Interleukin 29

IFNL1
Available structures
PDBHuman UniProt search: PDBe RCSB
Identifiers
AliasesIFNL1, IL-29, IL29, interferon, lambda 1, interferon lambda 1
External IDsOMIM: 607403 HomoloGene: 131189 GeneCards: IFNL1
Orthologs
SpeciesHumanMouse
Entrez

282618

n/a

Ensembl

ENSG00000182393

n/a

UniProt

Q8IU54

n/a

RefSeq (mRNA)

NM_172140

n/a

RefSeq (protein)

NP_742152

n/a

Location (UCSC)Chr 19: 39.3 – 39.3 Mbn/a
PubMed search[2]n/a
Wikidata
View/Edit Human

Interleukin-29 (IL-29) is a cytokine and it belongs to type III interferons group, also termed interferons λ (INF-λ). IL-29 (alternative name INFλ1) plays an important role in the immune response against pathogenes and especially against viruses by mechanisms similar to type I interferons, but targeting primarily cells of epithelial origin and hepatocytes.[3][4]

IL-29 is encoded by the INFL1 gene located on chromosome 19 in humans.[3][5] It is a pseudogene in mice meaning the IL-29 protein is not produced in them.[3]

Structure

IL-29 is, with the rest of INF-λ, structurally related to the IL-10 family, but its primary amino acid sequence (and also function) is more similar to type I interferons.[3] It binds to a heterodimeric receptor composed of one subunit INFL1R specific for INF-λ and a second subunit IL10RB shared among the IL-10 family cytokines.[3]

Function

Effects on immune response to pathogenes  

IL-29 exhibits antiviral effects by inducing similar signaling pathways as type I interferons.[3] IL-29 receptor signals through JAK-STAT pathways leading to activated expression of interferon-stimulated genes and production of antiviral proteins.[6] Further consequences of IL-29 signalization comprise the upregulated expression of MHC class I molecules,[3] or enhanced expression of the costimulatory molecules and chemokine receptors on pDC, which are the main producers of INF-α.[6]

IL-29 expression is dominant in virus-infected epithelial cells of the respiratory, gastrointestinal and urogenital tracts, also in other mucosal tissues and skin. Hepatocytes infected by HCV or HBV viruses stimulate the immune response by producing IL-29 (INF-λ in general) rather than type I interferons.[3][4] It is also produced by maturing macrophages, dendritic cells or mastocytes.[4]

It plays a role in defense against pathogens apart from viruses.[3] It affects the function of both innate and adaptive immune system. Besides described antiviral effects, IL-29 modulates cytokine production of other cells, for example, it increases secretion of IL-6, IL-8 and IL-10 by monocytes and macrophages, enhances the responsiveness of macrophages to IFN-γ by increased expression of IFNGR1, stimulates T cell polarization towards Th1 phenotype and also B cell response to IL-29 was reported.[6]

Antitumor immunity

The impact of IL-29 on cancer cells is complicated and it depends on cancer cell type. It shows protective antitumor effects in many cases such as skin, lung, colorectal or hepatocellular cancer, but it was also reported its protumor effects on multiple myeloma cells.[4] INF-λ are considering as tool in cancer therapy with effects on more restricted cell types and fewer side-effects than type I interferons.[3][4]

Autoimmune diseases

Abnormal expression of IL-29 could be involved in the pathogenesis of the autoimmune diseases by enhancing the production of inflammatory cytokines, chemokines, and other autoimmune‐related components. High levels of IL-29 in serum or disease-specific tissue was observed in patients with rheumatoid arthritis, osteoarthritis, systemic lupus erythematosus, Sjögren's syndrome, psoriasis, atopic dermatitis, Hashimoto's thyroiditis, systemic sclerosis and uveitis.[6]

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000182393 - Ensembl, May 2017
  2. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. 1 2 3 4 5 6 7 8 9 10 Lazear, Helen M.; Nice, Timothy J.; Diamond, Michael S. (2015-07-21). "Interferon-λ: immune functions at barrier surfaces and beyond". Immunity. 43 (1): 15–28. doi:10.1016/j.immuni.2015.07.001. ISSN 1074-7613. PMC 4527169. PMID 26200010.
  4. 1 2 3 4 5 Kelm, Noah E.; Zhu, Ziwen; Ding, Vivi A.; Xiao, Huaping; Wakefield, Mark R.; Bai, Qian; Fang, Yujiang (2016). "The role of IL-29 in immunity and cancer". Critical Reviews in Oncology/Hematology. 106: 91–98. doi:10.1016/j.critrevonc.2016.08.002. ISSN 1879-0461. PMC 7129698. PMID 27637354.
  5. "Entrez Gene: interleukin 29 (interferon".
  6. 1 2 3 4 Wang, Jia‐Min; Huang, An‐Fang; Xu, Wang‐Dong; Su, Lin‐Chong (2019). "Insights into IL‐29: Emerging role in inflammatory autoimmune diseases". Journal of Cellular and Molecular Medicine. 23 (12): 7926–7932. doi:10.1111/jcmm.14697. ISSN 1582-1838. PMC 6850914. PMID 31578802.

Further reading

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