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An association between the acute phase response and patterns of antigen induced T cell proliferation in juvenile idiopathic arthritis

The aim of this research was to determine whether all memory T cells have the same propensity to migrate to the joint in patients with juvenile idiopathic arthritis. Paired synovial fluid and peripheral blood mononuclear cell proliferative responses to a panel of antigens were measured and the resul...

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Autores principales: Black, Antony PB, Bhayani, Hansha, Ryder, Clive AJ, Pugh, Mark T, Gardner-Medwin, Janet MM, Southwood, Taunton R
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC193728/
https://www.ncbi.nlm.nih.gov/pubmed/12932291
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author Black, Antony PB
Bhayani, Hansha
Ryder, Clive AJ
Pugh, Mark T
Gardner-Medwin, Janet MM
Southwood, Taunton R
author_facet Black, Antony PB
Bhayani, Hansha
Ryder, Clive AJ
Pugh, Mark T
Gardner-Medwin, Janet MM
Southwood, Taunton R
author_sort Black, Antony PB
collection PubMed
description The aim of this research was to determine whether all memory T cells have the same propensity to migrate to the joint in patients with juvenile idiopathic arthritis. Paired synovial fluid and peripheral blood mononuclear cell proliferative responses to a panel of antigens were measured and the results correlated with a detailed set of laboratory and clinical data from 39 patients with juvenile idiopathic arthritis. Two distinct patterns of proliferative response were found in the majority of patients: a diverse pattern, in which synovial fluid responses were greater than peripheral blood responses for all antigens tested; and a restricted pattern, in which peripheral blood responses to some antigens were more vigorous than those in the synovial fluid compartment. The diverse pattern was generally found in patients with a high acute phase response, whereas patients without elevated acute phase proteins were more likely to demonstrate a restricted pattern. We propose that an association between the synovial fluid T cell repertoire and the acute phase response suggests that proinflammatory cytokines may influence recruitment of memory T cells to an inflammatory site, independent of their antigen specificity. Additionally, increased responses to enteric bacteria and the presence of αEβ7 T cells in synovial fluid may reflect accumulation of gut associated T cells in the synovial compartment, even in the absence of an elevated acute phase response. This is the first report of an association between the acute phase response and the T cell population recruited to an inflammatory site.
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spelling pubmed-1937282003-09-15 An association between the acute phase response and patterns of antigen induced T cell proliferation in juvenile idiopathic arthritis Black, Antony PB Bhayani, Hansha Ryder, Clive AJ Pugh, Mark T Gardner-Medwin, Janet MM Southwood, Taunton R Arthritis Res Ther Research Article The aim of this research was to determine whether all memory T cells have the same propensity to migrate to the joint in patients with juvenile idiopathic arthritis. Paired synovial fluid and peripheral blood mononuclear cell proliferative responses to a panel of antigens were measured and the results correlated with a detailed set of laboratory and clinical data from 39 patients with juvenile idiopathic arthritis. Two distinct patterns of proliferative response were found in the majority of patients: a diverse pattern, in which synovial fluid responses were greater than peripheral blood responses for all antigens tested; and a restricted pattern, in which peripheral blood responses to some antigens were more vigorous than those in the synovial fluid compartment. The diverse pattern was generally found in patients with a high acute phase response, whereas patients without elevated acute phase proteins were more likely to demonstrate a restricted pattern. We propose that an association between the synovial fluid T cell repertoire and the acute phase response suggests that proinflammatory cytokines may influence recruitment of memory T cells to an inflammatory site, independent of their antigen specificity. Additionally, increased responses to enteric bacteria and the presence of αEβ7 T cells in synovial fluid may reflect accumulation of gut associated T cells in the synovial compartment, even in the absence of an elevated acute phase response. This is the first report of an association between the acute phase response and the T cell population recruited to an inflammatory site. BioMed Central 2003 2003-07-07 /pmc/articles/PMC193728/ /pubmed/12932291 Text en Copyright © 2003 Black et al., licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Research Article
Black, Antony PB
Bhayani, Hansha
Ryder, Clive AJ
Pugh, Mark T
Gardner-Medwin, Janet MM
Southwood, Taunton R
An association between the acute phase response and patterns of antigen induced T cell proliferation in juvenile idiopathic arthritis
title An association between the acute phase response and patterns of antigen induced T cell proliferation in juvenile idiopathic arthritis
title_full An association between the acute phase response and patterns of antigen induced T cell proliferation in juvenile idiopathic arthritis
title_fullStr An association between the acute phase response and patterns of antigen induced T cell proliferation in juvenile idiopathic arthritis
title_full_unstemmed An association between the acute phase response and patterns of antigen induced T cell proliferation in juvenile idiopathic arthritis
title_short An association between the acute phase response and patterns of antigen induced T cell proliferation in juvenile idiopathic arthritis
title_sort association between the acute phase response and patterns of antigen induced t cell proliferation in juvenile idiopathic arthritis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC193728/
https://www.ncbi.nlm.nih.gov/pubmed/12932291
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