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CD5L attenuates allergic airway inflammation by expanding CD11c high alveolar macrophages and inhibiting NLRP3 inflammasome activation via HDAC2.

Authors :
Weng D
Gao S
Shen H
Yao S
Huang Q
Zhang Y
Huang W
Wang Y
Zhang X
Yin Y
Xu W
Source :
Immunology [Immunology] 2022 Nov; Vol. 167 (3), pp. 384-397. Date of Electronic Publication: 2022 Jul 26.
Publication Year :
2022

Abstract

Allergic asthma is an airway inflammatory disease dominated by type 2 immune responses and there is currently no curative therapy for asthma. CD5-like antigen (CD5L) has been known to be involved in a variety of inflammatory diseases. However, the role of CD5L in allergic asthma remains unclear. In the present study, mice were treated with recombinant CD5L (rCD5L) during house dust mite (HDM) and ovalbumin (OVA) challenge to determine the role of CD5L in allergic asthma, and the underlying mechanism was further explored. Compared with PBS group, serum CD5L levels of asthmatic mice were significantly decreased, and the levels of CD5L in lung tissues and bronchoalveolar lavage fluid (BALF) were significantly increased. CD5L reduced airway inflammation and Th2 immune responses in asthmatic mice. CD5L exerted its anti-inflammatory function by increasing CD11c <superscript>high</superscript> alveolar macrophages (CD11c <superscript>high</superscript> AMs), and the anti-inflammatory role of CD11c <superscript>high</superscript> AMs in allergic asthma was confirmed by CD11c <superscript>high</superscript> AMs depletion and transfer assays. In addition, CD5L increased the CD5L <superscript>+</superscript> macrophages and inhibited NLRP3 inflammasome activation by increasing HDAC2 expression in lung tissues of asthmatic mice. Hence, our study implicates that CD5L has potential usefulness for asthma treatment.<br /> (© 2022 The Authors. Immunology published by John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1365-2567
Volume :
167
Issue :
3
Database :
MEDLINE
Journal :
Immunology
Publication Type :
Academic Journal
Accession number :
35794812
Full Text :
https://doi.org/10.1111/imm.13543