Type I IFNs |
IFN‐α |
IFN‐α1, ‐α2, ‐α4, ‐α5, ‐α6, ‐α7, ‐α8, ‐α10, ‐α13, ‐α14, ‐α16, ‐α17, ‐α21 |
IFN‐αR1/IFN‐αR2 |
IFN‐α is primarily produced by pDCs |
Cella et al (1999), Barchet et al (2002), Dai et al (2004), Hardy et al (2004), Jaks et al (2007) |
IFN‐β |
|
IFN‐αR1/IFN‐αR2 |
IFN‐β is produced by most infected cells |
Platanias (2005), Khaitov et al (2009), Ioannidis et al (2013) |
IFN‐ε |
|
IFN‐αR1/IFN‐αR2 |
IFN‐ε is associated with the female reproductive tract |
Fung et al (2013), Marks et al (2019) |
IFN‐κ |
|
IFN‐αR1/IFN‐αR2 |
IFN‐κ is selectively expressed in keratinocytes |
LaFleur et al (2001) |
IFN‐ω |
|
IFN‐αR1/IFN‐αR2 |
One of the least studied IFNs but the presence of neutralizing auto‐antibodies against it in severe COVID‐19 patients suggests its role in antiviral immunity may be underappreciated |
Hauptmann and Swetly (1985), Bastard et al (2020) |
Type II IFNs |
IFN‐γ |
|
IFN‐γR1/ IFN‐γR2 |
Not discussed here |
|
Type III IFNs |
IFN‐λ |
IFN‐λ1, ‐λ2, ‐λ3, ‐λ4 |
IFN‐λR1/IL‐10R2 |
IFN‐λ is produced by infected cells at barrier tissues such as epithelial cells in the respiratory tract |
Meager et al (2005), Sommereyns et al (2008), Jewell et al (2010), Mordstein et al (2010), Crotta et al (2013), Wack et al (2015), Ye et al (2019) |