Involvement of Cytokines in the Pathogenesis of Hypersensitivity Pneumonitis: Evaluation of Immunotherapeutic Measures in a Mouse Model

C57BL/6 inbred strain mice were instilled intranasally with 150 μg/day of the actinomycete Faeni rectivirgula three days a week as a model of farmer's lung disease. Instilled mice developed a strong alveolitis manifested by a large increase in the number of cells in the bronchoalveolar lavage (...

Full description

Saved in:
Bibliographic Details
Main Authors: Michel Denis, Marie Bédard, Jacques Gagnon, Yvon Cormier, Michel Laviolette
Format: Article
Language:English
Published: Wiley 1992-01-01
Series:Canadian Journal of Infectious Diseases
Online Access:http://dx.doi.org/10.1155/1992/875050
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832566172886761472
author Michel Denis
Marie Bédard
Jacques Gagnon
Yvon Cormier
Michel Laviolette
author_facet Michel Denis
Marie Bédard
Jacques Gagnon
Yvon Cormier
Michel Laviolette
author_sort Michel Denis
collection DOAJ
description C57BL/6 inbred strain mice were instilled intranasally with 150 μg/day of the actinomycete Faeni rectivirgula three days a week as a model of farmer's lung disease. Instilled mice developed a strong alveolitis manifested by a large increase in the number of cells in the bronchoalveolar lavage (BAL) (4.1 x 104 cells in saline controls versus 5.28x 105 cells in F rectivirgula-instilled mice). This influx was associated with a substantial release of pro-inflanm1atory cytokine in the BAL; 170 U/mL of interleukin (IL)-1 in instilled mice whereas saline instilled mice had undetectable levels of cytokines in the BAL. In addition, pulmonary fibrosis was evident in challenged mice at three weeks (twofold increase in lung hydroxyproline levels). Infusion of a rabbit antimouse tumour necrosis factor-alpha was associated with an almost complete abrogation of all markers of the disease. Also, administration of cyclosporine A (50 mg/kg/day) partially prevented the alveolitis (P<0.01) and totally prevented cytokine release and lung fibrosis in challenged mice. These findings underscore the tmmunological basis of hypersensitivity pneumonitis, and suggest that antagonism of inflammatory cytokines may hold promise in the treatment of this pathology.
format Article
id doaj-art-f5f4e68335ef46d19229faffe571b0b9
institution Kabale University
issn 1180-2332
language English
publishDate 1992-01-01
publisher Wiley
record_format Article
series Canadian Journal of Infectious Diseases
spelling doaj-art-f5f4e68335ef46d19229faffe571b0b92025-02-03T01:04:54ZengWileyCanadian Journal of Infectious Diseases1180-23321992-01-013Suppl B11111410.1155/1992/875050Involvement of Cytokines in the Pathogenesis of Hypersensitivity Pneumonitis: Evaluation of Immunotherapeutic Measures in a Mouse ModelMichel DenisMarie BédardJacques GagnonYvon CormierMichel LavioletteC57BL/6 inbred strain mice were instilled intranasally with 150 μg/day of the actinomycete Faeni rectivirgula three days a week as a model of farmer's lung disease. Instilled mice developed a strong alveolitis manifested by a large increase in the number of cells in the bronchoalveolar lavage (BAL) (4.1 x 104 cells in saline controls versus 5.28x 105 cells in F rectivirgula-instilled mice). This influx was associated with a substantial release of pro-inflanm1atory cytokine in the BAL; 170 U/mL of interleukin (IL)-1 in instilled mice whereas saline instilled mice had undetectable levels of cytokines in the BAL. In addition, pulmonary fibrosis was evident in challenged mice at three weeks (twofold increase in lung hydroxyproline levels). Infusion of a rabbit antimouse tumour necrosis factor-alpha was associated with an almost complete abrogation of all markers of the disease. Also, administration of cyclosporine A (50 mg/kg/day) partially prevented the alveolitis (P<0.01) and totally prevented cytokine release and lung fibrosis in challenged mice. These findings underscore the tmmunological basis of hypersensitivity pneumonitis, and suggest that antagonism of inflammatory cytokines may hold promise in the treatment of this pathology.http://dx.doi.org/10.1155/1992/875050
spellingShingle Michel Denis
Marie Bédard
Jacques Gagnon
Yvon Cormier
Michel Laviolette
Involvement of Cytokines in the Pathogenesis of Hypersensitivity Pneumonitis: Evaluation of Immunotherapeutic Measures in a Mouse Model
Canadian Journal of Infectious Diseases
title Involvement of Cytokines in the Pathogenesis of Hypersensitivity Pneumonitis: Evaluation of Immunotherapeutic Measures in a Mouse Model
title_full Involvement of Cytokines in the Pathogenesis of Hypersensitivity Pneumonitis: Evaluation of Immunotherapeutic Measures in a Mouse Model
title_fullStr Involvement of Cytokines in the Pathogenesis of Hypersensitivity Pneumonitis: Evaluation of Immunotherapeutic Measures in a Mouse Model
title_full_unstemmed Involvement of Cytokines in the Pathogenesis of Hypersensitivity Pneumonitis: Evaluation of Immunotherapeutic Measures in a Mouse Model
title_short Involvement of Cytokines in the Pathogenesis of Hypersensitivity Pneumonitis: Evaluation of Immunotherapeutic Measures in a Mouse Model
title_sort involvement of cytokines in the pathogenesis of hypersensitivity pneumonitis evaluation of immunotherapeutic measures in a mouse model
url http://dx.doi.org/10.1155/1992/875050
work_keys_str_mv AT micheldenis involvementofcytokinesinthepathogenesisofhypersensitivitypneumonitisevaluationofimmunotherapeuticmeasuresinamousemodel
AT mariebedard involvementofcytokinesinthepathogenesisofhypersensitivitypneumonitisevaluationofimmunotherapeuticmeasuresinamousemodel
AT jacquesgagnon involvementofcytokinesinthepathogenesisofhypersensitivitypneumonitisevaluationofimmunotherapeuticmeasuresinamousemodel
AT yvoncormier involvementofcytokinesinthepathogenesisofhypersensitivitypneumonitisevaluationofimmunotherapeuticmeasuresinamousemodel
AT michellaviolette involvementofcytokinesinthepathogenesisofhypersensitivitypneumonitisevaluationofimmunotherapeuticmeasuresinamousemodel