Expansion of Disease Specific Cardiac Macrophages in Immune Checkpoint Inhibitor Myocarditis

Abstract

AbstractBackgroundImmune checkpoint inhibitors (ICIs), antibodies targeting PD-1/PD-L1 or CTLA4 have revolutionized cancer management but are associated with devastating immune-related adverse events (irAEs) including myocarditis. The main risk factor for ICI myocarditis is the use of combination PD-1 and CTLA4 inhibition. ICI-myocarditis is often fulminant and is pathologically characterized by myocardial infiltration of T lymphocytes and macrophages. While much has been learned regarding the role of T-cells in ICI-myocarditis, little is understood regarding the identity, transcriptional diversity, and functions of infiltrating macrophages.MethodsWe employed an established murine ICI myocarditis model (Ctla4+/-Pdcd1-/-mice) to explore the cardiac immune landscape using single-cell RNA-sequencing, immunostaining, flow cytometry, in situ RNA hybridization and molecular imaging and antibody neutralization studies.ResultsWe observed marked increases in CCR2+monocyte-derived macrophages and CD8+T-cells in this model. The macrophage compartment was heterogeneous and displayed marked enrichment in an inflammatory CCR2+subpopulation highly expressingCxcl9,Cxcl10,Gbp2b, andFcgr4that originated from CCR2+monocytes. Importantly, a similar macrophage population expressingCXCL9,CXCL10, and CD16α (human homologue of mouse FcgR4) was found selectively expanded in patients with ICI myocarditis compared to other forms of heart failure and myocarditis.In silicoprediction of cell-cell communication suggested interactions between T-cells andCxcl9+Cxcl10+macrophages via IFN-γ and CXCR3 signaling pathways. Depleting CD8+T-cells, macrophages, and blockade of IFN-γ signaling blunted the expansion ofCxcl9+Cxcl10+macrophages in the heart and attenuated myocarditis suggesting that this interaction was necessary for disease pathogenesis.ConclusionThese data demonstrate that ICI-myocarditis is associated with the expansion of a specific population of IFN-γ induced inflammatory macrophages and suggest the possibility that IFN-γ blockade may be considered as a treatment option for this devastating condition.