» Articles » PMID: 14523040

Anti-IL-5 Treatment Reduces Deposition of ECM Proteins in the Bronchial Subepithelial Basement Membrane of Mild Atopic Asthmatics

Overview
Journal J Clin Invest
Specialty General Medicine
Date 2003 Oct 3
PMID 14523040
Citations 259
Authors
Affiliations
Soon will be listed here.
Abstract

Eosinophil-derived TGF-beta has been implicated in remodeling events in asthma. We hypothesized that reduction of bronchial mucosal eosinophils with anti-IL-5 would reduce markers of airway remodeling. Bronchial biopsies were obtained before and after three infusions of a humanized, anti-IL-5 monoclonal antibody (mepolizumab) in 24 atopic asthmatics in a randomized, double-blind, placebo-controlled study. The thickness and density of tenascin, lumican, and procollagen III in the reticular basement membrane (RBM) were quantified immunohistochemically by confocal microscopy. Expression of TGF-beta1 mRNA by airway eosinophils was assessed by in situ hybridization, and TGF-beta1 protein was measured in bronchoalveolar lavage (BAL) fluid by ELISA. At baseline, airway eosinophil infiltration and ECM protein deposition was increased in the RBM of asthmatics compared with nonasthmatic controls. Treating asthmatics with anti-IL-5 antibody, which specifically decreased airway eosinophil numbers, significantly reduced the expression of tenascin, lumican, and procollagen III in the bronchial mucosal RBM when compared with placebo. In addition, anti-IL-5 treatment was associated with a significant reduction in the numbers and percentage of airway eosinophils expressing mRNA for TGF-beta1 and the concentration of TGF-beta1 in BAL fluid. Therefore eosinophils may contribute to tissue remodeling processes in asthma by regulating the deposition of ECM proteins.

Citing Articles

Clinical Evidence of the Use of Mepolizumab in the Treatment of Chronic Rhinosinusitis with Nasal Polyps: A Prospective Observational Study.

Moffa A, Iafrati F, Giorgi L, Nardelli D, Carnuccio L, Baptista P Healthcare (Basel). 2025; 13(4).

PMID: 39997294 PMC: 11855528. DOI: 10.3390/healthcare13040419.


Role of the TGF-β cytokine and its gene polymorphisms in asthma etiopathogenesis.

Plichta J, Panek M Front Allergy. 2025; 6:1529071.

PMID: 39949968 PMC: 11821632. DOI: 10.3389/falgy.2025.1529071.


Time is lung: higher preservation of lung function in severe asthma patients after earlier mepolizumab treatment.

Gonzalez-Barcala F, Bobolea I, Dominguez-Ortega J, Banas-Conejero D, Antelo-Cea E, Martinez-Moragon E ERJ Open Res. 2025; 11(1).

PMID: 39902267 PMC: 11788806. DOI: 10.1183/23120541.00211-2024.


Epithelial-Mesenchymal Transition in Chronic Rhinosinusitis.

Choi T, Ryu S, Bae J, Yoo S, Mo J J Rhinol. 2024; 31(2):67-77.

PMID: 39664411 PMC: 11566545. DOI: 10.18787/jr.2024.00022.


Dual therapy with corticosteroid ablates the beneficial effect of DP2 antagonism in chronic experimental asthma.

Ullah M, Rittchen S, Li J, Curren B, Namubiru P, Ahmed T Nat Commun. 2024; 15(1):10253.

PMID: 39592603 PMC: 11599388. DOI: 10.1038/s41467-024-54670-8.


References
1.
Wilson J, Li X . The measurement of reticular basement membrane and submucosal collagen in the asthmatic airway. Clin Exp Allergy. 1997; 27(4):363-71. View

2.
Hakonarson H, Maskeri N, Carter C, Chuang S, Grunstein M . Autocrine interaction between IL-5 and IL-1beta mediates altered responsiveness of atopic asthmatic sensitized airway smooth muscle. J Clin Invest. 1999; 104(5):657-67. PMC: 408541. DOI: 10.1172/JCI7137. View

3.
Olivieri D, Chetta A, Del Donno M, Bertorelli G, Casalini A, Pesci A . Effect of short-term treatment with low-dose inhaled fluticasone propionate on airway inflammation and remodeling in mild asthma: a placebo-controlled study. Am J Respir Crit Care Med. 1997; 155(6):1864-71. DOI: 10.1164/ajrccm.155.6.9196087. View

4.
Li X, Wilson J . Increased vascularity of the bronchial mucosa in mild asthma. Am J Respir Crit Care Med. 1997; 156(1):229-33. DOI: 10.1164/ajrccm.156.1.9607066. View

5.
Ying S, Meng Q, Zeibecoglou K, Robinson D, Macfarlane A, Humbert M . Eosinophil chemotactic chemokines (eotaxin, eotaxin-2, RANTES, monocyte chemoattractant protein-3 (MCP-3), and MCP-4), and C-C chemokine receptor 3 expression in bronchial biopsies from atopic and nonatopic (Intrinsic) asthmatics. J Immunol. 1999; 163(11):6321-9. View