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B cell targeted therapies

Although the precise pathogenesis of rheumatoid arthritis (RA) remains unclear, many cell populations, including monocytes, macrophages, endothelial cells, fibroblasts and B cells, participate in the inflammatory process. Ongoing research continues to evaluate the critical roles played by B cells in...

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Detalles Bibliográficos
Autor principal: Keystone, Edward
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2833972/
https://www.ncbi.nlm.nih.gov/pubmed/15960817
http://dx.doi.org/10.1186/ar1738
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author Keystone, Edward
author_facet Keystone, Edward
author_sort Keystone, Edward
collection PubMed
description Although the precise pathogenesis of rheumatoid arthritis (RA) remains unclear, many cell populations, including monocytes, macrophages, endothelial cells, fibroblasts and B cells, participate in the inflammatory process. Ongoing research continues to evaluate the critical roles played by B cells in sustaining the chronic inflammatory process of RA. These findings have contributed to the development of targeted therapies that deplete B cells, such as rituximab, as well as inhibitors of B lymphocyte stimulation, such as belimumab. In a phase I trial, belimumab treatment significantly reduced CD20(+ )levels in patients with systemic lupus erythematosus. Phase I and phase II trials of rituximab found that rituximab plus methotrexate achieved significantly better American College of Rheumatology 50% responses for patients with RA than those patients receiving monotherapy with methotrexate. These clinical trial data present promising evidence for B cell targeted therapies as future therapeutic options for RA.
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spelling pubmed-28339722010-03-08 B cell targeted therapies Keystone, Edward Arthritis Res Ther Review Although the precise pathogenesis of rheumatoid arthritis (RA) remains unclear, many cell populations, including monocytes, macrophages, endothelial cells, fibroblasts and B cells, participate in the inflammatory process. Ongoing research continues to evaluate the critical roles played by B cells in sustaining the chronic inflammatory process of RA. These findings have contributed to the development of targeted therapies that deplete B cells, such as rituximab, as well as inhibitors of B lymphocyte stimulation, such as belimumab. In a phase I trial, belimumab treatment significantly reduced CD20(+ )levels in patients with systemic lupus erythematosus. Phase I and phase II trials of rituximab found that rituximab plus methotrexate achieved significantly better American College of Rheumatology 50% responses for patients with RA than those patients receiving monotherapy with methotrexate. These clinical trial data present promising evidence for B cell targeted therapies as future therapeutic options for RA. BioMed Central 2005 2005-05-18 /pmc/articles/PMC2833972/ /pubmed/15960817 http://dx.doi.org/10.1186/ar1738 Text en Copyright ©2005 BioMed Central Ltd
spellingShingle Review
Keystone, Edward
B cell targeted therapies
title B cell targeted therapies
title_full B cell targeted therapies
title_fullStr B cell targeted therapies
title_full_unstemmed B cell targeted therapies
title_short B cell targeted therapies
title_sort b cell targeted therapies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2833972/
https://www.ncbi.nlm.nih.gov/pubmed/15960817
http://dx.doi.org/10.1186/ar1738
work_keys_str_mv AT keystoneedward bcelltargetedtherapies