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Cell-cell interactions in synovitis: Interactions between T lymphocytes and synovial cells

Mechanisms whereby T lymphocytes contribute to synovial inflammation in rheumatoid arthritis are poorly understood. Here we review data that indicate an important role for cell contact between synovial T cells, adjacent macrophages and fibroblast-like synoviocytes (FLS). Thus, T cells activated by c...

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Detalles Bibliográficos
Autores principales: McInnes, Iain B, Leung, Bernard P, Liew, Foo Y
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC130139/
https://www.ncbi.nlm.nih.gov/pubmed/11094451
http://dx.doi.org/10.1186/ar115
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author McInnes, Iain B
Leung, Bernard P
Liew, Foo Y
author_facet McInnes, Iain B
Leung, Bernard P
Liew, Foo Y
author_sort McInnes, Iain B
collection PubMed
description Mechanisms whereby T lymphocytes contribute to synovial inflammation in rheumatoid arthritis are poorly understood. Here we review data that indicate an important role for cell contact between synovial T cells, adjacent macrophages and fibroblast-like synoviocytes (FLS). Thus, T cells activated by cytokines, endothelial transmigration, extracellular matrix or by auto-antigens can promote cytokine, particularly TNFα, metalloproteinase production by macrophages and FLS through cell-membrane interactions, mediated at least through β-integrins and membrane cytokines. Since soluble factors thus induced may in turn contribute directly to T cell activation, positive feedback loops are likely to be created. These novel pathways represent exciting potential therapeutic targets.
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spelling pubmed-1301392002-10-29 Cell-cell interactions in synovitis: Interactions between T lymphocytes and synovial cells McInnes, Iain B Leung, Bernard P Liew, Foo Y Arthritis Res Review Mechanisms whereby T lymphocytes contribute to synovial inflammation in rheumatoid arthritis are poorly understood. Here we review data that indicate an important role for cell contact between synovial T cells, adjacent macrophages and fibroblast-like synoviocytes (FLS). Thus, T cells activated by cytokines, endothelial transmigration, extracellular matrix or by auto-antigens can promote cytokine, particularly TNFα, metalloproteinase production by macrophages and FLS through cell-membrane interactions, mediated at least through β-integrins and membrane cytokines. Since soluble factors thus induced may in turn contribute directly to T cell activation, positive feedback loops are likely to be created. These novel pathways represent exciting potential therapeutic targets. BioMed Central 2000 2000-07-18 /pmc/articles/PMC130139/ /pubmed/11094451 http://dx.doi.org/10.1186/ar115 Text en Copyright © 2000 Current Science Ltd
spellingShingle Review
McInnes, Iain B
Leung, Bernard P
Liew, Foo Y
Cell-cell interactions in synovitis: Interactions between T lymphocytes and synovial cells
title Cell-cell interactions in synovitis: Interactions between T lymphocytes and synovial cells
title_full Cell-cell interactions in synovitis: Interactions between T lymphocytes and synovial cells
title_fullStr Cell-cell interactions in synovitis: Interactions between T lymphocytes and synovial cells
title_full_unstemmed Cell-cell interactions in synovitis: Interactions between T lymphocytes and synovial cells
title_short Cell-cell interactions in synovitis: Interactions between T lymphocytes and synovial cells
title_sort cell-cell interactions in synovitis: interactions between t lymphocytes and synovial cells
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC130139/
https://www.ncbi.nlm.nih.gov/pubmed/11094451
http://dx.doi.org/10.1186/ar115
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