Article (Scientific journals)
ChemR23 dampens lung inflammation and enhances anti-viral immunity in a mouse model of acute viral pneumonia
Bondue, Benjamin; Vosters, Olivier; de Nadai, Patricia et al.
2011In PLoS Pathogens, 7 (11), p. 1002358
Peer Reviewed verified by ORBi
 

Files


Full Text
ppat.1002358.pdf
Publisher postprint (3.1 MB)
Request a copy

All documents in ORBi are protected by a user license.

Send to



Details



Keywords :
pneumovirus; chemerin; pneumonia
Abstract :
[en] Viral diseases of the respiratory tract, which include influenza pandemic, children acute bronchiolitis, and viral pneumonia of the elderly, represent major health problems. Plasmacytoid dendritic cells play an important role in anti-viral immunity, and these cells were recently shown to express ChemR23, the receptor for the chemoattractant protein chemerin, which is expressed by epithelial cells in the lung. Our aim was to determine the role played by the chemerin/ChemR23 system in the physiopathology of viral pneumonia, using the pneumonia virus of mice (PVM) as a model. Wild-type and ChemR23 knock-out mice were infected by PVM and followed for functional and inflammatory parameters. ChemR23(-/-) mice displayed higher mortality/morbidity, alteration of lung function, delayed viral clearance and increased neutrophilic infiltration. We demonstrated in these mice a lower recruitment of plasmacytoid dendritic cells and a reduction in type I interferon production. The role of plasmacytoid dendritic cells was further addressed by performing depletion and adoptive transfer experiments as well as by the generation of chimeric mice, demonstrating two opposite effects of the chemerin/ChemR23 system. First, the ChemR23-dependent recruitment of plasmacytoid dendritic cells contributes to adaptive immune responses and viral clearance, but also enhances the inflammatory response. Second, increased morbidity/mortality in ChemR23(-/-) mice is not due to defective plasmacytoid dendritic cells recruitment, but rather to the loss of an anti-inflammatory pathway involving ChemR23 expressed by non-leukocytic cells. The chemerin/ChemR23 system plays important roles in the physiopathology of viral pneumonia, and might therefore be considered as a therapeutic target for anti-viral and anti-inflammatory therapies.
Disciplines :
Microbiology
Author, co-author :
Bondue, Benjamin;  Université de Bruxelles
Vosters, Olivier;  Université de bruxelles
de Nadai, Patricia;  Université de bruxelles
Glineur, Stéphanie ;  Université de Liège - ULiège > Département de morphologie et pathologie > Pathologie spéciale et autopsies
De Henau, Olivier;  Université de bruxelles
Luangsay, Souphalone;  Université de bruxelles
Van Gool, Frederic;  Université de bruxelles
Communi, David;  Université de bruxelles
De Vuyst, Paul;  Université de bruxelles
Desmecht, Daniel ;  Université de Liège - ULiège > Département de morphologie et pathologie > Pathologie spéciale et autopsies
Parmentier, Marc
Language :
English
Title :
ChemR23 dampens lung inflammation and enhances anti-viral immunity in a mouse model of acute viral pneumonia
Publication date :
November 2011
Journal title :
PLoS Pathogens
ISSN :
1553-7366
eISSN :
1553-7374
Publisher :
Public Library of Science, San Francisco, United States - California
Volume :
7
Issue :
11
Pages :
e1002358
Peer reviewed :
Peer Reviewed verified by ORBi
Available on ORBi :
since 19 January 2012

Statistics


Number of views
88 (6 by ULiège)
Number of downloads
3 (3 by ULiège)

Scopus citations®
 
77
Scopus citations®
without self-citations
67
OpenCitations
 
63

Bibliography


Similar publications



Contact ORBi