Devi Rajan, Raghavan Chinnadurai, Evan O Keefe, Seyhan Boyoglu-Barnum, Sean O Todd, Tina V Hartert, Jacques Galipeau, Larry J Anderson
Virology 2017 DecRSV is a major cause of severe lower respiratory infection in infants and young children. With no vaccine yet available, it is important to clarify mechanisms of disease pathogenesis. Since indoleamine-2,3-dioxygenase (IDO) is an immunomodulatory enzyme and is upregulated with RSV infection, we studied it in vivo during infection of BALB/c mice and in vitro in A549 cells. RSV infection upregulated IDO transcripts in vivo and in vitro. IDO siRNA decreased IDO transcripts ~2 fold compared to control siRNA after RSV infection but this decrease did not affect RSV replication. In the presence of IFN-γ, siRNA-induced a decrease in IDO expression that was associated with an increase in virus replication and increased levels of IL-6, IL-8, CXCL10 and CCL4. Thus, our results show IDO is upregulated with RSV infection and this upregulation likely participates with IFN-γ in inhibition of virus replication and suppression of some host cell responses to infection. Copyright © 2017 Elsevier Inc. All rights reserved.
Devi Rajan, Raghavan Chinnadurai, Evan O Keefe, Seyhan Boyoglu-Barnum, Sean O Todd, Tina V Hartert, Jacques Galipeau, Larry J Anderson. Protective role of Indoleamine 2,3 dioxygenase in Respiratory Syncytial Virus associated immune response in airway epithelial cells. Virology. 2017 Dec;512:144-150
PMID: 28963880
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