SARS-CoV and IFN: Too Little, Too Late.
Identifieur interne : 000D06 ( PubMed/Curation ); précédent : 000D05; suivant : 000D07SARS-CoV and IFN: Too Little, Too Late.
Auteurs : Eveline Kindler [Suisse] ; Volker Thiel [Suisse]Source :
- Cell host & microbe [ 1934-6069 ] ; 2016.
Descripteurs français
- KwdFr :
- MESH :
- virologie : Poumon.
- Animaux, Interféron de type I, Réplication virale, Virus du SRAS.
English descriptors
- KwdEn :
- MESH :
- chemical : Interferon Type I.
- virology : Lung.
- Animals, SARS Virus, Virus Replication.
Abstract
Dysregulated type I interferon (IFN-I) expression can lead to severe pathology and disease. In this issue of Cell Host & Microbe, Channappanavar et al. (2016) use a SARS-coronavirus animal model to describe how rapid and robust virus replication with delayed IFN-I can lead to lung immunopathology, with fatal outcomes.
DOI: 10.1016/j.chom.2016.01.012
PubMed: 26867172
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pubmed:26867172Le document en format XML
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<front><div type="abstract" xml:lang="en">Dysregulated type I interferon (IFN-I) expression can lead to severe pathology and disease. In this issue of Cell Host & Microbe, Channappanavar et al. (2016) use a SARS-coronavirus animal model to describe how rapid and robust virus replication with delayed IFN-I can lead to lung immunopathology, with fatal outcomes. </div>
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