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Staphylococcus aureus enterotoxins induce IL-8 secretion by human nasal epithelial cells
BACKGROUND: Staphylococcus aureus produces a set of proteins which act both as superantigens and toxins. Although their mode of action as superantigens is well understood, little is known about their effects on airway epithelial cells. METHODS: To investigate this problem, primary nasal epithelial c...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1579218/ https://www.ncbi.nlm.nih.gov/pubmed/16952309 http://dx.doi.org/10.1186/1465-9921-7-115 |
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author | O'Brien, Garrett J Riddell, Gareth Elborn, J Stuart Ennis, Madeleine Skibinski, Grzegorz |
author_facet | O'Brien, Garrett J Riddell, Gareth Elborn, J Stuart Ennis, Madeleine Skibinski, Grzegorz |
author_sort | O'Brien, Garrett J |
collection | PubMed |
description | BACKGROUND: Staphylococcus aureus produces a set of proteins which act both as superantigens and toxins. Although their mode of action as superantigens is well understood, little is known about their effects on airway epithelial cells. METHODS: To investigate this problem, primary nasal epithelial cells derived from normal and asthmatic subjects were stimulated with staphylococcal enterotoxin A and B (SEA and SEB) and secreted (supernatants) and cell-associated (cell lysates) IL-8, TNF-α, RANTES and eotaxin were determined by specific ELISAs. RESULTS: Non-toxic concentrations of SEA and SEB (0.01 μg/ml and 1.0 μg/ml) induced IL-8 secretion after 24 h of culture. Pre-treatment of the cells with IFN-γ (50 IU/ml) resulted in a further increase of IL-8 secretion. In cells from healthy donors pretreated with IFN-γ, SEA at 1.0 μg/ml induced release of 1009 pg/ml IL-8 (733.0–1216 pg/ml, median (range)) while in cells from asthmatic donors the same treatment induced significantly higher IL-8 secretion – 1550 pg/ml (1168.0–2000.0 pg/ml p = 0.04). Normal cells pre-treated with IFN-γ and then cultured with SEB at 1.0 μg/ml released 904.6 pg/ml IL-8 (666.5–1169.0 pg/ml). Cells from asthmatics treated in the same way produced significantly higher amounts of IL-8 – 1665.0 pg/ml (1168.0–2000.0 pg/ml, p = 0.01). Blocking antibodies to MHC class II molecules added to cultures stimulated with SEA and SEB, reduced IL-8 secretion by about 40% in IFN-γ unstimulated cultures and 75% in IFN-γ stimulated cultures. No secretion of TNF-α, RANTES and eotaxin was noted. CONCLUSION: Staphylococcal enterotoxins may have a role in the pathogenesis of asthma. |
format | Text |
id | pubmed-1579218 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-15792182006-09-28 Staphylococcus aureus enterotoxins induce IL-8 secretion by human nasal epithelial cells O'Brien, Garrett J Riddell, Gareth Elborn, J Stuart Ennis, Madeleine Skibinski, Grzegorz Respir Res Research BACKGROUND: Staphylococcus aureus produces a set of proteins which act both as superantigens and toxins. Although their mode of action as superantigens is well understood, little is known about their effects on airway epithelial cells. METHODS: To investigate this problem, primary nasal epithelial cells derived from normal and asthmatic subjects were stimulated with staphylococcal enterotoxin A and B (SEA and SEB) and secreted (supernatants) and cell-associated (cell lysates) IL-8, TNF-α, RANTES and eotaxin were determined by specific ELISAs. RESULTS: Non-toxic concentrations of SEA and SEB (0.01 μg/ml and 1.0 μg/ml) induced IL-8 secretion after 24 h of culture. Pre-treatment of the cells with IFN-γ (50 IU/ml) resulted in a further increase of IL-8 secretion. In cells from healthy donors pretreated with IFN-γ, SEA at 1.0 μg/ml induced release of 1009 pg/ml IL-8 (733.0–1216 pg/ml, median (range)) while in cells from asthmatic donors the same treatment induced significantly higher IL-8 secretion – 1550 pg/ml (1168.0–2000.0 pg/ml p = 0.04). Normal cells pre-treated with IFN-γ and then cultured with SEB at 1.0 μg/ml released 904.6 pg/ml IL-8 (666.5–1169.0 pg/ml). Cells from asthmatics treated in the same way produced significantly higher amounts of IL-8 – 1665.0 pg/ml (1168.0–2000.0 pg/ml, p = 0.01). Blocking antibodies to MHC class II molecules added to cultures stimulated with SEA and SEB, reduced IL-8 secretion by about 40% in IFN-γ unstimulated cultures and 75% in IFN-γ stimulated cultures. No secretion of TNF-α, RANTES and eotaxin was noted. CONCLUSION: Staphylococcal enterotoxins may have a role in the pathogenesis of asthma. BioMed Central 2006 2006-09-04 /pmc/articles/PMC1579218/ /pubmed/16952309 http://dx.doi.org/10.1186/1465-9921-7-115 Text en Copyright © 2006 O'Brien et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research O'Brien, Garrett J Riddell, Gareth Elborn, J Stuart Ennis, Madeleine Skibinski, Grzegorz Staphylococcus aureus enterotoxins induce IL-8 secretion by human nasal epithelial cells |
title | Staphylococcus aureus enterotoxins induce IL-8 secretion by human nasal epithelial cells |
title_full | Staphylococcus aureus enterotoxins induce IL-8 secretion by human nasal epithelial cells |
title_fullStr | Staphylococcus aureus enterotoxins induce IL-8 secretion by human nasal epithelial cells |
title_full_unstemmed | Staphylococcus aureus enterotoxins induce IL-8 secretion by human nasal epithelial cells |
title_short | Staphylococcus aureus enterotoxins induce IL-8 secretion by human nasal epithelial cells |
title_sort | staphylococcus aureus enterotoxins induce il-8 secretion by human nasal epithelial cells |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1579218/ https://www.ncbi.nlm.nih.gov/pubmed/16952309 http://dx.doi.org/10.1186/1465-9921-7-115 |
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