LAUSR

The immunosuppressive tumor microenvironment (TME) in glioblastoma (GBM) is mainly driven by tumor‐associated macrophages (TAMs). We explored whether their sustained iron metabolism and immunosuppressive activity were correlated, and whether blocking the central enzyme of the heme catabolism pathway, heme oxygenase‐1 (HO‐1), could reverse their tolerogenic activity. To this end, we investigated iron metabolism in bone marrow‐derived macrophages (BMDMs) isolated from GBM specimens and in in vitro‐derived macrophages (Mφ) from healthy donor (HD) blood monocytes. We found that HO‐1 inhibition abrogated the immunosuppressive activity of both BMDMs and Mφ, and that immunosuppression requires both cell‐to‐cell contact and soluble factors, as HO‐1 inhibition abolished IL‐10 release, and significantly reduced STAT3 activation as well as PD‐L1 expression. Interestingly, not only did HO‐1 inhibition downregulate IDO1 and ARG‐2 gene expression, but also reduced IDO1 enzymatic activity. Moreover, T cell activation status affected PD‐L1 expression and IDO1 activity, which were upregulated in the presence of activated, but not resting, T cells. Our results highlight the crucial role of HO‐1 in the immunosuppressive activity of macrophages in the GBM TME and demonstrate the feasibility of reprogramming them as an alternative therapeutic strategy for restoring immune surveillance.