Crosstalk between CD64+MHCII+ macrophages and CD4+ T cells drives joint pathology during chikungunya

Bibliographic Details
Title: Crosstalk between CD64+MHCII+ macrophages and CD4+ T cells drives joint pathology during chikungunya
Authors: Fok-Moon Lum, Yi-Hao Chan, Teck-Hui Teo, Etienne Becht, Siti Naqiah Amrun, Karen WW Teng, Siddesh V Hartimath, Nicholas KW Yeo, Wearn-Xin Yee, Nicholas Ang, Anthony M Torres-Ruesta, Siew-Wai Fong, Julian L Goggi, Evan W Newell, Laurent Renia, Guillaume Carissimo, Lisa FP Ng
Source: EMBO Molecular Medicine, Vol 16, Iss 3, Pp 641-663 (2024)
Publisher Information: Springer Nature, 2024.
Publication Year: 2024
Collection: LCC:Medicine (General)
LCC:Genetics
Subject Terms: Chikungunya, Immune Crosstalk, Immunopathogenesis, GM-CSF, Medicine (General), R5-920, Genetics, QH426-470
More Details: Abstract Communications between immune cells are essential to ensure appropriate coordination of their activities. Here, we observed the infiltration of activated macrophages into the joint-footpads of chikungunya virus (CHIKV)-infected animals. Large numbers of CD64+MHCII+ and CD64+MHCII- macrophages were present in the joint-footpad, preceded by the recruitment of their CD11b+Ly6C+ inflammatory monocyte precursors. Recruitment and differentiation of these myeloid subsets were dependent on CD4+ T cells and GM-CSF. Transcriptomic and gene ontology analyses of CD64+MHCII+ and CD64+MHCII- macrophages revealed 89 differentially expressed genes, including genes involved in T cell proliferation and differentiation pathways. Depletion of phagocytes, including CD64+MHCII+ macrophages, from CHIKV-infected mice reduced disease pathology, demonstrating that these cells play a pro-inflammatory role in CHIKV infection. Together, these results highlight the synergistic dynamics of immune cell crosstalk in driving CHIKV immunopathogenesis. This study provides new insights in the disease mechanism and offers opportunities for development of novel anti-CHIKV therapeutics.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1757-4684
Relation: https://doaj.org/toc/1757-4684
DOI: 10.1038/s44321-024-00028-y
Access URL: https://doaj.org/article/c0fe0f20a551413cb93e952b39752db9
Accession Number: edsdoj.0fe0f20a551413cb93e952b39752db9
Database: Directory of Open Access Journals
More Details
ISSN:17574684
DOI:10.1038/s44321-024-00028-y
Published in:EMBO Molecular Medicine
Language:English