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T cells in rheumatoid arthritis

Over the past decade and a half, advances in our understanding of the pathogenesis of immune-mediated diseases such as rheumatoid arthritis (RA) have translated directly into benefit for patients. Much of this benefit has arisen through the introduction of targeted biological therapies. At the same...

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Detalles Bibliográficos
Autor principal: Cope, Andrew P
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2582813/
https://www.ncbi.nlm.nih.gov/pubmed/19007421
http://dx.doi.org/10.1186/ar2412
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author Cope, Andrew P
author_facet Cope, Andrew P
author_sort Cope, Andrew P
collection PubMed
description Over the past decade and a half, advances in our understanding of the pathogenesis of immune-mediated diseases such as rheumatoid arthritis (RA) have translated directly into benefit for patients. Much of this benefit has arisen through the introduction of targeted biological therapies. At the same time, technological advances have made it possible to define, at the cellular and molecular levels, the key pathways that influence the initiation and persistence of chronic inflammatory autoimmune reactions. As our understanding grows, it is likely that this knowledge will be translated into a second generation of biological therapies that are tailor-made for the patient. This review summarizes current perspectives on RA disease pathogenesis, with particular emphasis on what RA T cells look like, what they are likely to see, and how they contribute to persistence of the chronic inflammatory response.
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spelling pubmed-25828132008-11-14 T cells in rheumatoid arthritis Cope, Andrew P Arthritis Res Ther Review Over the past decade and a half, advances in our understanding of the pathogenesis of immune-mediated diseases such as rheumatoid arthritis (RA) have translated directly into benefit for patients. Much of this benefit has arisen through the introduction of targeted biological therapies. At the same time, technological advances have made it possible to define, at the cellular and molecular levels, the key pathways that influence the initiation and persistence of chronic inflammatory autoimmune reactions. As our understanding grows, it is likely that this knowledge will be translated into a second generation of biological therapies that are tailor-made for the patient. This review summarizes current perspectives on RA disease pathogenesis, with particular emphasis on what RA T cells look like, what they are likely to see, and how they contribute to persistence of the chronic inflammatory response. BioMed Central 2008 2008-10-15 /pmc/articles/PMC2582813/ /pubmed/19007421 http://dx.doi.org/10.1186/ar2412 Text en Copyright © 2008 BioMed Central Ltd
spellingShingle Review
Cope, Andrew P
T cells in rheumatoid arthritis
title T cells in rheumatoid arthritis
title_full T cells in rheumatoid arthritis
title_fullStr T cells in rheumatoid arthritis
title_full_unstemmed T cells in rheumatoid arthritis
title_short T cells in rheumatoid arthritis
title_sort t cells in rheumatoid arthritis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2582813/
https://www.ncbi.nlm.nih.gov/pubmed/19007421
http://dx.doi.org/10.1186/ar2412
work_keys_str_mv AT copeandrewp tcellsinrheumatoidarthritis