<p>a Sing-cell RNA sequencing data was clustered and annotated using Azimuth cell annotation methods. b The cells were re-clustered into subpopulations. c Each cluster was verified using the top marker genes. d The clusters were separated into treatment groups. e Enhanced volcano plot showing enriched cluster genes using DEG analysis. f Dittobar plot showing the different proportions of subsets in the groups. g Re-clustering of the T-cell clusters. h Re-clustering of macrophage clusters. DEG, differentially expressed genes</p>