CX3CR1 is an important surface molecule for respiratory syncytial virus infection in human airway epithelial cells

Author:

Chirkova Tatiana1,Lin Songbai1,Oomens Antonius G. P.2,Gaston Kelsey A.1,Boyoglu-Barnum Seyhan1,Meng Jia1,Stobart Christopher C.1,Cotton Calvin U.3,Hartert Tina V.4,Moore Martin L.1,Ziady Assem G.1,Anderson Larry J.1

Affiliation:

1. Department of Pediatrics and Children's Healthcare of Atlanta, Emory University, Atlanta, Georgia, USA

2. Center for Veterinary Health Sciences, Oklahoma State University, Stillwater, Oklahoma, USA

3. Division of Pediatric Pulmonology, Case Western University, Cleveland, Ohio, USA

4. Division of Allergy, Pulmonary, and Critical Care Medicine, Department of Medicine and Vanderbilt Center for Asthma and Environmental Health Sciences Research, Vanderbilt University, Nashville, Tennessee, USA

Publisher

Microbiology Society

Subject

Virology

Reference74 articles.

1. Microneutralization test for respiratory syncytial virus based on an enzyme immunoassay;Anderson;J Clin Microbiol,1985

2. CX3CL1-CX3CR1 interaction prevents carbon tetrachloride-induced liver inflammation and fibrosis in mice;Aoyama;Hepatology,2010

3. CX3CR1+ CD8alpha+ dendritic cells are a steady-state population related to plasmacytoid dendritic cells;Bar-On;Proc Natl Acad Sci U S A,2010

4. Predominance of Th2 cytokines, CXC chemokines and innate immunity mediators at the mucosal level during severe respiratory syncytial virus infection in children;Bermejo-Martin;Eur Cytokine Netw,2007

5. Functions of cell surface heparan sulfate proteoglycans;Bernfield;Annu Rev Biochem,1999

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