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Spleen tyrosine kinase inhibition in the treatment of autoimmune, allergic and autoinflammatory diseases

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...

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Detalles Bibliográficos
Autores principales: Pamuk, Omer N, Tsokos, George C
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3046528/
https://www.ncbi.nlm.nih.gov/pubmed/21211067
http://dx.doi.org/10.1186/ar3198
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author Pamuk, Omer N
Tsokos, George C
author_facet Pamuk, Omer N
Tsokos, George C
author_sort Pamuk, Omer N
collection PubMed
description 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.
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spelling pubmed-30465282011-06-17 Spleen tyrosine kinase inhibition in the treatment of autoimmune, allergic and autoinflammatory diseases Pamuk, Omer N Tsokos, George C Arthritis Res Ther Review 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. BioMed Central 2010 2010-12-17 /pmc/articles/PMC3046528/ /pubmed/21211067 http://dx.doi.org/10.1186/ar3198 Text en Copyright ©2010 BioMed Central Ltd
spellingShingle Review
Pamuk, Omer N
Tsokos, George C
Spleen tyrosine kinase inhibition in the treatment of autoimmune, allergic and autoinflammatory diseases
title Spleen tyrosine kinase inhibition in the treatment of autoimmune, allergic and autoinflammatory diseases
title_full Spleen tyrosine kinase inhibition in the treatment of autoimmune, allergic and autoinflammatory diseases
title_fullStr Spleen tyrosine kinase inhibition in the treatment of autoimmune, allergic and autoinflammatory diseases
title_full_unstemmed Spleen tyrosine kinase inhibition in the treatment of autoimmune, allergic and autoinflammatory diseases
title_short Spleen tyrosine kinase inhibition in the treatment of autoimmune, allergic and autoinflammatory diseases
title_sort spleen tyrosine kinase inhibition in the treatment of autoimmune, allergic and autoinflammatory diseases
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3046528/
https://www.ncbi.nlm.nih.gov/pubmed/21211067
http://dx.doi.org/10.1186/ar3198
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