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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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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2005
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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. |
format | Text |
id | pubmed-2833972 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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 |