Healthy subjects express differences in clinical responses to inhaled lipopolysaccharide that are related with inflammation and with atopy

O. Michel, M.A. Dentener, F. Corazza, W.A. Buurman, R. Rylander

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70 Citations (Scopus)

Abstract

Background: Endotoxin and its purified derivative LPS are important contaminants of both domestic and occupational environments that have been related to airway diseases. A body of data suggests that there is considerable interindividual variability in LPS sensitivity. Objective: The aim of the study was to relate the individual clinical responses to inhaled LPS with the inflammatory process and the atopic status. Methods: Fifteen healthy subjects were challenged each week by inhalation,vith saline solution or LPS (0.5, 5, or 50 mug). The systemic response was defined by the increase in body temperature, blood neutrophilia, acute-phase proteins (C-reactive protein and LPS-binding protein [LBP]), and E-selectin. The LPS-induced airway response was defined as the increase in airway responsiveness and related to the cell count and concentration of TNF-alpha, myeloperoxidase, and eosinophil cationic protein in induced sputum. The atopic status was defined as an increase in IgE or a positive skin prick test result. Results: Subjects (n = 7) with a significant increase in body temperature had a larger increase in the systemic inflammatory response (blood neutrophilia; P inflammation.
Original languageEnglish
Pages (from-to)797-804
Number of pages8
JournalJournal of Allergy and Clinical Immunology
Volume107
Issue number5
DOIs
Publication statusPublished - 1 Jan 2001

Cite this

@article{8bcbec3b555c4416b8445ba2471d2929,
title = "Healthy subjects express differences in clinical responses to inhaled lipopolysaccharide that are related with inflammation and with atopy",
abstract = "Background: Endotoxin and its purified derivative LPS are important contaminants of both domestic and occupational environments that have been related to airway diseases. A body of data suggests that there is considerable interindividual variability in LPS sensitivity. Objective: The aim of the study was to relate the individual clinical responses to inhaled LPS with the inflammatory process and the atopic status. Methods: Fifteen healthy subjects were challenged each week by inhalation,vith saline solution or LPS (0.5, 5, or 50 mug). The systemic response was defined by the increase in body temperature, blood neutrophilia, acute-phase proteins (C-reactive protein and LPS-binding protein [LBP]), and E-selectin. The LPS-induced airway response was defined as the increase in airway responsiveness and related to the cell count and concentration of TNF-alpha, myeloperoxidase, and eosinophil cationic protein in induced sputum. The atopic status was defined as an increase in IgE or a positive skin prick test result. Results: Subjects (n = 7) with a significant increase in body temperature had a larger increase in the systemic inflammatory response (blood neutrophilia; P < .01) and in blood concentrations of C-reactive protein (P < .02) and LBP (P < .01). Subjects with a significant increase in airway responsiveness (n = 8) had an increase in the sputum concentration of eosinophil cationic protein (P < .01), The amplitude of the systemic response (increase in body temperature [P < .001], blood neutrophilia [P < .02], and rise in LBP [P < .05] and decrease in FEV, [P < .01]) were inversely associated with the atopic status, suggesting a link between atopy and LPS responsiveness. Conclusions: The clinical response to LPS occurs systemically or locally and is associated with inflammation. The atopic status was inversely related to the systemic inflammation.",
author = "O. Michel and M.A. Dentener and F. Corazza and W.A. Buurman and R. Rylander",
year = "2001",
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doi = "10.1067/mai.2001.114249",
language = "English",
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pages = "797--804",
journal = "Journal of Allergy and Clinical Immunology",
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Healthy subjects express differences in clinical responses to inhaled lipopolysaccharide that are related with inflammation and with atopy. / Michel, O.; Dentener, M.A.; Corazza, F.; Buurman, W.A.; Rylander, R.

In: Journal of Allergy and Clinical Immunology, Vol. 107, No. 5, 01.01.2001, p. 797-804.

Research output: Contribution to journalArticleAcademicpeer-review

TY - JOUR

T1 - Healthy subjects express differences in clinical responses to inhaled lipopolysaccharide that are related with inflammation and with atopy

AU - Michel, O.

AU - Dentener, M.A.

AU - Corazza, F.

AU - Buurman, W.A.

AU - Rylander, R.

PY - 2001/1/1

Y1 - 2001/1/1

N2 - Background: Endotoxin and its purified derivative LPS are important contaminants of both domestic and occupational environments that have been related to airway diseases. A body of data suggests that there is considerable interindividual variability in LPS sensitivity. Objective: The aim of the study was to relate the individual clinical responses to inhaled LPS with the inflammatory process and the atopic status. Methods: Fifteen healthy subjects were challenged each week by inhalation,vith saline solution or LPS (0.5, 5, or 50 mug). The systemic response was defined by the increase in body temperature, blood neutrophilia, acute-phase proteins (C-reactive protein and LPS-binding protein [LBP]), and E-selectin. The LPS-induced airway response was defined as the increase in airway responsiveness and related to the cell count and concentration of TNF-alpha, myeloperoxidase, and eosinophil cationic protein in induced sputum. The atopic status was defined as an increase in IgE or a positive skin prick test result. Results: Subjects (n = 7) with a significant increase in body temperature had a larger increase in the systemic inflammatory response (blood neutrophilia; P < .01) and in blood concentrations of C-reactive protein (P < .02) and LBP (P < .01). Subjects with a significant increase in airway responsiveness (n = 8) had an increase in the sputum concentration of eosinophil cationic protein (P < .01), The amplitude of the systemic response (increase in body temperature [P < .001], blood neutrophilia [P < .02], and rise in LBP [P < .05] and decrease in FEV, [P < .01]) were inversely associated with the atopic status, suggesting a link between atopy and LPS responsiveness. Conclusions: The clinical response to LPS occurs systemically or locally and is associated with inflammation. The atopic status was inversely related to the systemic inflammation.

AB - Background: Endotoxin and its purified derivative LPS are important contaminants of both domestic and occupational environments that have been related to airway diseases. A body of data suggests that there is considerable interindividual variability in LPS sensitivity. Objective: The aim of the study was to relate the individual clinical responses to inhaled LPS with the inflammatory process and the atopic status. Methods: Fifteen healthy subjects were challenged each week by inhalation,vith saline solution or LPS (0.5, 5, or 50 mug). The systemic response was defined by the increase in body temperature, blood neutrophilia, acute-phase proteins (C-reactive protein and LPS-binding protein [LBP]), and E-selectin. The LPS-induced airway response was defined as the increase in airway responsiveness and related to the cell count and concentration of TNF-alpha, myeloperoxidase, and eosinophil cationic protein in induced sputum. The atopic status was defined as an increase in IgE or a positive skin prick test result. Results: Subjects (n = 7) with a significant increase in body temperature had a larger increase in the systemic inflammatory response (blood neutrophilia; P < .01) and in blood concentrations of C-reactive protein (P < .02) and LBP (P < .01). Subjects with a significant increase in airway responsiveness (n = 8) had an increase in the sputum concentration of eosinophil cationic protein (P < .01), The amplitude of the systemic response (increase in body temperature [P < .001], blood neutrophilia [P < .02], and rise in LBP [P < .05] and decrease in FEV, [P < .01]) were inversely associated with the atopic status, suggesting a link between atopy and LPS responsiveness. Conclusions: The clinical response to LPS occurs systemically or locally and is associated with inflammation. The atopic status was inversely related to the systemic inflammation.

U2 - 10.1067/mai.2001.114249

DO - 10.1067/mai.2001.114249

M3 - Article

VL - 107

SP - 797

EP - 804

JO - Journal of Allergy and Clinical Immunology

JF - Journal of Allergy and Clinical Immunology

SN - 0091-6749

IS - 5

ER -