Crosstalk between CD64+MHCII+ macrophages and CD4+ T cells drives joint pathology during chikungunya
Fok‐Moon Lum, Yi‐Hao Chan, Teck‐Hui Teo, Étienne Becht, Siti Naqiah Amrun, Karen Ww Teng, Siddesh V. Hartimath, Nicholas Kim‐Wah Yeo, Wearn‐Xin Yee, Nicholas Ang, Anthony M Torres-Ruesta, Siew‐Wai Fong, Julian Goggi, Evan W. Newell, Laurent Rénia, Guillaume Carissimo, Lisa F. P. Ng
Abstract
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.