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Dual threat: VSIG4⁺ macrophages use IL-11 and VSIG4 to silence T cells
Darya Khantakova1, Marco Colonna1
1Department of Pathology and Immunology, Washington University in St. Louis School of Medicine, St. Louis, MO, USA.
Abstract:
In this issue of Developmental Cell, Ma et al. show that embryonically derived VSIG4⁺ macrophages suppress CD8⁺ T cell responses across cancers. They identify IL-11 as a key effector and MEF2C as a transcriptional regulator of VSIG4⁺ macrophages, highlighting new therapeutic avenues for targeting immunosuppressive tumor-associated macrophages to improve immunotherapy outcomes.
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