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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...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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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. |
format | Text |
id | pubmed-2582812 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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