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A recombinant human receptor antagonist to interleukin 1 improves survival after lethal endotoxemia in mice
Interleukin 1 (IL-1) is an endogenously produced cytokine that mediates a variety of physiological effects that may be beneficial or deleterious to the host. C57Bl/6 mice treated intravenously with a recently characterized human recombinant receptor antagonist protein to IL-1 (IL-1ra) had improved s...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1991
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2190820/ https://www.ncbi.nlm.nih.gov/pubmed/1826127 |
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collection | PubMed |
description | Interleukin 1 (IL-1) is an endogenously produced cytokine that mediates a variety of physiological effects that may be beneficial or deleterious to the host. C57Bl/6 mice treated intravenously with a recently characterized human recombinant receptor antagonist protein to IL-1 (IL-1ra) had improved survival when treated after a lethal Escherichia coli endotoxin (lipopolysaccharide [LPS]) challenge. IL-1ra was effective when treatment was initiated after LPS, and intravenous administration every 4 h for 24 h was required. Serum levels of tumor necrosis factor (TNF) activity after LPS and in vitro TNF cytotoxicity were not altered by treatment with IL-1ra. These experiments provide direct evidence that the lethal effects of LPS may be mediated through the action of IL-1 and that the IL-1ra can provide a new treatment strategy for disease processes mediated via this cytokine. |
format | Text |
id | pubmed-2190820 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1991 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21908202008-04-17 A recombinant human receptor antagonist to interleukin 1 improves survival after lethal endotoxemia in mice J Exp Med Articles Interleukin 1 (IL-1) is an endogenously produced cytokine that mediates a variety of physiological effects that may be beneficial or deleterious to the host. C57Bl/6 mice treated intravenously with a recently characterized human recombinant receptor antagonist protein to IL-1 (IL-1ra) had improved survival when treated after a lethal Escherichia coli endotoxin (lipopolysaccharide [LPS]) challenge. IL-1ra was effective when treatment was initiated after LPS, and intravenous administration every 4 h for 24 h was required. Serum levels of tumor necrosis factor (TNF) activity after LPS and in vitro TNF cytotoxicity were not altered by treatment with IL-1ra. These experiments provide direct evidence that the lethal effects of LPS may be mediated through the action of IL-1 and that the IL-1ra can provide a new treatment strategy for disease processes mediated via this cytokine. The Rockefeller University Press 1991-04-01 /pmc/articles/PMC2190820/ /pubmed/1826127 Text en 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 | Articles A recombinant human receptor antagonist to interleukin 1 improves survival after lethal endotoxemia in mice |
title | A recombinant human receptor antagonist to interleukin 1 improves survival after lethal endotoxemia in mice |
title_full | A recombinant human receptor antagonist to interleukin 1 improves survival after lethal endotoxemia in mice |
title_fullStr | A recombinant human receptor antagonist to interleukin 1 improves survival after lethal endotoxemia in mice |
title_full_unstemmed | A recombinant human receptor antagonist to interleukin 1 improves survival after lethal endotoxemia in mice |
title_short | A recombinant human receptor antagonist to interleukin 1 improves survival after lethal endotoxemia in mice |
title_sort | recombinant human receptor antagonist to interleukin 1 improves survival after lethal endotoxemia in mice |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2190820/ https://www.ncbi.nlm.nih.gov/pubmed/1826127 |