2014
DOI: 10.1016/j.crohns.2014.02.009
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Effect of interleukin-17 on gene expression profile of fibroblasts from Crohn's disease patients

Abstract: The enhanced expression of IL-17 that is observed in patients with Crohn's disease could act on intestinal fibroblasts to induce expression of transcription factor NFKBIZ and proinflammatory chemokine CXCL1. This can have consequences for fibroblast activity and neutrophil chemotaxis.

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Cited by 28 publications
(16 citation statements)
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“…Hypertrophic scars and keloids may be a consequence of cutaneous injury as in acne and are associated with upregulation of many proinflammatory cytokines on histopathological examinations . IL‐17 was found to induce the expression of multiple inflammation‐associated genes such as IL‐8, IL‐6, intercellular adhesion molecule (ICAM)‐1, and granulocyte/macrophage‐colony stimulating factor (GM‐CSF) and to stimulate CXCL1, CXCL2, CXCL5, and CXCL8 in human epithelium.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Hypertrophic scars and keloids may be a consequence of cutaneous injury as in acne and are associated with upregulation of many proinflammatory cytokines on histopathological examinations . IL‐17 was found to induce the expression of multiple inflammation‐associated genes such as IL‐8, IL‐6, intercellular adhesion molecule (ICAM)‐1, and granulocyte/macrophage‐colony stimulating factor (GM‐CSF) and to stimulate CXCL1, CXCL2, CXCL5, and CXCL8 in human epithelium.…”
Section: Discussionmentioning
confidence: 99%
“…limited data about acne scars pathogenesis suggested us to investigate and compare the serum level of IL-17 between scarring and nonscarring acne patients. Serum IL-17 concentrations were significantly higher in scarring acne patients when compared to those without acne scars.Hypertrophic scars and keloids may be a consequence of cutaneous injury as in acne and are associated with upregulation of many proinflammatory cytokines on histopathological examinations 22. IL-17 was found to induce the expression of multiple inflammationassociated genes such as IL-8, IL-6, intercellular adhesion molecule (ICAM)-1, and granulocyte/macrophage-colony stimulating factor (GM-CSF) and to stimulate CXCL1, CXCL2, CXCL5, and CXCL8 in human epithelium.…”
mentioning
confidence: 99%
“…Although crucial in protecting the host from invasion by many types of pathogens, dysregulated IL-17A production can result in excessive proinflammatory cytokine expression and chronic inflammation, which lead to tissue damage and autoimmunity. IL-17 family cytokines have been linked to many autoimmune diseases, including multiple sclerosis (MS), rheumatoid arthritis (RA), inflammatory bowel disease, and psoriasis [6,9,15,20].…”
Section: Introductionmentioning
confidence: 99%
“…In patients with ulcerative colitis, the expression of lipocalin-2, an essential marker of activity of the disease, is regulated synergically by IL17-A, IL22 and TNFα in an IκBζ-dependent manner [ 76 , 77 ]. Likewise, an important role of IκBζ was highlighted in various autoimmune diseases, for example in Sjögren's syndrome-like disease [ 78 ], Crohn's disease [ 79 ], rhumatoid arthritis [ 80 ] as well as in psoriasis. For this last disease, a new susceptibility DNA polymorphism (rs7637230, G→A) was found at a locus adjacent to NFKBIZ [ 81 ].…”
Section: Iκbζmentioning
confidence: 99%