4.7 Article

Kunitz-type protease inhibitor TFPI2 remodels stemness and immunosuppressive tumor microenvironment in glioblastoma

Journal

NATURE IMMUNOLOGY
Volume 24, Issue 10, Pages 1654-+

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41590-023-01605-y

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TFPI2 promotes glioblastoma stem cell self-renewal and connects stemness to microglia immunosuppression. Targeting TFPI2-mediated glioblastoma stem cell-microglia symbiosis inhibits tumor growth and synergizes with anti-PD1 therapy in glioblastoma.
Glioblastoma (GBM) tumors consist of multiple cell populations, including self-renewing glioblastoma stem cells (GSCs) and immunosuppressive microglia. Here we identified Kunitz-type protease inhibitor TFPI2 as a critical factor connecting these cell populations and their associated GBM hallmarks of stemness and immunosuppression. TFPI2 promotes GSC self-renewal and tumor growth via activation of the c-Jun N-terminal kinase-signal transducer and activator of transcription (STAT)3 pathway. Secreted TFPI2 interacts with its functional receptor CD51 on microglia to trigger the infiltration and immunosuppressive polarization of microglia through activation of STAT6 signaling. Inhibition of the TFPI2-CD51-STAT6 signaling axis activates T cells and synergizes with anti-PD1 therapy in GBM mouse models. In human GBM, TFPI2 correlates positively with stemness, microglia abundance, immunosuppression and poor prognosis. Our study identifies a function for TFPI2 and supports therapeutic targeting of TFPI2 as an effective strategy for GBM. Here the authors show that TFPI2 promotes glioblastoma stem cell self-renewal and connects stemness to microglia immunosuppression, plus targeting TFPI2-mediated glioblastoma stem cell-microglia symbiosis inhibits tumor growth and synergizes with anti-PD1 therapy in glioblastoma.

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