Interleukin 40

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C17orf99
Identifiers
AliasesC17orf99, UNQ464, chromosome 17 open reading frame 99, IL-40, IL40, Interleukin 40
External IDsMGI: 1924977 HomoloGene: 90660 GeneCards: C17orf99
Orthologs
SpeciesHumanMouse
Entrez

100141515

77727

Ensembl

ENSG00000187997

ENSMUSG00000025573

UniProt

Q6UX52

Q9CX63

RefSeq (mRNA)

NM_001163075

NM_029964

RefSeq (protein)

NP_001156547

NP_084240

Location (UCSC)Chr 17: 78.15 – 78.17 MbChr 11: 117.69 – 117.7 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Interleukin 40 (IL-40), also known with other name C17orf99, is a protein belonging to a group of cytokines called interleukins. It is encoded by a gene that does not belong to any cytokine superfamily.[5] This cytokine is produced primarily by human expression tissues such as bone marrow and fetal liver, and its expression can be also induced in peripheral B cells after activation.[6] IL-40 is involved in immunoglobulin A (IgA) production, and plays an important role in humoral immune responses and B cell homeostasis and development.[7][8]

Discovery, genes and expression[edit]

In October 2017, an article was published[9] concerning a previously uncharacterized gene C17orf99 (chromosome 17 open reading frame 99) which is localized on chromosome 17 (17q25.3).[10] This gene encodes a polypeptide chain with 265 amino acids long sequence (including a 20-aa signal peptide), which further determines the mature small secreted protein with predicted molecular weight of approximately 27 kDa.

Due to its unique sequence, IL-40 is not structurally related to any other cytokine family, suggesting that it has a distinct evolutionary history. Besides IL-40, there are few cytokines that also do not belong to any cytokine superfamily, namely: IL-32 and IL-34.[7]

Since this protein is primarily secreted after B cell activation, it was assumed that the gene product C17orf99 would affect the immune system, however, the precise effects require further investigation. Testing was conducted on mice with targeted chromosomal deletion. The novel cytokine that resulted from the study was designated IL-40 and is the most recent in a line of cytokines found.

Only mammalian genomes contain C17orf99, which is expressed by B cells that have been activated, however the expression profile of IL-40 is similar in two species (mouse and human) and is 72% conserved at the amino acid level between them.[9]

Function[edit]

IL-40 has been found is crucial for humoral immune reactions, synthesis of IgA[11] and might be helpful for the growth of B cells, B cell maturation in the BM and in the periphery and their homeostasis. Importantly, human activated B cells and some B cell lymphomas express IL-40 as well. The major producing cells are B cells, bone marrow stroma cells.

IL-40 is associated with lactation and affects initiation of IgA production in the mammary gland. Through the interaction of mucosal immunity and microbiota, the composition of the gut microbiome in mice is also correlated with expression of cytokine IL-40.

Cytokines like IL-4 and TGF-1 can increase the amount of IL-40.

Latter findings imply that it might be related to pathophysiological and inflammatory aspects of diseases.

Clinical significance[edit]

IL-40 cytokine may play a regulatory role in the pathogenesis of inflammatory diseases such as rheumatoid arthritis, ankylosing spondylitis, which is a common chronic inflammatory autoimmune rheumatic disorder, diabetes mellitus,[12] several cell lines of human diffuse large B cell lymphoma and also can play some role in autoimmune hepatitis as discriminating autoantigens.[6]

In a disorder called ankylosing spondylitis (AS),[13] it has been discovered to be connected with elevated circulating levels of pro-inflammatory cytokines and additionally, it has been revealed that anti-inflammatory cytokines are crucial for AS immunological homeostasis such as interleukin (IL)-1 family, in that it includes both pro-inflammatory (IL-1α, IL-1β, IL-18, IL-33, and IL-36) and anti-inflammatory (IL-37 and IL-38) cytokines. It has been revealed that IL-40 was significantly higher in AS patients than in controls, and it can be used as biomarker with other cytokines in serum of patients.[14][15][16]

Rheumatoid Arthritis (RA)[edit]

Given the association of IL-40 with B cells homeostasis[17] and the crucial role of B cells in autoimmunity,[17] it only makes sense to focus on this cytokine during studies of rheumatoid arthritis or autoimmunity in general. Exploring IL-40 as a potential biomarker for earlier diagnosis of these diseases could lead to improvement in therapeutic outcomes. Additionally, there is potential to leverage IL-40 in therapeutic interventions.[18]

The expression of IL-40, an interleukin involved in immune regulation, has been found to be elevated in the synovial fluid of patients with rheumatoid arthritis.[17] RA is characterized by autoimmune reactions primarily targeting the synovial membrane,[19] making the synovial fluid a valuable medium for studying molecules that interact with or originate from this membrane. A comparison of IL-40 expression in synovial tissue between RA and osteoarthritis (OA) patients reveals significantly higher levels in RA patients, particularly within the inflammatory infiltrate. Within the synovial tissue of RA patients, IL-40 is observed to co-localize with various immune cells such as macrophages, B cells, T cells, and neutrophils.[17] Neutrophils, in particular, have been identified as a known source of IL-40 in the context of RA.[17]

In addition to its presence in the synovial fluid, IL-40 levels are elevated in the serum of RA patients compared to those with OA. However, the concentration of IL-40 is notably higher in the local inflammatory sites, specifically the RA synovial fluid, compared to levels of IL-40 in serum.[17][18]

IL-40 in RA patients is correlated with disease activity and the levels of autoantibodies.[17] Furthermore, during the early stages of RA, IL-40 is elevated in the serum compared to healthy individuals. However, after three months of conventional therapy, IL-40 levels in the early stages of RA can be normalized.[18] Studies have shown that elevated IL-40 levels in RA decrease following B-cell depletion therapy, as demonstrated by the effects of rituximab on serum IL-40 after 16 and 24 weeks of therapy [17]

Serum levels of IL-40 in early RA correlate with the levels of autoantibodies and NETosis markers. These correlations become evident when neutrophils are stimulated to undergo NETosis or when they are exposed to inflammatory factors like IL-1β, IL-8, tumor necrosis factor, or lipopolysaccharide. Following the induction of NETosis or exposure to inflammatory cytokines, neutrophils showed enhanced secretion of IL-40, indicating their potential involvement in the heightened IL-40 levels observed among early RA patients.[17][18]

Ankylosing Spondylitis (AS)[edit]

For ankylosing spondylitis (AS) IL-40 has a potential relevance as a biomarker. The levels of IL-40 are significantly higher in the serum of AS patients in comparison with healthy controls (HCs). IL-40 might have excellent diagnostic performance, suggesting its potential as a biomarker for AS susceptibility.[20] IL-40 levels were upregulated in serum of AS patients regardless of age, disease duration, disease activity or HLA-B27.[20] This observation is relevant to AS since it is suggested that the gut microbiota plays a role in the development of the condition.[20]

Type 2 Diabetes Mellitus[edit]

IL-40, an interleukin associated with inflammatory diseases, emerges as a promising candidate in the search for biomarkers linked to type 2 diabetes mellitus (T2DM). In T2DM, a condition characterized by a mild form of inflammation, there is a growing hypothesis suggesting that IL-40 may play a role in its development. Levels of IL-40 in serum of T2DM patients were significantly elevated in comparison to HCs.[12]

What makes these findings particularly compelling is that the observed differences in IL-40 levels remain statistically significant even after accounting for various factors that could potentially influence the results. These factors include age, gender, disease duration and body mass index, diabetic neuropathy, fasting plasma glucose levels, and glycated hemoglobin.[12] Thus, IL-40 not only stands out as an excellent predictor for distinguishing between individuals with T2DM and healthy individuals but also demonstrates its significance as an independent biomarker.[12]

Furthermore, IL-40 levels uncover a negative correlation between IL-40 and both age and age of onset. This relationship suggests that IL-40 may not only serve as a reliable biomarker for distinguishing individuals with T2DM but also provide insights into the progression and onset of the disease.[12] The elevated IL-40 levels found in the serum of T2DM patients present a compelling case for considering IL-40 as a valuable and reliable biomarker in clinical settings, facilitating the identification and differentiation of individuals with T2DM from healthy counterparts.[12]

Sjögren syndrome[edit]

Recently, an implication of IL-40 in the pathogenesis of primary Sjögren syndrome (pSS) and pSS-associated lymphoma was investigated. Overexpression of IL-40 was demonstrated in the salivary glands of patients with pSS, particularly in lymphocytic infiltrates and ductal epithelial cells, when compared to non-Sjögren's syndrome patients (nSS). IL-40 was also up-regulated in patients with pSS-associated lymphoma in comparison to nSS.[21] The expression of IL-40 was associated with the degree of inflammatory infiltrate in the salivary glands,[21] which suggests a potential role of IL-40 in driving the inflammatory response. The tissue expression of IL-40 correlated with the expression levels of IL-4 and TGF-β.[21]

In comparison to nSS patients, CD19+ B lymphocytes were the major source of IL-40 in the lymphatic-infiltrated glands of pSS patients.

[21] Furthermore, pSS patients had an expanded population of CD19+IL-40+ B cells in peripheral blood mononuclear cells compared to HCs.[21] In addition, IL-40 was elevated in the serum of patients with pSS compared to nSS and significantly correlated with the disease activity score EULAR Sjögren’s Syndrome Disease Activity Index. (citace) Moreover, a positive association was found between IL-40 levels and anti-SSA (Sjögren Syndrome related antigen A) and immunoglobulin (Ig) levels.[21] In in vitro conditions, recombinant IL-40 significantly enhanced the expression of proinflacmmatory cytokines in T cells and IFN-γ production by B cells, both isolated from pSS patients.[21] Moreover, recombinant IL-40 stimulated NETosis in neutrophils from pSS patients.[21]

References[edit]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000187997 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000025573 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Zlotnik A (2020-05-15). "Perspective: Insights on the Nomenclature of Cytokines and Chemokines". Frontiers in Immunology. 11: 908. doi:10.3389/fimmu.2020.00908. PMC 7243804. PMID 32499780.
  6. ^ a b Zingaretti C, Arigò M, Cardaci A, Moro M, Crosti M, Sinisi A, et al. (December 2012). "Identification of new autoantigens by protein array indicates a role for IL4 neutralization in autoimmune hepatitis". Molecular & Cellular Proteomics. 11 (12): 1885–1897. doi:10.1074/mcp.M112.018713. PMC 3518104. PMID 22997428.
  7. ^ a b Catalan-Dibene J, McIntyre LL, Zlotnik A (October 2018). "Interleukin 30 to Interleukin 40". Journal of Interferon & Cytokine Research. 38 (10): 423–439. doi:10.1089/jir.2018.0089. PMC 6206549. PMID 30328794.
  8. ^ Mertowska P, Mertowski S, Smarz-Widelska I, Grywalska E (January 2022). "Biological Role, Mechanism of Action and the Importance of Interleukins in Kidney Diseases". International Journal of Molecular Sciences. 23 (2): 647. doi:10.3390/ijms23020647. PMC 8775480. PMID 35054831.
  9. ^ a b Catalan-Dibene J, Vazquez MI, Luu VP, Nuccio SP, Karimzadeh A, Kastenschmidt JM, et al. (November 2017). "Identification of IL-40, a Novel B Cell-Associated Cytokine". Journal of Immunology. 199 (9): 3326–3335. doi:10.4049/jimmunol.1700534. PMC 5667921. PMID 28978694.
  10. ^ Zhang C, Wei X, Omenn GS, Zhang Y (December 2018). "Structure and Protein Interaction-Based Gene Ontology Annotations Reveal Likely Functions of Uncharacterized Proteins on Human Chromosome 17". Journal of Proteome Research. 17 (12): 4186–4196. doi:10.1021/acs.jproteome.8b00453. PMC 6438760. PMID 30265558.
  11. ^ McGhee JR, Mestecky J, Elson CO, Kiyono H (May 1989). "Regulation of IgA synthesis and immune response by T cells and interleukins". Journal of Clinical Immunology. 9 (3): 175–199. doi:10.1007/BF00916814. PMID 2671008. S2CID 10344350.
  12. ^ a b c d e f Nussrat SW, Ad'hiah AH (February 2023). "Interleukin-40 is a promising biomarker associated with type 2 diabetes mellitus risk". Immunology Letters. 254: 1–5. doi:10.1016/j.imlet.2023.01.006. PMID 36640967. S2CID 255825232.
  13. ^ Hreggvidsdottir HS, Noordenbos T, Baeten DL (January 2014). "Inflammatory pathways in spondyloarthritis". Molecular Immunology. The pathogenesis of ankylosing spondylitis: HLA-B27 and beyond. 57 (1): 28–37. doi:10.1016/j.molimm.2013.07.016. PMID 23969080.
  14. ^ Sveaas SH, Berg IJ, Provan SA, Semb AG, Olsen IC, Ueland T, et al. (2015-03-04). "Circulating levels of inflammatory cytokines and cytokine receptors in patients with ankylosing spondylitis: a cross-sectional comparative study". Scandinavian Journal of Rheumatology. 44 (2): 118–124. doi:10.3109/03009742.2014.956142. PMID 25756521. S2CID 19076263.
  15. ^ Yang MG, Tian S, Zhang Q, Han J, Liu C, Zhou Y, et al. (November 2020). "Elevated serum interleukin-39 levels in patients with neuromyelitis optica spectrum disorders correlated with disease severity". Multiple Sclerosis and Related Disorders. 46: 102430. doi:10.1016/j.msard.2020.102430. PMID 32853892. S2CID 221359748.
  16. ^ Russell SE, Horan RM, Stefanska AM, Carey A, Leon G, Aguilera M, et al. (September 2016). "IL-36α expression is elevated in ulcerative colitis and promotes colonic inflammation". Mucosal Immunology. 9 (5): 1193–1204. doi:10.1038/mi.2015.134. PMID 26813344. S2CID 21305284.
  17. ^ a b c d e f g h i Navrátilová A, Andrés Cerezo L, Hulejová H, Bečvář V, Tomčík M, Komarc M, Veigl D, Tegzová D, Závada J, Olejárová M, Pavelka K, Vencovský J, Šenolt L (2021). "IL-40: A New B Cell-Associated Cytokine Up-Regulated in Rheumatoid Arthritis Decreases Following the Rituximab Therapy and Correlates With Disease Activity, Autoantibodies, and NETosis". Frontiers in Immunology. 12: 745523. doi:10.3389/fimmu.2021.745523. PMC 8566875. PMID 34745117.
  18. ^ a b c d Navrátilová A, Bečvář V, Hulejová H, Tomčík M, Štolová L, Mann H, Růžičková O, Šléglová O, Závada J, Pavelka K, Vencovský J, Šenolt L, Andrés Cerezo L (May 2023). "New pro-inflammatory cytokine IL-40 is produced by activated neutrophils and plays a role in the early stages of seropositive rheumatoid arthritis". RMD Open. 9 (2): e002894. doi:10.1136/rmdopen-2022-002894. PMC 10201233. PMID 37208028.
  19. ^ Scherer HU, Häupl T, Burmester GR (June 2020). "The etiology of rheumatoid arthritis". Journal of Autoimmunity. 110: 102400. doi:10.1016/j.jaut.2019.102400. hdl:1887/3183011. PMID 31980337.
  20. ^ a b c Jaber AS, Ad'hiah AH (February 2023). "A novel signature of interleukins 36α, 37, 38, 39 and 40 in ankylosing spondylitis". Cytokine. 162: 156117. doi:10.1016/j.cyto.2022.156117. PMID 36586188. S2CID 255298394.
  21. ^ a b c d e f g h Guggino G, Rizzo C, Mohammadnezhad L, Lo Pizzo M, Lentini VL, Di Liberto D, La Barbera L, Raimondo S, Shekarkar Azgomi M, Urzì O, Berardicurti O, Campisi G, Alessandro R, Giacomelli R, Dieli F, Ciccia F (May 2023). "Possible role for IL-40 and IL-40-producing cells in the lymphocytic infiltrated salivary glands of patients with primary Sjögren's syndrome". RMD Open. 9 (2): e002738. doi:10.1136/rmdopen-2022-002738. PMC 10163598. PMID 37137540.
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