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Concomitant use of dupilumab with glucocorticoid in bullous pemphigoid reduces disease severity: A preliminary study
OBJECTIVE: To retrospectively analyze the efficacy and safety of dupilumab in the treatment of bullous pemphigoid. METHODS: From October 2020 to October 2022, the medical records of patients with bullous pemphigoid who were treated with dupilumab in our department were collected retrospectively to a...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10367446/ https://www.ncbi.nlm.nih.gov/pubmed/37506153 http://dx.doi.org/10.1002/iid3.924 |
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author | Hu, Lingyu Huang, Ruiting Jiang, Fuqiong You, Shuqiong Wu, Qian |
author_facet | Hu, Lingyu Huang, Ruiting Jiang, Fuqiong You, Shuqiong Wu, Qian |
author_sort | Hu, Lingyu |
collection | PubMed |
description | OBJECTIVE: To retrospectively analyze the efficacy and safety of dupilumab in the treatment of bullous pemphigoid. METHODS: From October 2020 to October 2022, the medical records of patients with bullous pemphigoid who were treated with dupilumab in our department were collected retrospectively to analyze the therapeutic effect and changes in laboratory indexes. RESULTS: The records of a total of 11 patients with bullous pemphigoid who were treated with dupilumab was reviewed. Within 2 weeks of the treatment, 10 (90.9%) of the 11 patients had complete or substantial control of the disease. The BPDAI scores of the patients decreased from baseline 113 (62, 181) to 37 (6, 130) at 2 weeks (p = .001) and 4 (0, 37) at 12 weeks after treatment (p < .001). In the 11 patients treated with dupilumab, the relief time of pruritus was 0–3 days (0.5, 7) days, and the pruritus was significantly alleviated after 2 weeks (t = 15.925, p < .001). The DLQI score decreased from (25.5 ± 2.5) before treatment, to (11.8 ± 4.4) at 2 weeks (t = 10.764, p < .001) and (2.1 ± 1.9) at 12 weeks (t = 30.038, p < .001). The patients had high eosinophil counts, high serum IgE levels, low serum total protein levels, and abnormal blood coagulation function. The aforementioned indicators gradually returned to normal after treatment. No adverse reactions occurred during the treatment. CONCLUSION: Dupilumab can effectively control the condition of bullous pemphigoid, efficiently relieve pruritus symptoms, and is relatively safe. |
format | Online Article Text |
id | pubmed-10367446 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-103674462023-07-26 Concomitant use of dupilumab with glucocorticoid in bullous pemphigoid reduces disease severity: A preliminary study Hu, Lingyu Huang, Ruiting Jiang, Fuqiong You, Shuqiong Wu, Qian Immun Inflamm Dis Original Articles OBJECTIVE: To retrospectively analyze the efficacy and safety of dupilumab in the treatment of bullous pemphigoid. METHODS: From October 2020 to October 2022, the medical records of patients with bullous pemphigoid who were treated with dupilumab in our department were collected retrospectively to analyze the therapeutic effect and changes in laboratory indexes. RESULTS: The records of a total of 11 patients with bullous pemphigoid who were treated with dupilumab was reviewed. Within 2 weeks of the treatment, 10 (90.9%) of the 11 patients had complete or substantial control of the disease. The BPDAI scores of the patients decreased from baseline 113 (62, 181) to 37 (6, 130) at 2 weeks (p = .001) and 4 (0, 37) at 12 weeks after treatment (p < .001). In the 11 patients treated with dupilumab, the relief time of pruritus was 0–3 days (0.5, 7) days, and the pruritus was significantly alleviated after 2 weeks (t = 15.925, p < .001). The DLQI score decreased from (25.5 ± 2.5) before treatment, to (11.8 ± 4.4) at 2 weeks (t = 10.764, p < .001) and (2.1 ± 1.9) at 12 weeks (t = 30.038, p < .001). The patients had high eosinophil counts, high serum IgE levels, low serum total protein levels, and abnormal blood coagulation function. The aforementioned indicators gradually returned to normal after treatment. No adverse reactions occurred during the treatment. CONCLUSION: Dupilumab can effectively control the condition of bullous pemphigoid, efficiently relieve pruritus symptoms, and is relatively safe. John Wiley and Sons Inc. 2023-07-25 /pmc/articles/PMC10367446/ /pubmed/37506153 http://dx.doi.org/10.1002/iid3.924 Text en © 2023 The Authors. Immunity, Inflammation and Disease published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Hu, Lingyu Huang, Ruiting Jiang, Fuqiong You, Shuqiong Wu, Qian Concomitant use of dupilumab with glucocorticoid in bullous pemphigoid reduces disease severity: A preliminary study |
title | Concomitant use of dupilumab with glucocorticoid in bullous pemphigoid reduces disease severity: A preliminary study |
title_full | Concomitant use of dupilumab with glucocorticoid in bullous pemphigoid reduces disease severity: A preliminary study |
title_fullStr | Concomitant use of dupilumab with glucocorticoid in bullous pemphigoid reduces disease severity: A preliminary study |
title_full_unstemmed | Concomitant use of dupilumab with glucocorticoid in bullous pemphigoid reduces disease severity: A preliminary study |
title_short | Concomitant use of dupilumab with glucocorticoid in bullous pemphigoid reduces disease severity: A preliminary study |
title_sort | concomitant use of dupilumab with glucocorticoid in bullous pemphigoid reduces disease severity: a preliminary study |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10367446/ https://www.ncbi.nlm.nih.gov/pubmed/37506153 http://dx.doi.org/10.1002/iid3.924 |
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