Interferon type III explained

The type III interferon group is a group of anti-viral cytokines, that consists of four IFN-λ (lambda) molecules called IFN-λ1, IFN-λ2, IFN-λ3 (also known as IL29, IL28A and IL28B respectively), and IFN-λ4.[1] They were discovered in 2003.[2] Their function is similar to that of type I interferons, but is less intense and serves mostly as a first-line defense against viruses in the epithelium.[3]

Genomic location

Genes encoding this group of interferons are all located on the long arm of chromosome 19 in human, specifically in region between 19q13.12 and 19q13.13. The IFNL1 gene, encoding IL-29, is located downstream of IFNL2, encoding IL-28A. IFNL3, encoding IL28B, is located downstream of IFNL4.[4]

In mice, the genes encoding for type III interferons are located on chromosome 7 and the family consists only of IFN-λ2 and IFN-λ3.[5]

Structure

Interferons

All interferon groups belong to class II cytokine family which have a conserved structure that comprises six α-helices.[6] The proteins of type III interferon group are highly homologous and show high amino acid sequence similarity between. The similarity between IFN-λ2 and IFN-λ3 is approximately 96%, similarity of IFNλ1 to IFNλ 2/3 is around 81%.[2] Lowest similarity is found between IFN-λ4 and IFN-λ3 - only around 30%.[7] [8] Unlike type I interferon group, which consist of only one exon, type III interferons consist of multiple exons.[9]

Receptor

The receptors for these cytokines are also structurally conserved. The receptors have two type III fibronectin domains in their extracellular domain. The interface of these two domains forms the cytokine binding site. The receptor complex for type III interferons consists of two subunits - IL10RB (also called IL10R2 or CRF2-4) and IFNLR1 (formerly called IL28RA, CRF2-12).[10]

In contrast to the ubiquitous expression of receptors for type I interferons, IFNLR1 is largely restricted to tissues of epithelial origin.[2] [11] Despite high homology between type III interferons, the binding affinity to IFNLR1 differ, with IFN-λ1 showing the highest binding affinity, and IFN-λ3 showing the lowest binding affinity.[8]

Signalling pathway

IFN-λ production is induced by pathogen sensing through pattern recognition receptors (PRR), including TLR, Ku70 and RIG-I-like. The main producer of IFN-λ are type 2 myeloid dendritic cells.

IFN-λ binds to IFNLR1 with a high affinity, which then recruits the low-affinity subunit of the receptor, IL10Rb. This interaction creates a signalling complex. Upon binding of the cytokine to the receptor, JAK-STAT signalling pathway gets activated, specifically JAK1 and TYK2 and phosphorylate and activate STAT-1 and STAT-2, which then induces downstream signalling that leads to induction of expression of hundreds of IFN-stimulated genes (ISG), e.g.: NF-κB, IRF, ISRE, Mx1, OAS1.

The signalling is modulated by suppressor of cytokine signalling 1 (SOCS1) and ubiquitin-specific peptidase 18 (USP18).

Function

Functions of type III interferons overlap largely with that of type I interferons. Both of these cytokine groups modulate the immune response after a pathogen has been sensed in the organism, their functions are mostly anti-viral and anti-proliferative. However, type III interferons tend to be less inflammatory and show a slower kinetics than type I. Also, because of the restricted expression of IFNLR1, the immunomodulatory effect of type III interferons is limited.[12]

Because the receptors for type I and type II interferons are expressed on almost all nucleated cells, their function is rather systemic. Type III interferon receptors are expressed more specifically on epithelial cells and some immune cells such as neutrophils, and depending on the species, B cells and dendritic cells as well.[13] [14] [15] Therefore, their antiviral effects are most prominent in barriers, in gastrointestinal, respiratory and reproductive tracts. Type III interferons usually act as the first line of defense against viruses at the barriers.[16]

In the gastrointestinal tract, both type I and type III interferons are needed to effectively fight reovirus infection. Type III interferons restrict the initial replication of the virus and diminish the shedding of through feces, while type I interferons prevent the systematic infection. On the other hand, in the respiratory tract these two groups of interferons seem to be rather redundant, as documented by the susceptibility of double-deficient mice (in receptors for type I and type III interferons), but the resistance to respiratory virus in mice that are deficient in either type I or type III interferon receptors. Additional gastrointestinal viruses such as rotavirus and norovirus, as well as non-gastrointestinal viruses like influenza and West Nile virus, are also restricted by type III interferons.[17]

Notes and References

  1. Vilcek J . Novel interferons . Nature Immunology . 4 . 1 . 8–9 . January 2003 . 12496969 . 10.1038/ni0103-8 . 32338644 .
  2. Kotenko SV, Gallagher G, Baurin VV, Lewis-Antes A, Shen M, Shah NK, Langer JA, Sheikh F, Dickensheets H, Donnelly RP . 6 . IFN-lambdas mediate antiviral protection through a distinct class II cytokine receptor complex . Nature Immunology . 4 . 1 . 69–77 . January 2003 . 12483210 . 10.1038/ni875 . 2734534 .
  3. Kotenko SV, Durbin JE . Contribution of type III interferons to antiviral immunity: location, location, location . The Journal of Biological Chemistry . 292 . 18 . 7295–7303 . May 2017 . 28289095 . 5418032 . 10.1074/jbc.R117.777102 . free .
  4. Zhou JH, Wang YN, Chang QY, Ma P, Hu Y, Cao X . Type III Interferons in Viral Infection and Antiviral Immunity . english . Cellular Physiology and Biochemistry . 51 . 1 . 173–185 . 2018 . 30439714 . 10.1159/000495172 . free .
  5. Lazear HM, Schoggins JW, Diamond MS . Shared and Distinct Functions of Type I and Type III Interferons . Immunity . 50 . 4 . 907–923 . April 2019 . 30995506 . 6839410 . 10.1016/j.immuni.2019.03.025 .
  6. Renauld JC . Class II cytokine receptors and their ligands: key antiviral and inflammatory modulators . Nature Reviews. Immunology . 3 . 8 . 667–76 . August 2003 . 12974481 . 10.1038/nri1153 . 1229288 .
  7. O'Brien TR, Prokunina-Olsson L, Donnelly RP . IFN-λ4: the paradoxical new member of the interferon lambda family . Journal of Interferon & Cytokine Research . 34 . 11 . 829–38 . November 2014 . 24786669 . 4217005 . 10.1089/jir.2013.0136 .
  8. Fox BA, Sheppard PO, O'Hara PJ . The role of genomic data in the discovery, annotation and evolutionary interpretation of the interferon-lambda family . PLOS ONE . 4 . 3 . e4933 . 2009-03-20 . 19300512 . 2654155 . 10.1371/journal.pone.0004933 . 2009PLoSO...4.4933F . free .
  9. Syedbasha M, Egli A . Interferon Lambda: Modulating Immunity in Infectious Diseases . Frontiers in Immunology . 8 . 119 . 2017-02-28 . 28293236 . 5328987 . 10.3389/fimmu.2017.00119 . free .
  10. Bartlett NW, Buttigieg K, Kotenko SV, Smith GL . Murine interferon lambdas (type III interferons) exhibit potent antiviral activity in vivo in a poxvirus infection model . The Journal of General Virology . 86 . Pt 6 . 1589–1596 . June 2005 . 15914836 . 10.1099/vir.0.80904-0 . free .
  11. Sheppard P, Kindsvogel W, Xu W, Henderson K, Schlutsmeyer S, Whitmore TE, Kuestner R, Garrigues U, Birks C, Roraback J, Ostrander C, Dong D, Shin J, Presnell S, Fox B, Haldeman B, Cooper E, Taft D, Gilbert T, Grant FJ, Tackett M, Krivan W, McKnight G, Clegg C, Foster D, Klucher KM . 6 . IL-28, IL-29 and their class II cytokine receptor IL-28R . Nature Immunology . 4 . 1 . 63–8 . January 2003 . 12469119 . 10.1038/ni873 . 35764259 .
  12. Wack A, Terczyńska-Dyla E, Hartmann R . Guarding the frontiers: the biology of type III interferons . Nature Immunology . 16 . 8 . 802–9 . August 2015 . 26194286 . 7096991 . 10.1038/ni.3212 .
  13. Broggi. Achille. Tan. Yunhao. Granucci. Francesca. Zanoni. Ivan. October 2017. IFN-λ suppresses intestinal inflammation by non-translational regulation of neutrophil function. Nature Immunology. 18. 10. 1084–1093. 10.1038/ni.3821. 1529-2916. 5701513. 28846084.
  14. Hemann EA, Green R, Turnbull JB, Langlois RA, Savan R, Gale M . Interferon-λ modulates dendritic cells to facilitate T cell immunity during infection with influenza A virus . Nature Immunology . 20 . 8 . 1035–1045 . August 2019 . 31235953 . 10.1038/s41590-019-0408-z . 6642690 .
  15. Santer DM, Minty GE, Golec DP, Lu J, May J, Namdar A, Shah J, Elahi S, Proud D, Joyce M, Tyrrell DL, Houghton M . 6 . Differential expression of interferon-lambda receptor 1 splice variants determines the magnitude of the antiviral response induced by interferon-lambda 3 in human immune cells . PLOS Pathogens . 16 . 4 . e1008515 . April 2020 . 32353085 . 7217487 . 10.1371/journal.ppat.1008515 . free .
  16. Lazear HM, Nice TJ, Diamond MS . Interferon-λ: Immune Functions at Barrier Surfaces and Beyond . Immunity . 43 . 1 . 15–28 . July 2015 . 26200010 . 4527169 . 10.1016/j.immuni.2015.07.001 .
  17. Ingle H, Peterson ST, Baldridge MT . Distinct Effects of Type I and III Interferons on Enteric Viruses . Viruses . 10 . 1 . January 2018 . 46 . 29361691 . 5795459 . 10.3390/v10010046 . free .