» Articles » PMID: 30414858

Innate Immune Crosstalk in Asthmatic Airways: Innate Lymphoid Cells Coordinate Polarization of Lung Macrophages

Overview
Date 2018 Nov 12
PMID 30414858
Citations 42
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Recent studies have emphasized the role of innate lymphoid cells (ILCs) in the development of asthma. The involvement of group 2 innate lymphoid cells (ILC2s) in asthma is well studied: however, the participation of other types of ILCs in the development of asthma remains unclear.

Objective: This study aims to understand the role of various ILCs in patients with asthma, especially their effect on macrophage polarization.

Methods: Each subset of ILCs and macrophages in induced sputum from 51 steroid-naive patients with asthma and 18 healthy donors was analyzed by using flow cytometry. Alveolar macrophages (AM) were sorted and cocultured with each subset of ILCs to determine whether the polarization of macrophages could be regulated by ILCs.

Results: In addition to ILC2s, numbers of group 1 innate lymphoid cells (ILC1s) and group 3 innate lymphoid cells (ILC3s) were increased in induced sputum from asthmatic patients when compared with those in healthy control subjects. The dominance of macrophages in induced sputum was more prominent in asthmatic patients than in healthy control subjects. A positive correlation between numbers of ILC2s and numbers of M2 macrophages and those of ILC1s/ILC3s and M1 macrophages was observed. Coculture of ILC2s with AMs induced expression of M2 macrophage-related genes, whereas coculture of ILC1s and ILC3s with AMs induced expression of M1 macrophage-related genes through cytokine secretion, as well as cell-cell contact. According to the inflammatory signature, patients with eosinophilic asthma have more ILC2s and M2 macrophages, and those with noneosinophilic asthma have an M1 macrophage-dominant profile.

Conclusion: A different subset of ILCs regulates macrophage polarization, contributing to developing the distinct phenotype of asthma.

Citing Articles

Chronic Inflammation in Asthma: Looking Beyond the Th2 Cell.

Olsthoorn S, van Krimpen A, Hendriks R, Stadhouders R Immunol Rev. 2025; 330(1):e70010.

PMID: 40016948 PMC: 11868696. DOI: 10.1111/imr.70010.


Peroxisome Metabolism Pathway and EHHADH Expression are Downregulated in Macrophages in Neutrophilic Asthma.

Chen G, Gu W, Huang C, Kong W, Zhao L, Jie H Allergy Asthma Immunol Res. 2025; 17(1):111-126.

PMID: 39895606 PMC: 11791367. DOI: 10.4168/aair.2025.17.1.111.


Contribution of IL-17C-mediated macrophage polarization to Type 17 inflammation in neutrophilic asthma.

Wen Y, Chen Q, Wang H, Xie S, Chen H, Yao W Cell Commun Signal. 2024; 22(1):557.

PMID: 39568050 PMC: 11580697. DOI: 10.1186/s12964-024-01937-8.


Therapeutic efficacy of thrombin-preconditioned mesenchymal stromal cell-derived extracellular vesicles on Escherichia coli-induced acute lung injury in mice.

Bang Y, Hwang S, Kim Y, Sung D, Yang M, Ahn S Respir Res. 2024; 25(1):303.

PMID: 39112999 PMC: 11308396. DOI: 10.1186/s12931-024-02908-w.


Innate Type-2 Cytokines: From Immune Regulation to Therapeutic Targets.

Kim H, Jeong D, Kim J, Chung D Immune Netw. 2024; 24(1):e6.

PMID: 38455467 PMC: 10917574. DOI: 10.4110/in.2024.24.e6.