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Blocking IL-1 in systemic inflammation
A growing number of systemic inflammatory diseases characterized in part by recurrent fevers, leukocytosis, anemia, and elevated acute phase proteins are linked to interleukin (IL)-1 activity since rapid and sustained resolution is observed upon specific blockade of IL-1 receptors. Rapid resolution...
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2005
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2213199/ https://www.ncbi.nlm.nih.gov/pubmed/15867089 http://dx.doi.org/10.1084/jem.20050640 |
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author | Dinarello, Charles A. |
author_facet | Dinarello, Charles A. |
author_sort | Dinarello, Charles A. |
collection | PubMed |
description | A growing number of systemic inflammatory diseases characterized in part by recurrent fevers, leukocytosis, anemia, and elevated acute phase proteins are linked to interleukin (IL)-1 activity since rapid and sustained resolution is observed upon specific blockade of IL-1 receptors. Rapid resolution of systemic and local inflammation is now also reported in systemic onset juvenile idiopathic arthritis (SoJIA). Loss of control of the secretion of IL-1β might be a common mechanism explaining the aberrant activity of IL-1 in these diseases. |
format | Text |
id | pubmed-2213199 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-22131992008-03-11 Blocking IL-1 in systemic inflammation Dinarello, Charles A. J Exp Med Commentary A growing number of systemic inflammatory diseases characterized in part by recurrent fevers, leukocytosis, anemia, and elevated acute phase proteins are linked to interleukin (IL)-1 activity since rapid and sustained resolution is observed upon specific blockade of IL-1 receptors. Rapid resolution of systemic and local inflammation is now also reported in systemic onset juvenile idiopathic arthritis (SoJIA). Loss of control of the secretion of IL-1β might be a common mechanism explaining the aberrant activity of IL-1 in these diseases. The Rockefeller University Press 2005-05-02 /pmc/articles/PMC2213199/ /pubmed/15867089 http://dx.doi.org/10.1084/jem.20050640 Text en Copyright © 2005, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Commentary Dinarello, Charles A. Blocking IL-1 in systemic inflammation |
title | Blocking IL-1 in systemic inflammation |
title_full | Blocking IL-1 in systemic inflammation |
title_fullStr | Blocking IL-1 in systemic inflammation |
title_full_unstemmed | Blocking IL-1 in systemic inflammation |
title_short | Blocking IL-1 in systemic inflammation |
title_sort | blocking il-1 in systemic inflammation |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2213199/ https://www.ncbi.nlm.nih.gov/pubmed/15867089 http://dx.doi.org/10.1084/jem.20050640 |
work_keys_str_mv | AT dinarellocharlesa blockingil1insystemicinflammation |