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Canakinumab as rescue therapy in familial Mediterranean fever refractory to conventional treatment
Familial Mediterranean fever is an autosomal recessive autoinflammatory disorder mainly affecting Mediterranean populations, which is associated with mutations of the MEFV gene that encodes pyrin. Functional studies suggest that pyrin is implicated in the maturation and secretion of interleukin-1 (I...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove Medical Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4408939/ https://www.ncbi.nlm.nih.gov/pubmed/25945034 http://dx.doi.org/10.2147/DDDT.S69117 |
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author | Alpa, Mirella Roccatello, Dario |
author_facet | Alpa, Mirella Roccatello, Dario |
author_sort | Alpa, Mirella |
collection | PubMed |
description | Familial Mediterranean fever is an autosomal recessive autoinflammatory disorder mainly affecting Mediterranean populations, which is associated with mutations of the MEFV gene that encodes pyrin. Functional studies suggest that pyrin is implicated in the maturation and secretion of interleukin-1 (IL-1). The IL-1 receptor antagonist or anti-IL-1 monoclonal antibody may therefore represent a rational approach for the treatment of the rare patients who are refractory to conventional therapy. We report the case of a young female affected by familial Mediterranean fever who proved to be resistant to colchicine and was successfully treated with canakinumab. |
format | Online Article Text |
id | pubmed-4408939 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-44089392015-05-05 Canakinumab as rescue therapy in familial Mediterranean fever refractory to conventional treatment Alpa, Mirella Roccatello, Dario Drug Des Devel Ther Case Report Familial Mediterranean fever is an autosomal recessive autoinflammatory disorder mainly affecting Mediterranean populations, which is associated with mutations of the MEFV gene that encodes pyrin. Functional studies suggest that pyrin is implicated in the maturation and secretion of interleukin-1 (IL-1). The IL-1 receptor antagonist or anti-IL-1 monoclonal antibody may therefore represent a rational approach for the treatment of the rare patients who are refractory to conventional therapy. We report the case of a young female affected by familial Mediterranean fever who proved to be resistant to colchicine and was successfully treated with canakinumab. Dove Medical Press 2015-04-17 /pmc/articles/PMC4408939/ /pubmed/25945034 http://dx.doi.org/10.2147/DDDT.S69117 Text en © 2015 Alpa and Roccatello. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Case Report Alpa, Mirella Roccatello, Dario Canakinumab as rescue therapy in familial Mediterranean fever refractory to conventional treatment |
title | Canakinumab as rescue therapy in familial Mediterranean fever refractory to conventional treatment |
title_full | Canakinumab as rescue therapy in familial Mediterranean fever refractory to conventional treatment |
title_fullStr | Canakinumab as rescue therapy in familial Mediterranean fever refractory to conventional treatment |
title_full_unstemmed | Canakinumab as rescue therapy in familial Mediterranean fever refractory to conventional treatment |
title_short | Canakinumab as rescue therapy in familial Mediterranean fever refractory to conventional treatment |
title_sort | canakinumab as rescue therapy in familial mediterranean fever refractory to conventional treatment |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4408939/ https://www.ncbi.nlm.nih.gov/pubmed/25945034 http://dx.doi.org/10.2147/DDDT.S69117 |
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