Spleen tyrosine kinase inhibition in the treatment of autoimmune, allergic and autoinflammatory diseases
dc.authorwosid | tsokos, george C/O-3360-2013 | |
dc.contributor.author | Pamuk, Omer N. | |
dc.contributor.author | Tsokos, George C. | |
dc.date.accessioned | 2024-06-12T11:19:47Z | |
dc.date.available | 2024-06-12T11:19:47Z | |
dc.date.issued | 2010 | |
dc.department | Trakya Üniversitesi | en_US |
dc.description.abstract | Spleen tyrosine kinase (Syk) is involved in the development of the adaptive immune system and has been recognized as being important in the function of additional cell types, including platelets, phagocytes, fibroblasts, and osteoclasts, and in the generation of the inflammasome. Preclinical studies presented compelling evidence that Syk inhibition may have therapeutic value in the treatment of rheumatoid arthritis and other forms of arthritis, systemic lupus erythematosus, autoimmune cytopenias, and allergic and autoinflammatory diseases. In addition, Syk inhibition may have a place in limiting tissue injury associated with organ transplant and revascularization procedures. Clinical trials have documented exciting success in the treatment of patients with rheumatoid arthritis, autoimmune cytopenias, and allergic rhinitis. While the extent and severity of side effects appear to be limited so far, larger studies will unravel the risk involved with the clinical benefit. | en_US |
dc.description.sponsorship | GCT lab [PHS R01 AI42269]; DoD [W81XWH-09-1-0530]; Rigel Pharmaceuticals (South San Francisco, CA, USA); Scientific and Technological Research Council of Turkey (TUBITAK) | en_US |
dc.description.sponsorship | Work in the GCT lab was supported by PHS R01 AI42269, DoD W81XWH-09-1-0530, and a grant from Rigel Pharmaceuticals (South San Francisco, CA, USA). ONP was supported by a Scientific and Technological Research Council of Turkey (TUBITAK) scholarship. | en_US |
dc.identifier.doi | 10.1186/ar3198 | |
dc.identifier.issn | 1478-6354 | |
dc.identifier.issn | 1478-6362 | |
dc.identifier.issue | 6 | en_US |
dc.identifier.pmid | 21211067 | en_US |
dc.identifier.scopus | 2-s2.0-79959261430 | en_US |
dc.identifier.scopusquality | Q1 | en_US |
dc.identifier.uri | https://doi.org/10.1186/ar3198 | |
dc.identifier.uri | https://hdl.handle.net/20.500.14551/25340 | |
dc.identifier.volume | 12 | en_US |
dc.identifier.wos | WOS:000287517000006 | en_US |
dc.identifier.wosquality | Q2 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | en | en_US |
dc.publisher | Bmc | en_US |
dc.relation.ispartof | Arthritis Research & Therapy | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Receptor Gamma-Chain | en_US |
dc.subject | B-Cell Development | en_US |
dc.subject | Syk-Kinase | en_US |
dc.subject | Rheumatoid-Arthritis | en_US |
dc.subject | Activation | en_US |
dc.subject | Inflammation | en_US |
dc.subject | Phagocytosis | en_US |
dc.subject | Challenge | en_US |
dc.subject | Mechanism | en_US |
dc.subject | Symptoms | en_US |
dc.title | Spleen tyrosine kinase inhibition in the treatment of autoimmune, allergic and autoinflammatory diseases | en_US |
dc.type | Review Article | en_US |