A role for MCP-1/CCR2 in interstitial lung disease in children

<p>Abstract</p> <p>Background</p> <p>Interstitial lung diseases (ILD) are chronic inflammatory disorders leading to pulmonary fibrosis. Monocyte chemotactic protein 1 (MCP-1) promotes collagen synthesis and deletion of the MCP-1 receptor CCR2 protects from pulmonary fib...

Full description

Bibliographic Details
Main Authors: Reinhardt Dietrich, Prell Christine, Zissel Gernot, Nicolai Thomas, Griese Matthias, Hartl Dominik, Schendel Dolores J, Krauss-Etschmann Susanne
Format: Article
Language:English
Published: BMC 2005-08-01
Series:Respiratory Research
Subjects:
Online Access:http://respiratory-research.com/content/6/1/93
_version_ 1818021045614936064
author Reinhardt Dietrich
Prell Christine
Zissel Gernot
Nicolai Thomas
Griese Matthias
Hartl Dominik
Schendel Dolores J
Krauss-Etschmann Susanne
author_facet Reinhardt Dietrich
Prell Christine
Zissel Gernot
Nicolai Thomas
Griese Matthias
Hartl Dominik
Schendel Dolores J
Krauss-Etschmann Susanne
author_sort Reinhardt Dietrich
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>Interstitial lung diseases (ILD) are chronic inflammatory disorders leading to pulmonary fibrosis. Monocyte chemotactic protein 1 (MCP-1) promotes collagen synthesis and deletion of the MCP-1 receptor CCR2 protects from pulmonary fibrosis in ILD mouse models. We hypothesized that pulmonary MCP-1 and CCR2<sup>+ </sup>T cells accumulate in pediatric ILD and are related to disease severity.</p> <p>Methods</p> <p>Bronchoalveolar lavage fluid was obtained from 25 children with ILD and 10 healthy children. Levels of pulmonary MCP-1 and Th1/Th2-associated cytokines were quantified at the protein and the mRNA levels. Pulmonary CCR2<sup>+</sup>, CCR4<sup>+</sup>, CCR3<sup>+</sup>, CCR5<sup>+ </sup>and CXCR3<sup>+ </sup>T cells were quantified by flow-cytometry.</p> <p>Results</p> <p>CCR2<sup>+ </sup>T cells and MCP-1 levels were significantly elevated in children with ILD and correlated with forced vital capacity, total lung capacity and ILD disease severity scores. Children with lung fibrosis had significantly higher MCP-1 levels and CCR2<sup>+ </sup>T cells in bronchoalveolar lavage fluid compared to non-fibrotic children.</p> <p>Conclusion</p> <p>The results indicate that pulmonary CCR2<sup>+ </sup>T cells and MCP-1 contribute to the pathogenesis of pediatric ILD and might provide a novel target for therapeutic strategies.</p>
first_indexed 2024-04-14T08:13:38Z
format Article
id doaj.art-3c74eecf73284bc19ac4ba97460fd3f6
institution Directory Open Access Journal
issn 1465-9921
language English
last_indexed 2024-04-14T08:13:38Z
publishDate 2005-08-01
publisher BMC
record_format Article
series Respiratory Research
spelling doaj.art-3c74eecf73284bc19ac4ba97460fd3f62022-12-22T02:04:28ZengBMCRespiratory Research1465-99212005-08-01619310.1186/1465-9921-6-93A role for MCP-1/CCR2 in interstitial lung disease in childrenReinhardt DietrichPrell ChristineZissel GernotNicolai ThomasGriese MatthiasHartl DominikSchendel Dolores JKrauss-Etschmann Susanne<p>Abstract</p> <p>Background</p> <p>Interstitial lung diseases (ILD) are chronic inflammatory disorders leading to pulmonary fibrosis. Monocyte chemotactic protein 1 (MCP-1) promotes collagen synthesis and deletion of the MCP-1 receptor CCR2 protects from pulmonary fibrosis in ILD mouse models. We hypothesized that pulmonary MCP-1 and CCR2<sup>+ </sup>T cells accumulate in pediatric ILD and are related to disease severity.</p> <p>Methods</p> <p>Bronchoalveolar lavage fluid was obtained from 25 children with ILD and 10 healthy children. Levels of pulmonary MCP-1 and Th1/Th2-associated cytokines were quantified at the protein and the mRNA levels. Pulmonary CCR2<sup>+</sup>, CCR4<sup>+</sup>, CCR3<sup>+</sup>, CCR5<sup>+ </sup>and CXCR3<sup>+ </sup>T cells were quantified by flow-cytometry.</p> <p>Results</p> <p>CCR2<sup>+ </sup>T cells and MCP-1 levels were significantly elevated in children with ILD and correlated with forced vital capacity, total lung capacity and ILD disease severity scores. Children with lung fibrosis had significantly higher MCP-1 levels and CCR2<sup>+ </sup>T cells in bronchoalveolar lavage fluid compared to non-fibrotic children.</p> <p>Conclusion</p> <p>The results indicate that pulmonary CCR2<sup>+ </sup>T cells and MCP-1 contribute to the pathogenesis of pediatric ILD and might provide a novel target for therapeutic strategies.</p>http://respiratory-research.com/content/6/1/93ChemokinesMCP-1CCR2Bronchoalveolar LavageChildrenInterstitial Lung Diseases
spellingShingle Reinhardt Dietrich
Prell Christine
Zissel Gernot
Nicolai Thomas
Griese Matthias
Hartl Dominik
Schendel Dolores J
Krauss-Etschmann Susanne
A role for MCP-1/CCR2 in interstitial lung disease in children
Respiratory Research
Chemokines
MCP-1
CCR2
Bronchoalveolar Lavage
Children
Interstitial Lung Diseases
title A role for MCP-1/CCR2 in interstitial lung disease in children
title_full A role for MCP-1/CCR2 in interstitial lung disease in children
title_fullStr A role for MCP-1/CCR2 in interstitial lung disease in children
title_full_unstemmed A role for MCP-1/CCR2 in interstitial lung disease in children
title_short A role for MCP-1/CCR2 in interstitial lung disease in children
title_sort role for mcp 1 ccr2 in interstitial lung disease in children
topic Chemokines
MCP-1
CCR2
Bronchoalveolar Lavage
Children
Interstitial Lung Diseases
url http://respiratory-research.com/content/6/1/93
work_keys_str_mv AT reinhardtdietrich aroleformcp1ccr2ininterstitiallungdiseaseinchildren
AT prellchristine aroleformcp1ccr2ininterstitiallungdiseaseinchildren
AT zisselgernot aroleformcp1ccr2ininterstitiallungdiseaseinchildren
AT nicolaithomas aroleformcp1ccr2ininterstitiallungdiseaseinchildren
AT griesematthias aroleformcp1ccr2ininterstitiallungdiseaseinchildren
AT hartldominik aroleformcp1ccr2ininterstitiallungdiseaseinchildren
AT schendeldoloresj aroleformcp1ccr2ininterstitiallungdiseaseinchildren
AT kraussetschmannsusanne aroleformcp1ccr2ininterstitiallungdiseaseinchildren
AT reinhardtdietrich roleformcp1ccr2ininterstitiallungdiseaseinchildren
AT prellchristine roleformcp1ccr2ininterstitiallungdiseaseinchildren
AT zisselgernot roleformcp1ccr2ininterstitiallungdiseaseinchildren
AT nicolaithomas roleformcp1ccr2ininterstitiallungdiseaseinchildren
AT griesematthias roleformcp1ccr2ininterstitiallungdiseaseinchildren
AT hartldominik roleformcp1ccr2ininterstitiallungdiseaseinchildren
AT schendeldoloresj roleformcp1ccr2ininterstitiallungdiseaseinchildren
AT kraussetschmannsusanne roleformcp1ccr2ininterstitiallungdiseaseinchildren