KAIST Uncovers the “Hidden Key” to Immunotherapy for Intractable Brain Tumors (IMAGE)
Caption
Figure 1. Proposed model. In glioma-bearing mice, anti-CTLA-4 treatment increases inducible T cell costimulator (ICOS) expression on CD4 T cells and expands T follicular helper (TFH) cells in tumor-draining dcLNs. Enhanced TFH responses promote the expansion of germinal center (GC) B cells, leading to clonal expansion and class switching. This induces glioma-reactive IgG production, which binds glioma cells and enhances phagocytosis by tumor-infiltrating myeloid cells, contributing to glioma control. Graphics created with BioRender
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KAIST
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