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Journal articles on the topic 'IL-22'

Author: Grafiati

Published: 4 June 2021

Last updated: 26 July 2025

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1

Dempsey, Laurie A. "Antimicrobial IL-22." Nature Immunology 18, no. 4 (2017): 373. http://dx.doi.org/10.1038/ni.3722.

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2

Logiodice, Federica, Letizia Lombardelli, Ornela Kullolli, et al. "Decidual Interleukin-22-Producing CD4+ T Cells (Th17/Th0/IL-22+ and Th17/Th2/IL-22+, Th2/IL-22+, Th0/IL-22+), Which Also Produce IL-4, Are Involved in the Success of Pregnancy." International Journal of Molecular Sciences 20, no. 2 (2019): 428. http://dx.doi.org/10.3390/ijms20020428.

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Trophoblast expressing paternal HLA-C resembles a semiallograft, and could be rejected by maternal T cells. IL-22 seems to be involved in allograft rejection and thus could be responsible for miscarriages. We examined the role of decidual IL-22-producing CD4+ T on human pregnancy. In those experiencing successful pregnancy and those experiencing unexplained recurrent abortion (URA), the levels of IL-22 produced by decidual CD4+ T cells are higher than those of peripheral blood T cells. We found a correlation of IL-22 and IL-4 produced by decidual CD4+ T cells in those experiencing successful p

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3

Tohyama, Mikiko, Yasushi Hanakawa, Yuji Shirakata, et al. "IL-17 and IL-22 mediate IL-20 subfamily cytokine production in cultured keratinocytesviaincreased IL-22 receptor expression." European Journal of Immunology 39, no. 10 (2009): 2779–88. http://dx.doi.org/10.1002/eji.200939473.

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4

Kugelberg, Elisabeth. "IL-22 complements protection." Nature Reviews Immunology 14, no. 12 (2014): 781. http://dx.doi.org/10.1038/nri3768.

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5

Conti, P., D. Kempuraj, S. Frydas, et al. "IL-10 subfamily members: IL-19, IL-20, IL-22, IL-24 and IL-26." Immunology Letters 88, no. 3 (2003): 171–74. http://dx.doi.org/10.1016/s0165-2478(03)00087-7.

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6

Orlandini, Giovanni. "Il distacco transnazionale dopo il d.lgs. 22/2020." GIORNALE DI DIRITTO DEL LAVORO E DI RELAZIONI INDUSTRIALI, no. 168 (January 2021): 749–65. http://dx.doi.org/10.3280/gdl2020-168005.

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. L'articolo analizza le principali questioni giuridiche che rendono problematica l'applicazione della disciplina del distacco transnazionale nell'ordinamento italiano, contribuendo ad esporlo al dumping operato da imprese con sede in altri Stati. L'analisi si sofferma in particolare sulle novità introdotte dal d.lgs. n. 22 del 15 settembre 2020 che ha riformato il d.lgs. 136/16 rece-pendo la direttiva 2018/957. Il regime protettivo del lavoratore straniero distaccato in Italia, pur uscendo rafforzato dalla novella, continua a scontare gli effetti di un sistema di contrattazione collettiva pat

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7

Eyerich, Stefanie, Kilian Eyerich, Andrea Cavani, and Carsten Schmidt-Weber. "IL-17 and IL-22: siblings, not twins." Trends in Immunology 31, no. 9 (2010): 354–61. http://dx.doi.org/10.1016/j.it.2010.06.004.

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8

Lim, Chrissie, MeeAe Hong, and Ram Savan. "The human IL-22 binding protein isoforms are a rheostat for IL-22 signaling." Journal of Immunology 196, no. 1_Supplement (2016): 189.6. http://dx.doi.org/10.4049/jimmunol.196.supp.189.6.

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Abstract The cytokine interleukin-22 (IL-22) activates signal transducer and activator of transcription 3 (STAT3) to drive various processes central to tissue homeostasis and immunosurveillance; its dysregulation causes inflammatory diseases. IL-22 has a soluble receptor, IL-22 binding protein (IL-22BP; IL22RA2), which antagonizes IL-22 activity and has genetic associations with autoimmune diseases. Humans express three IL-22BP isoforms, whereas mice only express an IL-22BPi2 homolog. Given the lack of IL-22BPi1 and IL-22BPi3 expression in mice, there has not been a thorough characterization o

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9

Crunkhorn, Sarah. "IL-22 blockade alleviates anaemia." Nature Reviews Drug Discovery 20, no. 5 (2021): 344. http://dx.doi.org/10.1038/d41573-021-00059-x.

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10

Bird, Lucy. "Antimicrobial function for IL-22." Nature Reviews Microbiology 6, no. 4 (2008): 259. http://dx.doi.org/10.1038/nrmicro1884.

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11

Williams, Ifor. "Drivers of IL-22 secretion." Science 368, no. 6490 (2020): 484.18–486. http://dx.doi.org/10.1126/science.368.6490.484-r.

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12

Laska, Julia, Maciej Tota, Julia Łacwik, Łukasz Sędek, and Krzysztof Gomułka. "IL-22 in Atopic Dermatitis." Cells 13, no. 16 (2024): 1398. http://dx.doi.org/10.3390/cells13161398.

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Atopic dermatitis (AD) is a prevalent and chronic inflammatory skin condition characterized by a multifaceted pathophysiology that gives rise to diverse clinical manifestations. The management of AD remains challenging due to the suboptimal efficacy of existing treatment options. Nonetheless, recent progress in elucidating the underlying mechanisms of the disease has facilitated the identification of new potential therapeutic targets and promising drug candidates. In this review, we summarize the newest data, considering multiple connections between IL-22 and AD. The presence of circulating IL

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13

Sargent, Jennifer. "IL-22 and metabolic disease." Nature Reviews Endocrinology 10, no. 11 (2014): 639. http://dx.doi.org/10.1038/nrendo.2014.148.

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14

Mueller, K. L. "IL-22 Protects the Thymus." Science Signaling 5, no. 219 (2012): ec107-ec107. http://dx.doi.org/10.1126/scisignal.2003115.

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15

Thoma, Clemens. "IL-22 assures gut homeostasis." Nature Reviews Gastroenterology & Hepatology 16, no. 4 (2019): 199. http://dx.doi.org/10.1038/s41575-019-0124-z.

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16

Fehervari, Zoltan. "IL-22 controls transmissible colitis." Nature Immunology 14, no. 7 (2013): 691. http://dx.doi.org/10.1038/ni.2657.

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17

Dempsey, Laurie A. "IL-22 in Peyer's patches." Nature Immunology 18, no. 7 (2017): 715. http://dx.doi.org/10.1038/ni.3786.

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18

Ouyang, W., and P. Valdez. "IL-22 in mucosal immunity." Mucosal Immunology 1, no. 5 (2008): 335–38. http://dx.doi.org/10.1038/mi.2008.26.

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19

Rittenhouse, Peter A. "IL-22's gut feeling." Science-Business eXchange 1, no. 7 (2008): 155. http://dx.doi.org/10.1038/scibx.2008.155.

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20

Kugelberg, Elisabeth. "IL-22 controls iron scavenging." Nature Reviews Immunology 17, no. 3 (2017): 146–47. http://dx.doi.org/10.1038/nri.2017.15.

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21

Bird, Lucy. "Antimicrobial function for IL-22." Nature Reviews Immunology 8, no. 3 (2008): 163. http://dx.doi.org/10.1038/nri2290.

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22

Zelante, Teresa, Rossana Iannitti, Antonella De Luca, and Luigina Romani. "IL-22 in antifungal immunity." European Journal of Immunology 41, no. 2 (2011): 270–75. http://dx.doi.org/10.1002/eji.201041246.

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23

Lim, Chrissie, MeeAe Hong, and Ram Savan. "Human IL-22 binding protein isoforms act as a rheostat for IL-22 signaling." Science Signaling 9, no. 447 (2016): ra95. http://dx.doi.org/10.1126/scisignal.aad9887.

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24

Fotiadou, Christina, Elizabeth Lazaridou, Eleni Sotiriou, et al. "IL-17A, IL-22, and IL-23 as Markers of Psoriasis Activity." Journal of Cutaneous Medicine and Surgery 19, no. 6 (2015): 555–60. http://dx.doi.org/10.1177/1203475415584503.

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Introduction: T-helper 1 (Th1), Th17 cells, and their related cytokines are implicated in psoriasis pathogenesis although the contribution of each group of cytokines in psoriasis activity has not been fully clarified. Objectives: To investigate whether Th17-related cytokines are associated with psoriasis activity. Methods: The serum levels of interleukin (IL)-1β, 6, 8, 17Α, 22, 23, and tumor necrosis factor-α (TNFα) were measured with flow cytometry in 35 patients with plaque psoriasis (21 with stable and 14 with active disease) and in 20 healthy controls. Results: Interleukin-6, 8, 17A, 22, 2

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25

Bleicher, Lucas, Patricia Ribeiro de Moura, Leandra Watanabe, et al. "Crystal structure of the IL-22/IL-22R1 complex and its implications for the IL-22 signaling mechanism." FEBS Letters 582, no. 20 (2008): 2985–92. http://dx.doi.org/10.1016/j.febslet.2008.07.046.

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26

Amini, Behbahani A., M. Sattari, R. Mofid, and A. Ganji. "Interleukin-22 (IL-22) Gingival Gene Expression and GCF Concentration in Periodontal Health and Disease." International Journal of Dentistry and Oral Science (IJDOS) 1, no. 2 (2014): 21–25. https://doi.org/10.19070/2377-8075-140005.

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IL-22 is a cytokine that is assumed to improve anti-microbial defense of epidermal and epithelial cells and the cells of gastrointestinal and respiratory systems. With respect to absence of enough relevant articles in this regard the aim of this study was to evaluate the correlation between IL-22 gene expression in gingival tissues as well as its concentration in GCF and periodontal diseases. Gingival samples obtained from 60 patients of three different groups (healthy, gingivitis and chronic periodontitis) and used for evaluation. Expression of IL-22 mRNA was measured by R

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27

Eyerich, S., C. Traidl-Hoffmann, H. Behrendt, et al. "Neue Schlüsselzytokine in der Allergologie: IL-17, IL-22." Allergologie 34, no. 07 (2011): 344–49. http://dx.doi.org/10.5414/alp34344.

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28

Eyerich, S., C. Traidl-Hoffmann, H. Behrendt, et al. "Novel key cytokines in allergy: IL-17, IL-22." Allergologie select 1, no. 1 (2017): 71–76. http://dx.doi.org/10.5414/alx01403e.

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29

Sabat, Robert, Wenjun Ouyang, and Kerstin Wolk. "Therapeutic opportunities of the IL-22–IL-22R1 system." Nature Reviews Drug Discovery 13, no. 1 (2013): 21–38. http://dx.doi.org/10.1038/nrd4176.

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30

Souwer, Yuri, Krisztina Szegedi, Martien L. Kapsenberg, and Esther C. de Jong. "IL-17 and IL-22 in atopic allergic disease." Current Opinion in Immunology 22, no. 6 (2010): 821–26. http://dx.doi.org/10.1016/j.coi.2010.10.013.

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31

Giannou, Anastasios D., Jöran Lücke, Dörte Kleinschmidt, et al. "A Critical Role of the IL-22–IL-22 Binding Protein Axis in Hepatocellular Carcinoma." Cancers 14, no. 24 (2022): 6019. http://dx.doi.org/10.3390/cancers14246019.

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Hepatocellular carcinoma (HCC) ranks among the five most common cancer entities worldwide and leads to hundred-thousands of deaths every year. Despite some groundbreaking therapeutical revelations during the last years, the overall prognosis remains poor. Although the immune system fights malignant transformations with a robust anti-tumor response, certain immune mediators have also been shown to promote cancer development. For example, interleukin (IL)-22 has been associated with HCC progression and worsened prognosis in multiple studies. However, the underlying mechanisms of the pathological

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32

Hakemi, MazdakGanjalikhani, Nahid Eskandari, Reza Yazdani, Rahim Farahani, and Roya Sherkat. "Cytokines (interleukin-9, IL-17, IL-22, IL-25 and IL-33) and asthma." Advanced Biomedical Research 3, no. 1 (2014): 127. http://dx.doi.org/10.4103/2277-9175.133249.

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33

Moniaga, Catharina Sagita, Gyohei Egawa, Yoshiki Miyachi, and Kenji Kabashima. "Calcipotriol modulates IL-22 receptor expression and keratinocyte proliferation in IL-22-induced epidermal hyperplasia." Journal of Dermatological Science 71, no. 1 (2013): 76–77. http://dx.doi.org/10.1016/j.jdermsci.2013.03.011.

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34

Hu, Yehfang, Yamila Carpio, Callum Scott, et al. "Induction of IL-22 protein and IL-22-producing cells in rainbow trout Oncorhynchus mykiss." Developmental & Comparative Immunology 101 (December 2019): 103449. http://dx.doi.org/10.1016/j.dci.2019.103449.

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35

Guo, Hailong, and David J. Topham. "Interleukin-22 (IL-22) Production by Pulmonary Natural Killer Cells and the Potential Role of IL-22 during Primary Influenza Virus Infection." Journal of Virology 84, no. 15 (2010): 7750–59. http://dx.doi.org/10.1128/jvi.00187-10.

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ABSTRACT We set out to test the hypothesis that interleukin-22 (IL-22), a cytokine crucial for epithelial cell homeostasis and recovery from tissue injury, would be protective during influenza virus infection. Recent studies have identified phenotypically and functionally unique intestinal NK cells capable of producing the cytokine IL-22. Unlike gut NK cells that produce IL-22, the surface phenotypes of lung NK cells were similar to those of spleen NK cells and were characteristically mature. With mitogen stimulation, both single and double IL-22- and gamma interferon (IFN-γ)-producing lung NK

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36

Commins, Scott, John W. Steinke, and Larry Borish. "The extended IL-10 superfamily: IL-10, IL-19, IL-20, IL-22, IL-24, IL-26, IL-28, and IL-29." Journal of Allergy and Clinical Immunology 121, no. 5 (2008): 1108–11. http://dx.doi.org/10.1016/j.jaci.2008.02.026.

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37

Chen, Feidi. "mTOR mediates IL-23 induction of neutrophil IL-17 and IL-22 production (MUC5P.745)." Journal of Immunology 194, no. 1_Supplement (2015): 138.3. http://dx.doi.org/10.4049/jimmunol.194.supp.138.3.

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Abstract It has been shown recently that neutrophils are able to produce IL-22 and IL-17, which differentially regulate the pathogenesis of inflammatory bowel disease. However, it is still largely unknown how the neutrophil production of IL-22 and IL-17 is regulated, and what the receptors are required. We demonstrated that, in a microbiota antigen specific T-cell mediated colitis model, neutrophils accumulated in the intestines prior to intestinal inflammation. Depletion of neutrophils resulted in a significant increase of colitis development, indicating a protective role of neutrophils in co

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38

Huo, Hui Jun, Shan Nan Chen, Li Li, Zubair Ahmed Laghari, Nan Li, and Pin Nie. "Functional characterization of interleukin (IL)-22 and its inhibitor, IL-22 binding protein (IL-22BP) in Mandarin fish, Siniperca chuatsi." Developmental & Comparative Immunology 97 (August 2019): 88–97. http://dx.doi.org/10.1016/j.dci.2019.03.007.

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39

Sertorio, Mathieu, Xunya Hou, Rodrigo F. Carmo, et al. "IL-22 and IL-22 binding protein (IL-22BP) regulate fibrosis and cirrhosis in hepatitis C virus and schistosome infections." Hepatology 61, no. 4 (2015): 1321–31. http://dx.doi.org/10.1002/hep.27629.

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40

Zhang, Jing-Ru, Dan-Dan Pang, Qiang Tong, Xia Liu, Ding-Feng Su, and Sheng-Ming Dai. "Different Modulatory Effects of IL-17, IL-22, and IL-23 on Osteoblast Differentiation." Mediators of Inflammation 2017 (2017): 1–11. http://dx.doi.org/10.1155/2017/5950395.

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Objectives. To examine the expressions of IL-17, IL-22, and IL-23 receptors in four osteoblast models and the effects of IL-17, IL-22, and IL-23 on osteoblasts.Methods. Gene expression levels of receptors, alkaline phosphatase (ALP), osteocalcin (OCN), and Runt-related transcription factor 2 (Runx-2), were evaluated by RT-PCR and real-time RT-PCR. Proliferative responses and cell cycle analysis were detected by a CCK-8 assay and flow cytometry, respectively. ALP activity and ALP mass were detected by an ALP activity assay and ALP staining, respectively.Results. In primary osteoblasts, only the

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41

Kotenko, Sergei V., Lara S. Izotova, Olga V. Mirochnitchenko, et al. "Identification of the Functional Interleukin-22 (IL-22) Receptor Complex." Journal of Biological Chemistry 276, no. 4 (2000): 2725–32. http://dx.doi.org/10.1074/jbc.m007837200.

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42

Mühl, Heiko, and Malte Bachmann. "IL-18/IL-18BP and IL-22/IL-22BP: Two interrelated couples with therapeutic potential." Cellular Signalling 63 (November 2019): 109388. http://dx.doi.org/10.1016/j.cellsig.2019.109388.

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43

Sabihi, Morsal, Marius Böttcher, Penelope Pelczar, and Samuel Huber. "Microbiota-Dependent Effects of IL-22." Cells 9, no. 10 (2020): 2205. http://dx.doi.org/10.3390/cells9102205.

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Cytokines are important contributors to immune responses against microbial and environmental threats and are of particular importance at epithelial barriers. These interfaces are continuously exposed to external factors and thus require immune components to both protect the host from pathogen invasion and to regulate overt inflammation. Recently, substantial efforts have been devoted to understanding how cytokines act on certain cells at barrier sites, and why the dysregulation of immune responses may lead to pathogenesis. In particular, the cytokine IL-22 is involved in preserving an intact e

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44

Mühl, Heiko, Patrick Scheiermann, Malte Bachmann, Lorena Härdle, Anika Heinrichs, and Josef Pfeilschifter. "IL-22 in tissue-protective therapy." British Journal of Pharmacology 169, no. 4 (2013): 761–71. http://dx.doi.org/10.1111/bph.12196.

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45

Harrison, Charlotte. "IL-22: linking inflammation and cancer." Nature Reviews Drug Discovery 12, no. 7 (2013): 505. http://dx.doi.org/10.1038/nrd4065.

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46

Zenewicz, L. A., and R. A. Flavell. "Recent advances in IL-22 biology." International Immunology 23, no. 3 (2011): 159–63. http://dx.doi.org/10.1093/intimm/dxr001.

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47

Datta, Sandip K. "IL-22: Scavenging beyond the barrier." Science Immunology 2, no. 8 (2017): eaam7039. http://dx.doi.org/10.1126/sciimmunol.aam7039.

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48

Lu, Zhou, Ronghua Liu, Enyu Huang, and Yiwei Chu. "MicroRNAs: New regulators of IL-22." Cellular Immunology 304-305 (June 2016): 1–8. http://dx.doi.org/10.1016/j.cellimm.2016.05.003.

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49

Nikoopour, Enayat, Stacey M. Bellemore, and Bhagirath Singh. "IL-22, cell regeneration and autoimmunity." Cytokine 74, no. 1 (2015): 35–42. http://dx.doi.org/10.1016/j.cyto.2014.09.007.

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50

Bernink, Jochem H. "The sweet side of IL-22." Nature Microbiology 10, no. 3 (2025): 610–12. https://doi.org/10.1038/s41564-025-01945-5.

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