Imperial College London

ProfessorPaulFarrell

Faculty of MedicineDepartment of Infectious Disease

Professor of Tumour Virology
 
 
 
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Contact

 

+44 (0)20 7594 2005p.farrell Website

 
 
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Location

 

Section of VirologyNorfolk PlaceSt Mary's Campus

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Summary

 

Publications

Citation

BibTex format

@article{Wongwiwat:2022:10.1128/jvi.00394-22,
author = {Wongwiwat, W and Fournier, B and Bassano, I and Bayoumy, A and Elgueta, Karstegl C and Styles, C and Bridges, R and Lenoir, C and BoutBoul, D and Moshous, D and Neven, B and Kanda, T and Morgan, R and White, R and Latour, S and Farrell, P},
doi = {10.1128/jvi.00394-22},
journal = {Journal of Virology},
pages = {1--15},
title = {Epstein-Barr virus genome deletions in Epstein-Barr virus-positive T/NK cell lymphoproliferative diseases},
url = {http://dx.doi.org/10.1128/jvi.00394-22},
volume = {96},
year = {2022}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - The main target cells for Epstein-Barr virus (EBV) infection and persistence are B lymphocytes, although T and NK cells can also become infected. In this paper we characterise the EBV present in 21 pediatric and adult patients treated in France for a range of diseases that involve infection of T or NK cells. Of these 21 cases, 5 pediatric patients (21%) and 11 adult patients (52%) are of Caucasian origin. In about 30% of the cases, some of the EBV genomes contain a large deletion. The deletions are different in every patient but tend to cluster near the BART region of the viral genome. Detailed investigation of a family, in which several members have persistent T or NK cell infection by EBV, indicates that the virus genome deletions arise or are selected independently in each individual patient. Genome sequence polymorphisms in the EBV in these T or NK cell diseases reflect the geographic origin of the patient, not a distinct type of EBV (the 21 cases studied included examples of both type 1 and type 2 EBV infection). Using virus produced from type 1 or type 2 EBV genomes cloned in bacterial artificial chromosome (BAC) vectors, we demonstrate infection of T cells in cord blood from healthy donors. Our results are consistent with transient infection of some T cells being part of normal asymptomatic infection by EBV in young children.
AU - Wongwiwat,W
AU - Fournier,B
AU - Bassano,I
AU - Bayoumy,A
AU - Elgueta,Karstegl C
AU - Styles,C
AU - Bridges,R
AU - Lenoir,C
AU - BoutBoul,D
AU - Moshous,D
AU - Neven,B
AU - Kanda,T
AU - Morgan,R
AU - White,R
AU - Latour,S
AU - Farrell,P
DO - 10.1128/jvi.00394-22
EP - 15
PY - 2022///
SN - 0022-538X
SP - 1
TI - Epstein-Barr virus genome deletions in Epstein-Barr virus-positive T/NK cell lymphoproliferative diseases
T2 - Journal of Virology
UR - http://dx.doi.org/10.1128/jvi.00394-22
UR - https://journals.asm.org/doi/epub/10.1128/jvi.00394-22
UR - http://hdl.handle.net/10044/1/96848
VL - 96
ER -