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Treatment of Multiorgan Sarcoidosis With Tofacitinib
OBJECTIVE: Sarcoidosis is an idiopathic inflammatory disorder that is difficult to treat. There is accumulating evidence that constitutive activation of Janus kinase–signal transducer and activator of transcription (JAK‐STAT) signaling occurs in sarcoidosis and represents a target for treatment. Her...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7011417/ https://www.ncbi.nlm.nih.gov/pubmed/31916703 http://dx.doi.org/10.1002/acr2.11112 |
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author | Damsky, William Young, Bryan D. Sloan, Brett Miller, Edward J. Obando, J. Antonio King, Brett |
author_facet | Damsky, William Young, Bryan D. Sloan, Brett Miller, Edward J. Obando, J. Antonio King, Brett |
author_sort | Damsky, William |
collection | PubMed |
description | OBJECTIVE: Sarcoidosis is an idiopathic inflammatory disorder that is difficult to treat. There is accumulating evidence that constitutive activation of Janus kinase–signal transducer and activator of transcription (JAK‐STAT) signaling occurs in sarcoidosis and represents a target for treatment. Here we report the efficacy of tofacitinib, a Janus kinase (JAK) inhibitor, in a single patient with multiorgan sarcoidosis. METHODS: A patient with long‐standing multiorgan sarcoidosis who was unresponsive to other commonly used therapies, including methotrexate, prednisone, and tumor necrosis factor α blockade, was treated with tofacitinib. RESULTS: Tofacitinib treatment resulted in clinical remission of cutaneous sarcoidosis lesions and resolution of positron emission tomography avid lesions in internal organs after 6 months. An evaluation of lesional tissue and blood before and during treatment showed resolution of granulomatous inflammation and normalization of disease biomarkers. CONCLUSION: This case illustrates the promise of JAK inhibition as a strategy to treat recalcitrant sarcoidosis and suggests that further study of JAK inhibitors in sarcoidosis is needed. |
format | Online Article Text |
id | pubmed-7011417 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70114172020-02-18 Treatment of Multiorgan Sarcoidosis With Tofacitinib Damsky, William Young, Bryan D. Sloan, Brett Miller, Edward J. Obando, J. Antonio King, Brett ACR Open Rheumatol Brief Report OBJECTIVE: Sarcoidosis is an idiopathic inflammatory disorder that is difficult to treat. There is accumulating evidence that constitutive activation of Janus kinase–signal transducer and activator of transcription (JAK‐STAT) signaling occurs in sarcoidosis and represents a target for treatment. Here we report the efficacy of tofacitinib, a Janus kinase (JAK) inhibitor, in a single patient with multiorgan sarcoidosis. METHODS: A patient with long‐standing multiorgan sarcoidosis who was unresponsive to other commonly used therapies, including methotrexate, prednisone, and tumor necrosis factor α blockade, was treated with tofacitinib. RESULTS: Tofacitinib treatment resulted in clinical remission of cutaneous sarcoidosis lesions and resolution of positron emission tomography avid lesions in internal organs after 6 months. An evaluation of lesional tissue and blood before and during treatment showed resolution of granulomatous inflammation and normalization of disease biomarkers. CONCLUSION: This case illustrates the promise of JAK inhibition as a strategy to treat recalcitrant sarcoidosis and suggests that further study of JAK inhibitors in sarcoidosis is needed. John Wiley and Sons Inc. 2020-01-09 /pmc/articles/PMC7011417/ /pubmed/31916703 http://dx.doi.org/10.1002/acr2.11112 Text en © 2020 The Authors. ACR Open Rheumatology published by Wiley Periodicals, Inc. on behalf of American College of Rheumatology. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Brief Report Damsky, William Young, Bryan D. Sloan, Brett Miller, Edward J. Obando, J. Antonio King, Brett Treatment of Multiorgan Sarcoidosis With Tofacitinib |
title | Treatment of Multiorgan Sarcoidosis With Tofacitinib |
title_full | Treatment of Multiorgan Sarcoidosis With Tofacitinib |
title_fullStr | Treatment of Multiorgan Sarcoidosis With Tofacitinib |
title_full_unstemmed | Treatment of Multiorgan Sarcoidosis With Tofacitinib |
title_short | Treatment of Multiorgan Sarcoidosis With Tofacitinib |
title_sort | treatment of multiorgan sarcoidosis with tofacitinib |
topic | Brief Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7011417/ https://www.ncbi.nlm.nih.gov/pubmed/31916703 http://dx.doi.org/10.1002/acr2.11112 |
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