KAIST Uncovers the “Hidden Key” to Immunotherapy for Intractable Brain Tumors (IMAGE)
Caption
Figure 2. Anti-CTLA-4–induced B-cell immune responses in tumor-draining lymph nodes and antitumor immune responses within brain tumors in mouse glioma models
(A) Comparison of survival and brain tumor burden between wild-type and B-cell-deficient mice following anti-CTLA-4 treatment
(B) Analysis of changes in B cells, germinal center B cells, and T follicular helper cells in tumor-draining lymph nodes following anti-CTLA-4 treatment
(C) Analysis of immunoglobulin G (IgG) distribution in brain tumor tissue and of IgG-bound glioma cells following anti-CTLA-4 treatment
(D) Establishment of an mCherry-EGFP dual-reporter glioma model and analysis of tumor cell phagocytosis by intratumoral phagocytes following anti-CTLA-4 treatment
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