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Skewed distribution of proinflammatory CD4(+)CD28(null )T cells in rheumatoid arthritis
Expanded populations of CD4(+ )T cells lacking the co-stimulatory molecule CD28 (CD4(+)CD28(null )T cells) have been reported in several inflammatory disorders. In rheumatoid arthritis, increased frequencies of CD4(+)CD28(null )T cells in peripheral blood have previously been associated with extra-a...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2212553/ https://www.ncbi.nlm.nih.gov/pubmed/17825098 http://dx.doi.org/10.1186/ar2286 |
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author | Fasth, Andreas ER Snir, Omri Johansson, Anna AT Nordmark, Birgitta Rahbar, Afsar af Klint, Erik Björkström, Niklas K Ulfgren, Ann-Kristin van Vollenhoven, Ronald F Malmström, Vivianne Trollmo, Christina |
author_facet | Fasth, Andreas ER Snir, Omri Johansson, Anna AT Nordmark, Birgitta Rahbar, Afsar af Klint, Erik Björkström, Niklas K Ulfgren, Ann-Kristin van Vollenhoven, Ronald F Malmström, Vivianne Trollmo, Christina |
author_sort | Fasth, Andreas ER |
collection | PubMed |
description | Expanded populations of CD4(+ )T cells lacking the co-stimulatory molecule CD28 (CD4(+)CD28(null )T cells) have been reported in several inflammatory disorders. In rheumatoid arthritis, increased frequencies of CD4(+)CD28(null )T cells in peripheral blood have previously been associated with extra-articular manifestations and human cytomegalovirus (HCMV) infection, but their presence in and contribution to joint manifestations is not clear. In the present article we investigated the distribution of CD4(+)CD28(null )T cells in the synovial membrane, synovial fluid and peripheral blood of RA patients, and analysed the association with erosive disease and anti-citrullinated protein antibodies. CD4(+)CD28(null )T cells were infrequent in the synovial membrane and synovial fluid, despite significant frequencies in the circulation. Strikingly, the dominant TCR-Vβ subsets of CD4(+)CD28(null )T cells in peripheral blood were often absent in synovial fluid. CD4(+)CD28(null )T cells in blood and synovial fluid showed specificity for HCMV antigens, and their presence was clearly associated with HCMV seropositivity but not with anti-citrullinated protein antibodies in the serum or synovial fluid, nor with erosive disease. Together these data imply a primary role for CD4(+)CD28(null )T cells in manifestations elsewhere than in the joints of patients with HCMV-seropositive rheumatoid arthritis. |
format | Text |
id | pubmed-2212553 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-22125532008-01-24 Skewed distribution of proinflammatory CD4(+)CD28(null )T cells in rheumatoid arthritis Fasth, Andreas ER Snir, Omri Johansson, Anna AT Nordmark, Birgitta Rahbar, Afsar af Klint, Erik Björkström, Niklas K Ulfgren, Ann-Kristin van Vollenhoven, Ronald F Malmström, Vivianne Trollmo, Christina Arthritis Res Ther Research Article Expanded populations of CD4(+ )T cells lacking the co-stimulatory molecule CD28 (CD4(+)CD28(null )T cells) have been reported in several inflammatory disorders. In rheumatoid arthritis, increased frequencies of CD4(+)CD28(null )T cells in peripheral blood have previously been associated with extra-articular manifestations and human cytomegalovirus (HCMV) infection, but their presence in and contribution to joint manifestations is not clear. In the present article we investigated the distribution of CD4(+)CD28(null )T cells in the synovial membrane, synovial fluid and peripheral blood of RA patients, and analysed the association with erosive disease and anti-citrullinated protein antibodies. CD4(+)CD28(null )T cells were infrequent in the synovial membrane and synovial fluid, despite significant frequencies in the circulation. Strikingly, the dominant TCR-Vβ subsets of CD4(+)CD28(null )T cells in peripheral blood were often absent in synovial fluid. CD4(+)CD28(null )T cells in blood and synovial fluid showed specificity for HCMV antigens, and their presence was clearly associated with HCMV seropositivity but not with anti-citrullinated protein antibodies in the serum or synovial fluid, nor with erosive disease. Together these data imply a primary role for CD4(+)CD28(null )T cells in manifestations elsewhere than in the joints of patients with HCMV-seropositive rheumatoid arthritis. BioMed Central 2007 2007-09-07 /pmc/articles/PMC2212553/ /pubmed/17825098 http://dx.doi.org/10.1186/ar2286 Text en Copyright © 2007 Fasth et al., licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Fasth, Andreas ER Snir, Omri Johansson, Anna AT Nordmark, Birgitta Rahbar, Afsar af Klint, Erik Björkström, Niklas K Ulfgren, Ann-Kristin van Vollenhoven, Ronald F Malmström, Vivianne Trollmo, Christina Skewed distribution of proinflammatory CD4(+)CD28(null )T cells in rheumatoid arthritis |
title | Skewed distribution of proinflammatory CD4(+)CD28(null )T cells in rheumatoid arthritis |
title_full | Skewed distribution of proinflammatory CD4(+)CD28(null )T cells in rheumatoid arthritis |
title_fullStr | Skewed distribution of proinflammatory CD4(+)CD28(null )T cells in rheumatoid arthritis |
title_full_unstemmed | Skewed distribution of proinflammatory CD4(+)CD28(null )T cells in rheumatoid arthritis |
title_short | Skewed distribution of proinflammatory CD4(+)CD28(null )T cells in rheumatoid arthritis |
title_sort | skewed distribution of proinflammatory cd4(+)cd28(null )t cells in rheumatoid arthritis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2212553/ https://www.ncbi.nlm.nih.gov/pubmed/17825098 http://dx.doi.org/10.1186/ar2286 |
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