Imperial College London

DrJamesPease

Faculty of MedicineNational Heart & Lung Institute

Reader in Leukocyte Biology
 
 
 
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Contact

 

+44 (0)20 7594 3162j.pease Website

 
 
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Location

 

109Sir Alexander Fleming BuildingSouth Kensington Campus

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Summary

 

Publications

Citation

BibTex format

@article{Pontejo:2018:10.1159/000492161,
author = {Pontejo, S and Murphy, P and Pease, JE},
doi = {10.1159/000492161},
journal = {Journal of Innate Immunity},
pages = {465--478},
title = {Chemokine subversion by human herpesviruses},
url = {http://dx.doi.org/10.1159/000492161},
volume = {10},
year = {2018}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - Viruses use diverse molecular mechanisms to exploit and evade the immune response. Herpesviruses, in particular, encode functional chemokine and chemokine receptor homologs pirated from the host, as well as secreted chemokine-binding proteins with unique structures. Multiple functions have been described for herpesvirus chemokine components, including attraction of target cells, blockade of leukocyte migration, and modulation of gene expression and cell entry by the virus. Here we review current concepts about how human herpesvirus chemokines, chemokine receptors, and chemokine-binding proteins may be used to shape a proviral state in the host.
AU - Pontejo,S
AU - Murphy,P
AU - Pease,JE
DO - 10.1159/000492161
EP - 478
PY - 2018///
SN - 1662-811X
SP - 465
TI - Chemokine subversion by human herpesviruses
T2 - Journal of Innate Immunity
UR - http://dx.doi.org/10.1159/000492161
UR - https://www.karger.com/Article/FullText/492161
UR - http://hdl.handle.net/10044/1/62688
VL - 10
ER -