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. 2019 Apr 1;4(6):914–924. doi: 10.1038/s41564-019-0421-x

Fig. 3. Hypothetical models of different transcriptional outputs in response to viral infection.

Fig. 3

During viral infection, differential IFN signalling inputs may manifest as differences in the magnitude of induced ISGs (a), kinetics of ISG transcription and degradation (b) or composition of ISGs expressed in the transcriptional profile (c). These variations, or a combination thereof, appear to play a significant role in cell-, virus- and species-specific antiviral responses.