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Therapeutic Down-Modulators of Staphylococcal Superantigen-Induced Inflammation and Toxic Shock

Staphylococcal enterotoxin B (SEB) and related superantigenic toxins are potent stimulators of the immune system and cause a variety of diseases in humans, ranging from food poisoning to toxic shock. These toxins bind directly to major histocompatibility complex (MHC) class II molecules on antigen-p...

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Autor principal: Krakauer, Teresa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3153276/
https://www.ncbi.nlm.nih.gov/pubmed/22069668
http://dx.doi.org/10.3390/toxins2081963
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author Krakauer, Teresa
author_facet Krakauer, Teresa
author_sort Krakauer, Teresa
collection PubMed
description Staphylococcal enterotoxin B (SEB) and related superantigenic toxins are potent stimulators of the immune system and cause a variety of diseases in humans, ranging from food poisoning to toxic shock. These toxins bind directly to major histocompatibility complex (MHC) class II molecules on antigen-presenting cells and specific Vβ regions of T-cell receptors (TCR), resulting in hyperactivation of both monocytes/macrophages and T lymphocytes. Activated host cells produce massive amounts of proinflammatory cytokines and chemokines, activating inflammation and coagulation, causing clinical symptoms that include fever, hypotension, and shock. This review summarizes the in vitro and in vivo effects of staphylococcal superantigens, the role of pivotal mediators induced by these toxins in the pathogenic mechanisms of tissue injury, and the therapeutic agents to mitigate the toxic effects of superantigens.
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spelling pubmed-31532762011-11-08 Therapeutic Down-Modulators of Staphylococcal Superantigen-Induced Inflammation and Toxic Shock Krakauer, Teresa Toxins (Basel) Review Staphylococcal enterotoxin B (SEB) and related superantigenic toxins are potent stimulators of the immune system and cause a variety of diseases in humans, ranging from food poisoning to toxic shock. These toxins bind directly to major histocompatibility complex (MHC) class II molecules on antigen-presenting cells and specific Vβ regions of T-cell receptors (TCR), resulting in hyperactivation of both monocytes/macrophages and T lymphocytes. Activated host cells produce massive amounts of proinflammatory cytokines and chemokines, activating inflammation and coagulation, causing clinical symptoms that include fever, hypotension, and shock. This review summarizes the in vitro and in vivo effects of staphylococcal superantigens, the role of pivotal mediators induced by these toxins in the pathogenic mechanisms of tissue injury, and the therapeutic agents to mitigate the toxic effects of superantigens. MDPI 2010-07-29 /pmc/articles/PMC3153276/ /pubmed/22069668 http://dx.doi.org/10.3390/toxins2081963 Text en © 2010 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Krakauer, Teresa
Therapeutic Down-Modulators of Staphylococcal Superantigen-Induced Inflammation and Toxic Shock
title Therapeutic Down-Modulators of Staphylococcal Superantigen-Induced Inflammation and Toxic Shock
title_full Therapeutic Down-Modulators of Staphylococcal Superantigen-Induced Inflammation and Toxic Shock
title_fullStr Therapeutic Down-Modulators of Staphylococcal Superantigen-Induced Inflammation and Toxic Shock
title_full_unstemmed Therapeutic Down-Modulators of Staphylococcal Superantigen-Induced Inflammation and Toxic Shock
title_short Therapeutic Down-Modulators of Staphylococcal Superantigen-Induced Inflammation and Toxic Shock
title_sort therapeutic down-modulators of staphylococcal superantigen-induced inflammation and toxic shock
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3153276/
https://www.ncbi.nlm.nih.gov/pubmed/22069668
http://dx.doi.org/10.3390/toxins2081963
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