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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...

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Autores principales: 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
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
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.
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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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