Resumen
Chemokines and their receptors function in the recruitment and activation of cells of the immune system to sites of inflammation. As such, chemokines play an important role in mediating pathophysiological events during microbial infection. In particular, CXCL9, CXCL10 and CXCL11 and their cognate receptor CXCR3 have been associated with the clinical course of several infectious diseases, including severe acute respiratory syndrome (SARS) and influenza. While CXCL9, CXCL10 and CXCL11 share the same receptor and have overlapping functions, each can also have unique activity in host defense. The lack of a preferred characterized animal model for SARS has brought our attention to ferrets, which have been used for years in influenza studies. The lack of immunological reagents for ferrets prompted us to clone CXCL9, CXCL10, CXCL11 and CXCR3 and, in the case of CXCL10, to express the gene as a recombinant protein. In this study we demonstrate that endogenous ferret CXCL10 exhibits similar mRNA expression patterns in the lungs of deceased SARS patients and ferrets experimentally infected with SARS coronavirus. This study therefore represents an important step towards development of the ferret as a model for the role of CXCL9, CXCL10 and CXCL11:CXCR3 axis in severe viral infections.
Idioma original | English |
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Páginas (desde-hasta) | 1288-1297 |
Número de páginas | 10 |
Publicación | Molecular Immunology |
Volumen | 45 |
N.º | 5 |
DOI | |
Estado | Published - mar. 2008 |
Publicado de forma externa | Sí |
Nota bibliográfica
Funding Information:We thank Feseha Abebe-Akele for technical assistance. This project was supported by funding from NIAID through NIH/NIAID Contract No. N01-AI-30063 Task Order No. 03.
ASJC Scopus Subject Areas
- Immunology
- Molecular Biology
PubMed: MeSH publication types
- Journal Article
- Research Support, N.I.H., Extramural