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Efficacy, safety, and tolerability of abatacept in the management of rheumatoid arthritis

The management of rheumatoid arthritis (RA) has undergone an impressive transformation over the past few decades. Further understanding of the pathophysiology of the disease process has resulted in the development of biologic agents that target proinflammatory cytokines and both B and T lymphocytes....

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Detalles Bibliográficos
Autor principal: Lutt, Joseph R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5074723/
https://www.ncbi.nlm.nih.gov/pubmed/27789979
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author Lutt, Joseph R
author_facet Lutt, Joseph R
author_sort Lutt, Joseph R
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description The management of rheumatoid arthritis (RA) has undergone an impressive transformation over the past few decades. Further understanding of the pathophysiology of the disease process has resulted in the development of biologic agents that target proinflammatory cytokines and both B and T lymphocytes. By blocking an important costimulatory pathway, abatacept leads to a dramatic reduction in T cell stimulation and proliferation. Multiple clinical trials have revealed consistent benefit with regards to clinical and radiographic efficacy, quality of life, and disability in patients suffering from RA who have had inadequate responses to methotrexate or tumor necrosis factor inhibitors. The possibility of remission when used early in the disease course has also been demonstrated. Importantly, abatacept has been very well tolerated with a low rate of serious infections and no apparent increase in malignancies to date. Continued surveillance of the benefits and risks will help to better define its place amongst the other biologic agents in the treatment of RA.
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spelling pubmed-50747232016-10-27 Efficacy, safety, and tolerability of abatacept in the management of rheumatoid arthritis Lutt, Joseph R Open Access Rheumatol Review The management of rheumatoid arthritis (RA) has undergone an impressive transformation over the past few decades. Further understanding of the pathophysiology of the disease process has resulted in the development of biologic agents that target proinflammatory cytokines and both B and T lymphocytes. By blocking an important costimulatory pathway, abatacept leads to a dramatic reduction in T cell stimulation and proliferation. Multiple clinical trials have revealed consistent benefit with regards to clinical and radiographic efficacy, quality of life, and disability in patients suffering from RA who have had inadequate responses to methotrexate or tumor necrosis factor inhibitors. The possibility of remission when used early in the disease course has also been demonstrated. Importantly, abatacept has been very well tolerated with a low rate of serious infections and no apparent increase in malignancies to date. Continued surveillance of the benefits and risks will help to better define its place amongst the other biologic agents in the treatment of RA. Dove Medical Press 2009-05-08 /pmc/articles/PMC5074723/ /pubmed/27789979 Text en © 2009 Lutt, publisher and licensee Dove Medical Press Ltd This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Review
Lutt, Joseph R
Efficacy, safety, and tolerability of abatacept in the management of rheumatoid arthritis
title Efficacy, safety, and tolerability of abatacept in the management of rheumatoid arthritis
title_full Efficacy, safety, and tolerability of abatacept in the management of rheumatoid arthritis
title_fullStr Efficacy, safety, and tolerability of abatacept in the management of rheumatoid arthritis
title_full_unstemmed Efficacy, safety, and tolerability of abatacept in the management of rheumatoid arthritis
title_short Efficacy, safety, and tolerability of abatacept in the management of rheumatoid arthritis
title_sort efficacy, safety, and tolerability of abatacept in the management of rheumatoid arthritis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5074723/
https://www.ncbi.nlm.nih.gov/pubmed/27789979
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