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Abatacept in the treatment of rheumatoid arthritis

T-cell biology has regained importance in the pathogenesis of rheumatoid arthritis. Despite the significant improvements associated with the introduction of tumor necrosis factor-α blockade, reasonable proportions of failures and suboptimal responses have been reported, necessitating a search for al...

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Detalles Bibliográficos
Autores principales: Buch, Maya H, Vital, Edward M, Emery, Paul
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2582812/
https://www.ncbi.nlm.nih.gov/pubmed/19007425
http://dx.doi.org/10.1186/ar2416
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author Buch, Maya H
Vital, Edward M
Emery, Paul
author_facet Buch, Maya H
Vital, Edward M
Emery, Paul
author_sort Buch, Maya H
collection PubMed
description T-cell biology has regained importance in the pathogenesis of rheumatoid arthritis. Despite the significant improvements associated with the introduction of tumor necrosis factor-α blockade, reasonable proportions of failures and suboptimal responses have been reported, necessitating a search for alternative targeted therapies. This has included drug therapy designed to interrupt T-cell activation via the co-stimulation pathway. Abatacept is a recombinant fusion protein that blocks the co-stimulatory signal mediated by the CD28-CD80/86 pathway, which is required for T-cell activation. Several clinical trials have confirmed the safety and efficacy of this drug in the treatment of rheumatoid arthritis. This review summarizes the clinical data supporting this line of treatment and considers the safety and efficacy data from phase II and III trials.
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spelling pubmed-25828122008-11-14 Abatacept in the treatment of rheumatoid arthritis Buch, Maya H Vital, Edward M Emery, Paul Arthritis Res Ther Review T-cell biology has regained importance in the pathogenesis of rheumatoid arthritis. Despite the significant improvements associated with the introduction of tumor necrosis factor-α blockade, reasonable proportions of failures and suboptimal responses have been reported, necessitating a search for alternative targeted therapies. This has included drug therapy designed to interrupt T-cell activation via the co-stimulation pathway. Abatacept is a recombinant fusion protein that blocks the co-stimulatory signal mediated by the CD28-CD80/86 pathway, which is required for T-cell activation. Several clinical trials have confirmed the safety and efficacy of this drug in the treatment of rheumatoid arthritis. This review summarizes the clinical data supporting this line of treatment and considers the safety and efficacy data from phase II and III trials. BioMed Central 2008 2008-10-15 /pmc/articles/PMC2582812/ /pubmed/19007425 http://dx.doi.org/10.1186/ar2416 Text en Copyright © 2008 BioMed Central Ltd
spellingShingle Review
Buch, Maya H
Vital, Edward M
Emery, Paul
Abatacept in the treatment of rheumatoid arthritis
title Abatacept in the treatment of rheumatoid arthritis
title_full Abatacept in the treatment of rheumatoid arthritis
title_fullStr Abatacept in the treatment of rheumatoid arthritis
title_full_unstemmed Abatacept in the treatment of rheumatoid arthritis
title_short Abatacept in the treatment of rheumatoid arthritis
title_sort abatacept in the treatment of rheumatoid arthritis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2582812/
https://www.ncbi.nlm.nih.gov/pubmed/19007425
http://dx.doi.org/10.1186/ar2416
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