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Ustekinumab in Psoriasis Immunopathology with Emphasis on the Th17-IL23 Axis: A Primer
Psoriasis is a chronic relapsing immunoinflammatory dermatosis that is commonly associated with systemic comorbidities. The pathogenic importance of interleukin (IL)-12 and IL-23 is beyond doubt, as well as the involvement of T helper cells (Th)1 and Th17 cells. There is upregulation of the p40 subu...
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Published in: | BioMed research international 2012-01, Vol.2012 (2012), p.1-5 |
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description | Psoriasis is a chronic relapsing immunoinflammatory dermatosis that is commonly associated with systemic comorbidities. The pathogenic importance of interleukin (IL)-12 and IL-23 is beyond doubt, as well as the involvement of T helper cells (Th)1 and Th17 cells. There is upregulation of the p40 subunit shared by IL-12 and IL-23 and of the IL-23 p19 subunit, but not an increased expression of the IL-12 p35 subunit. This indicates that IL-23 appears more involved than IL-12 in the pathogenesis of psoriatic plaques. Ustekinumab is a fully human monoclonal antibody of the immunoglobulin (Ig) G1 class targeting the p40 subunit common to both IL-12 and IL-23, thus inhibiting both IL-12 and IL-23 receptor-mediated signalling. Ustekinumab is part of the recent biologic therapies active in psoriasis, autoimmune arthritides, and inflammatory bowel diseases. |
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The pathogenic importance of interleukin (IL)-12 and IL-23 is beyond doubt, as well as the involvement of T helper cells (Th)1 and Th17 cells. There is upregulation of the p40 subunit shared by IL-12 and IL-23 and of the IL-23 p19 subunit, but not an increased expression of the IL-12 p35 subunit. This indicates that IL-23 appears more involved than IL-12 in the pathogenesis of psoriatic plaques. Ustekinumab is a fully human monoclonal antibody of the immunoglobulin (Ig) G1 class targeting the p40 subunit common to both IL-12 and IL-23, thus inhibiting both IL-12 and IL-23 receptor-mediated signalling. Ustekinumab is part of the recent biologic therapies active in psoriasis, autoimmune arthritides, and inflammatory bowel diseases.</description><identifier>ISSN: 2314-6133</identifier><identifier>ISSN: 1110-7243</identifier><identifier>ISSN: 1110-7251</identifier><identifier>EISSN: 2314-6141</identifier><identifier>EISSN: 1110-7251</identifier><identifier>DOI: 10.1155/2012/147413</identifier><identifier>PMID: 22754278</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Antibodies, Monoclonal - therapeutic use ; Antibodies, Monoclonal, Humanized ; Cytokines ; Dermatologie ; Dermatology ; Disease ; Helper cells ; Hospitals ; Human health sciences ; Humans ; Immune system ; Interleukin-12 - immunology ; Interleukin-23 - immunology ; Pathogenesis ; Psoriasis ; Psoriasis - drug therapy ; Psoriasis - immunology ; Review ; Sciences de la santé humaine ; Skin diseases ; Th17 Cells - immunology ; Ustekinumab</subject><ispartof>BioMed research international, 2012-01, Vol.2012 (2012), p.1-5</ispartof><rights>Copyright © 2012 Pascale Quatresooz et al.</rights><rights>Copyright © 2012 Pascale Quatresooz et al. 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This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright © 2012 Pascale Quatresooz et al. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c544t-95d5b6a4229d4ce6ecc62352e9147a7671b00143fe6d65c85b3d42a6826cadd53</citedby><cites>FETCH-LOGICAL-c544t-95d5b6a4229d4ce6ecc62352e9147a7671b00143fe6d65c85b3d42a6826cadd53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1038409032/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1038409032?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22754278$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Berardesca, Enzo</contributor><creatorcontrib>Delvenne, Philippe</creatorcontrib><creatorcontrib>Humbert, Philippe</creatorcontrib><creatorcontrib>Piérard, Gérald E.</creatorcontrib><creatorcontrib>Hermanns-Lê, Trinh</creatorcontrib><creatorcontrib>Quatresooz, Pascale</creatorcontrib><creatorcontrib>Piérard-Franchimont, Claudine</creatorcontrib><title>Ustekinumab in Psoriasis Immunopathology with Emphasis on the Th17-IL23 Axis: A Primer</title><title>BioMed research international</title><addtitle>J Biomed Biotechnol</addtitle><description>Psoriasis is a chronic relapsing immunoinflammatory dermatosis that is commonly associated with systemic comorbidities. 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subjects | Antibodies, Monoclonal - therapeutic use Antibodies, Monoclonal, Humanized Cytokines Dermatologie Dermatology Disease Helper cells Hospitals Human health sciences Humans Immune system Interleukin-12 - immunology Interleukin-23 - immunology Pathogenesis Psoriasis Psoriasis - drug therapy Psoriasis - immunology Review Sciences de la santé humaine Skin diseases Th17 Cells - immunology Ustekinumab |
title | Ustekinumab in Psoriasis Immunopathology with Emphasis on the Th17-IL23 Axis: A Primer |
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