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Anakinra treatment for refractory cerebral autoinflammatory responses

Refractory cerebral autoinflammatory–autoimmune diseases are often associated with dysregulated innate immunity and are targeted by anakinra, an interleukin‐1 receptor antagonist. We analyzed the therapeutic effect of anakinra in refractory cerebral autoinflammatory response (CAIR) at a single insti...

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Autores principales: Jang, Yoonhyuk, Lee, Woo‐Jin, Lee, Han Sang, Chu, Kon, Lee, Sang Kun, Lee, Soon‐Tae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8791800/
https://www.ncbi.nlm.nih.gov/pubmed/35040583
http://dx.doi.org/10.1002/acn3.51500
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author Jang, Yoonhyuk
Lee, Woo‐Jin
Lee, Han Sang
Chu, Kon
Lee, Sang Kun
Lee, Soon‐Tae
author_facet Jang, Yoonhyuk
Lee, Woo‐Jin
Lee, Han Sang
Chu, Kon
Lee, Sang Kun
Lee, Soon‐Tae
author_sort Jang, Yoonhyuk
collection PubMed
description Refractory cerebral autoinflammatory–autoimmune diseases are often associated with dysregulated innate immunity and are targeted by anakinra, an interleukin‐1 receptor antagonist. We analyzed the therapeutic effect of anakinra in refractory cerebral autoinflammatory response (CAIR) at a single institution from January 2017 to May 2021. In total, 12 patients with various etiologies were sympathetically treated with anakinra (100 mg/day subcutaneously). Four patients showed good responses, and among these patients, three patients had pathologically demonstrated CAIR. The other eight patients were nonresponsive. No patient had a serious adverse effect. Thus, anakinra may be a therapeutic option for refractory cerebral autoinflammatory diseases.
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spelling pubmed-87918002022-02-04 Anakinra treatment for refractory cerebral autoinflammatory responses Jang, Yoonhyuk Lee, Woo‐Jin Lee, Han Sang Chu, Kon Lee, Sang Kun Lee, Soon‐Tae Ann Clin Transl Neurol Brief Communication Refractory cerebral autoinflammatory–autoimmune diseases are often associated with dysregulated innate immunity and are targeted by anakinra, an interleukin‐1 receptor antagonist. We analyzed the therapeutic effect of anakinra in refractory cerebral autoinflammatory response (CAIR) at a single institution from January 2017 to May 2021. In total, 12 patients with various etiologies were sympathetically treated with anakinra (100 mg/day subcutaneously). Four patients showed good responses, and among these patients, three patients had pathologically demonstrated CAIR. The other eight patients were nonresponsive. No patient had a serious adverse effect. Thus, anakinra may be a therapeutic option for refractory cerebral autoinflammatory diseases. John Wiley and Sons Inc. 2022-01-18 /pmc/articles/PMC8791800/ /pubmed/35040583 http://dx.doi.org/10.1002/acn3.51500 Text en © 2022 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association. 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 Brief Communication
Jang, Yoonhyuk
Lee, Woo‐Jin
Lee, Han Sang
Chu, Kon
Lee, Sang Kun
Lee, Soon‐Tae
Anakinra treatment for refractory cerebral autoinflammatory responses
title Anakinra treatment for refractory cerebral autoinflammatory responses
title_full Anakinra treatment for refractory cerebral autoinflammatory responses
title_fullStr Anakinra treatment for refractory cerebral autoinflammatory responses
title_full_unstemmed Anakinra treatment for refractory cerebral autoinflammatory responses
title_short Anakinra treatment for refractory cerebral autoinflammatory responses
title_sort anakinra treatment for refractory cerebral autoinflammatory responses
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8791800/
https://www.ncbi.nlm.nih.gov/pubmed/35040583
http://dx.doi.org/10.1002/acn3.51500
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