The most important type I IFNs involved in an antiviral response are IFN-α and IFN-β, and it is well known that stimulation of TLR3 and RIG-I with viral RNA results in type I IFN production [[10, 20]]. As our data suggest that TLR3 and RIG-I play a role in the observed synergistic response to RSV and

MDP, we investigated the induction of IFN-β. As type I IFNs are generally regarded as early responders SAHA HDAC in vivo [[21]], we determined the kinetics of IFN-β induction at an early (4 h) and at a late (24 h) time point following stimulation with RSV, MDP, LPS, and both types of Poly(I:C). Infection with RSV, with and without MDP, showed a small increase of IFN-β mRNA compared with unstimulated KU-57788 in vivo cells after 4 h (Fig. 4A) and a strong increase of IFN-β mRNA after 24 h (Fig. 4B). Stimulation with MDP did not induce upregulation of IFN-β at either time point. Although LPS stimulation resulted in a temporary upregulation of IFN-β mRNA after 4 h, IFN-β was downregulated after 24 h, similar to previous observations [[21]]. Both Poly(I:C) HMW and Poly(I:C)-LyoVec LMW induced an upregulation of IFN-β after 4 h and 24 h (Fig. 4B). These data suggest that stimulation with dsRNA results in IFN-β transcription and stimulation with live RSV results in a delayed IFN-β response. Previous studies have shown

that TLR3, RIG-I, and NOD2 are upregulated by type I IFNs in response to Poly(I:C) and viral infection [[22, 23]]. To investigate whether IFN-β induces a transcriptional upregulation of these receptors, quantitative PCR was used to determine the expression levels of TLR3, RIG-I, and NOD2. Human PBMCs were stimulated with RSV, MDP, IFN-β, and both types of Poly(I:C). Stimulation of human PBMCs with RSV, with and without MDP, showed an upregulation of both TLR3 and RIG-I, although the most pronounced C59 cost effect was observed with RIG-I (Fig. 5A). Similar to RSV stimulation, IFN-β, Poly(I:C) HMW, and Poly(I:C)-LyoVec LMW also induced an increase in TLR3 expression

and a stronger increase in RIG-I transcription. In addition to TLR3 and RIG-I, NOD2 was also found to be upregulated after stimulation with all stimuli except MDP (Fig. 5B), suggesting that in this model RSV, Poly(I:C), and IFN-β affect the transcription of TLR3, RIG-I, and NOD2. Our results suggest that RSV infection induces upregulation of NOD2 in an IFN-β dependent manner. Subsequent stimulation of NOD2 with MDP then results in an elevated response in proinflammatory cytokines. As this implies that the order of events is important, we performed an experiment in which we sequentially stimulated PBMCs. Cells were first stimulated with RSV or MDP for 24 h and then subsequently stimulated with either RSV or MDP for another 24 h. The amount of cytokine release after these stimulations can be found in Supporting Information Fig. 3.