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Metabolic dysregulation and immune suppression are intrinsically linked within the solid tumor microenvironment, yet effective strategies to simultaneously reprogram tumor metabolism and restore antitumor immunity remain challenging. Here, we present a tumor-tropic bacterial–nanoparticle hybrid (SW@CDFM) that integrates metabolic reprogramming with immune activation for synergistic cancer treatment. The designed biohybrid system is constructed by covalently conjugating Shewanella oneidensis bacteria with tumor cell membrane-camouflaged DOX-Fe/CpG nanoparticles. Leveraging the intrinsic hypoxia tropism of Shewanella, SW@CDFM selectively accumulates in tumors, alleviates lactate-driven acidosis, and remodels the metabolic landscape of the tumor microenvironment. Concurrently, pH-responsive release of doxorubicin and CpG induces immunogenic cell death and activates dendritic cells, initiating a coordinated innate-to-adaptive immune cascade characterized by macrophage repolarization and robust cytotoxic T-cell infiltration. When combined with αPD-1 checkpoint blockade, SW@CDFM achieves more than 90% tumor growth inhibition in murine models and effectively converts immunologically “cold” tumors into “hot” ones. This work establishes a paradigm for the rational design of biohybrid systems that synergize microbial therapy with nanotechnology to surmount biological barriers in cancer treatment.
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Ji et al. (2026) studied this question.
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