wiley‐Liss, Inc.
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