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Developments in the synovial biology field 2006

Synovial pathophysiology is a complex and synergistic interplay of different cell populations with tissue components, mediated by a variety of signaling mechanisms. All of these mechanisms drive the affected joint into inflammation and drive the subsequent destruction of cartilage and bone. Each cel...

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Detalles Bibliográficos
Autores principales: Knedla, Anette, Neumann, Elena, Müller-Ladner, Ulf
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1906804/
https://www.ncbi.nlm.nih.gov/pubmed/17442097
http://dx.doi.org/10.1186/ar2140
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author Knedla, Anette
Neumann, Elena
Müller-Ladner, Ulf
author_facet Knedla, Anette
Neumann, Elena
Müller-Ladner, Ulf
author_sort Knedla, Anette
collection PubMed
description Synovial pathophysiology is a complex and synergistic interplay of different cell populations with tissue components, mediated by a variety of signaling mechanisms. All of these mechanisms drive the affected joint into inflammation and drive the subsequent destruction of cartilage and bone. Each cell type contributes significantly to the initiation and perpetuation of this deleterious concert, especially in rheumatoid arthritis. Rheumatoid arthritis synovial fibroblasts and macrophages, both cell types with pivotal roles in inflammation and destruction, but also T cells and B cells are crucial for complex network in the inflamed synovium. An even more complex cellular crosstalk between these key players maintains a process of chronic inflammation. As outlined in the present review, in the past year substantial progress has been made to elucidate further details of the rich pathophysiology of rheumatoid arthritis, which may also facilitate the identification of novel targets for future therapeutic strategies.
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spelling pubmed-19068042007-07-04 Developments in the synovial biology field 2006 Knedla, Anette Neumann, Elena Müller-Ladner, Ulf Arthritis Res Ther Review Synovial pathophysiology is a complex and synergistic interplay of different cell populations with tissue components, mediated by a variety of signaling mechanisms. All of these mechanisms drive the affected joint into inflammation and drive the subsequent destruction of cartilage and bone. Each cell type contributes significantly to the initiation and perpetuation of this deleterious concert, especially in rheumatoid arthritis. Rheumatoid arthritis synovial fibroblasts and macrophages, both cell types with pivotal roles in inflammation and destruction, but also T cells and B cells are crucial for complex network in the inflamed synovium. An even more complex cellular crosstalk between these key players maintains a process of chronic inflammation. As outlined in the present review, in the past year substantial progress has been made to elucidate further details of the rich pathophysiology of rheumatoid arthritis, which may also facilitate the identification of novel targets for future therapeutic strategies. BioMed Central 2007 2007-04-10 /pmc/articles/PMC1906804/ /pubmed/17442097 http://dx.doi.org/10.1186/ar2140 Text en Copyright © 2007 BioMed Central Ltd
spellingShingle Review
Knedla, Anette
Neumann, Elena
Müller-Ladner, Ulf
Developments in the synovial biology field 2006
title Developments in the synovial biology field 2006
title_full Developments in the synovial biology field 2006
title_fullStr Developments in the synovial biology field 2006
title_full_unstemmed Developments in the synovial biology field 2006
title_short Developments in the synovial biology field 2006
title_sort developments in the synovial biology field 2006
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1906804/
https://www.ncbi.nlm.nih.gov/pubmed/17442097
http://dx.doi.org/10.1186/ar2140
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