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Crosstalk between macrophages and innate lymphoid cells (ILCs) in diseases.

Authors :
Yin, Guoquan
Zhao, Chen
Pei, Weiya
Source :
International Immunopharmacology. Sep2022, Vol. 110, pN.PAG-N.PAG. 1p.
Publication Year :
2022

Abstract

• ILCs play complex and diverse roles in macrophages development, homeostasis, polarization, inflammation, or viral infection. • ILCs regulate a wider range of immune responses through functional interactions with macrophages. They work together to coordinate the immune response of the organs of the whole body to control tissue homeostasis or cause immune disorders. Innate lymphoid cells (ILCs) and macrophages are tissue-resident cells that play important roles in tissue-immune homeostasis and immune regulation. ILCs are mainly distributed on the barrier surfaces of mammals to ensure immunity or tissue homeostasis following host, microbial, or environmental stimulation. Their complex relationships with different organs enable them to respond quickly to disturbances in environmental conditions and organ homeostasis, such as during infections and tissue damage. Gradually emerging evidence suggests that ILCs also play complex and diverse roles in macrophage development, homeostasis, polarization, inflammation, and viral infection. In turn, macrophages also determine the fate of ILCs to some extent, which indicates that network crossover between these interactions is a key determinant of the immune response. More work is needed to better define the crosstalk of ILCs with macrophages in different tissues and demonstrate how it is affected during inflammation and other diseases. Here, we summarize current research on the functional interactions between ILCs and macrophages and consider the potential therapeutic utility of these interactions for the benefit of human health. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15675769
Volume :
110
Database :
Academic Search Index
Journal :
International Immunopharmacology
Publication Type :
Academic Journal
Accession number :
158443539
Full Text :
https://doi.org/10.1016/j.intimp.2022.108937