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Rituximab for the treatment of refractory anti-glomerular basement membrane disease
BACKGROUND: Anti-glomerular basement membrane (anti-GBM) disease is a rare but severe autoantibody-mediated immune disorder. The typical clinical presentation includes rapidly progressive glomerulonephritis and often concurrent pulmonary hemorrhage. The present study is aimed to investigate the ther...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291707/ https://www.ncbi.nlm.nih.gov/pubmed/35820833 http://dx.doi.org/10.1080/0886022X.2022.2097405 |
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author | Yang, Xue-Fen Jia, Xiao-Yu Yu, Xiao-Juan Cui, Zhao Zhao, Ming-Hui |
author_facet | Yang, Xue-Fen Jia, Xiao-Yu Yu, Xiao-Juan Cui, Zhao Zhao, Ming-Hui |
author_sort | Yang, Xue-Fen |
collection | PubMed |
description | BACKGROUND: Anti-glomerular basement membrane (anti-GBM) disease is a rare but severe autoantibody-mediated immune disorder. The typical clinical presentation includes rapidly progressive glomerulonephritis and often concurrent pulmonary hemorrhage. The present study is aimed to investigate the therapeutic effects of rituximab either used alone or with other immunosuppressants. METHODS: Eight patients diagnosed with anti-GBM disease and treated with rituximab from 2014 to 2020 were retrospectively reviewed. RESULTS: Eight patients included 5 males and 3 females with a median age of 58.5 years. They all presented severe kidney injuries and 1 patient had lung hemorrhage. At diagnosis, the median of serum creatinine was 246 µmol/L (ranging from 91 to 850 µmol/L), with 3 patients requiring dialysis. All of them received corticosteroids and plasmapheresis. Rituximab was given as either standard four weekly doses or one pulse ranging from 100 to 600 mg. After a median follow-up of 34.5 months, kidney function was partially recovered or stabilized in 5/8 (62.5%) patients, free of dialysis. Anti-GBM antibodies remained undetected in all patients during follow-up. No severe adverse effect associated with rituximab was observed. CONCLUSION: Rituximab may be an alternative therapy in the treatment of patient with severe or refractory anti-GBM disease. |
format | Online Article Text |
id | pubmed-9291707 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-92917072022-07-19 Rituximab for the treatment of refractory anti-glomerular basement membrane disease Yang, Xue-Fen Jia, Xiao-Yu Yu, Xiao-Juan Cui, Zhao Zhao, Ming-Hui Ren Fail Clinical Studies BACKGROUND: Anti-glomerular basement membrane (anti-GBM) disease is a rare but severe autoantibody-mediated immune disorder. The typical clinical presentation includes rapidly progressive glomerulonephritis and often concurrent pulmonary hemorrhage. The present study is aimed to investigate the therapeutic effects of rituximab either used alone or with other immunosuppressants. METHODS: Eight patients diagnosed with anti-GBM disease and treated with rituximab from 2014 to 2020 were retrospectively reviewed. RESULTS: Eight patients included 5 males and 3 females with a median age of 58.5 years. They all presented severe kidney injuries and 1 patient had lung hemorrhage. At diagnosis, the median of serum creatinine was 246 µmol/L (ranging from 91 to 850 µmol/L), with 3 patients requiring dialysis. All of them received corticosteroids and plasmapheresis. Rituximab was given as either standard four weekly doses or one pulse ranging from 100 to 600 mg. After a median follow-up of 34.5 months, kidney function was partially recovered or stabilized in 5/8 (62.5%) patients, free of dialysis. Anti-GBM antibodies remained undetected in all patients during follow-up. No severe adverse effect associated with rituximab was observed. CONCLUSION: Rituximab may be an alternative therapy in the treatment of patient with severe or refractory anti-GBM disease. Taylor & Francis 2022-07-12 /pmc/articles/PMC9291707/ /pubmed/35820833 http://dx.doi.org/10.1080/0886022X.2022.2097405 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Studies Yang, Xue-Fen Jia, Xiao-Yu Yu, Xiao-Juan Cui, Zhao Zhao, Ming-Hui Rituximab for the treatment of refractory anti-glomerular basement membrane disease |
title | Rituximab for the treatment of refractory anti-glomerular basement membrane disease |
title_full | Rituximab for the treatment of refractory anti-glomerular basement membrane disease |
title_fullStr | Rituximab for the treatment of refractory anti-glomerular basement membrane disease |
title_full_unstemmed | Rituximab for the treatment of refractory anti-glomerular basement membrane disease |
title_short | Rituximab for the treatment of refractory anti-glomerular basement membrane disease |
title_sort | rituximab for the treatment of refractory anti-glomerular basement membrane disease |
topic | Clinical Studies |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291707/ https://www.ncbi.nlm.nih.gov/pubmed/35820833 http://dx.doi.org/10.1080/0886022X.2022.2097405 |
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