Spatial and Single Cell Mapping of Human Lymph Node Disease

To determine the cellular and molecular basis of Castleman Disease (CD), we analyze the spatial proteome of spatial proteome and transcriptome of 22 cases of Unicentric CD, idiopathic Multicentric CD, HHV8-associated MCD, and reactive lymph nodes. CD shows increased stromal cells that form unique microenvironments. Interaction of activated follicular dendritic cell (FDC) cytoplasmic meshworks with mantle-zone B cells is associated with B-cell activation and differentiation. CXCL13+ FDCs, PDGFRA+ T-zone reticular cells (TRC), and ACTA2-positive perivascular reticular cells (PRC) were the predominant source of increased VEGF expression and IL-6 signaling. MCD is characterized by increased TRC while UCD shows increased B-reticular cells (BRC). VEGF expression by FDCs is associated with peri-follicular neovascularization. FDC, TRC and PRC of CD activates JAK-STAT, TGFß, and MAPK pathways via specific ligand-receptor interactions. Here, we show that stromal-cell activation and associated B-cell activation and differentiation, neovascularization and stromal remodeling underlie CD. Overall design: Lymph node bioposies were otained from patients diagnosed with Kikuchi-Fujimoto disease, castleman disease, or experiencing an immune reaction. The objective to identify how cell interactions vary between the states was undertaken using multiplexed imaging technologies (PhenoCycler, RNAscope) and single-cell sequencing.