Highlight
- Post-CD7 CAR-T therapy lymphoproliferative disorder (PCLD) is characterized by CD7-negative dysfunctional T cells and emergence of EBV-positive B cell proliferation.
- Spatial multi-omics identify immunosuppressive macrophage populations expressing IDO1 that form niches limiting effective T-cell infiltration in PCLD.
- EBV-driven B cells in PCLD acquire plasmacytic features with ongoing proliferation, remodeling the local microenvironment favoring malignant transformation.
- The study elucidates mechanisms underpinning EBV reactivation and lymphoproliferation after CD7 CAR-T, suggesting therapeutic avenues targeting macrophage suppression and inhibitory pathways.
Study Background
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