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A human coronavirus responsible for the common cold massively kills dendritic cells but not monocytes.
Mesel-Lemoine M., Millet J., Vidalain P.-O., Law H., Vabret A., Lorin V., Escriou N., Albert M. L., Nal B., Tangy F.
Journal of Virology 86, 14 (2012) 7577-87 - http://hal-riip.archives-ouvertes.fr/pasteur-00721361
(22553325)
A human coronavirus responsible for the common cold massively kills dendritic cells but not monocytes.
Mariana Mesel-Lemoine1, Jean Millet2, 3, Pierre-Olivier Vidalain1, Helen Law4, Astrid Vabret5, Valérie Lorin1, Nicolas Escriou1, Matthew L Albert4, Béatrice Nal2, 3, Frédéric Tangy () 1
1 :  Génomique Virale et Vaccination
Institut Pasteur de Paris – CNRS : URA3015
25-28 rue du Docteur Roux, F-75724 Paris Cedex 15
France
2 :  Centre de recherche Université de Hong-Kong-Pasteur
http://www.hkupasteur.hku.hk/
Centre de Recherche Université de Hong-Kong-Pasteur – Réseau International des Instituts Pasteur
Hong Kong University Pasteur Research Centre - 1/F Dexter HC Man Building 8, Sassoon Road Pokfulam
Hong-Kong
3 :  Department of Anatomy [HKU]
University of Hong Kong
Hong Kong
Chine
4 :  Immunobiologie des Cellules Dendritiques
INSERM : U818 – Institut Pasteur de Paris
25-28 rue du Docteur Roux, F-75724 Paris Cedex 15
France
5 :  Laboratoire de Virologie
CHU Caen – Université de Caen Basse-Normandie
France
Human coronaviruses are associated with upper respiratory tract infections that occasionally spread to the lungs and other organs. Although airway epithelial cells represent an important target for infection, the respiratory epithelium is also composed of an elaborate network of dendritic cells (DCs) that are essential sentinels of the immune system, sensing pathogens and presenting foreign antigens to T lymphocytes. In this report, we show that in vitro infection by human coronavirus 229E (HCoV-229E) induces massive cytopathic effects in DCs, including the formation of large syncytia and cell death within only few hours. In contrast, monocytes are much more resistant to infection and cytopathic effects despite similar expression levels of CD13, the membrane receptor for HCoV-229E. While the differentiation of monocytes into DCs in the presence of granulocyte-macrophage colony-stimulating factor and interleukin-4 requires 5 days, only 24 h are sufficient for these cytokines to sensitize monocytes to cell death and cytopathic effects when infected by HCoV-229E. Cell death induced by HCoV-229E is independent of TRAIL, FasL, tumor necrosis factor alpha, and caspase activity, indicating that viral replication is directly responsible for the observed cytopathic effects. The consequence of DC death at the early stage of HCoV-229E infection may have an impact on the early control of viral dissemination and on the establishment of long-lasting immune memory, since people can be reinfected multiple times by HCoV-229E.
Sciences du Vivant/Microbiologie et Parasitologie/Virologie
Anglais
1098-5514

Articles dans des revues avec comité de lecture
10.1128/JVI.00269-12
Journal of Virology (J Virol)
Publisher American Society for Microbiology
ISSN 0022-538X 
internationale
07/2012
02/05/2012
86
14
7577-87