Demonstrates reduced tumor recurrence and effective infection prevention in a post-surgical model, suggesting a new treatment approach.
), while the hydrogel exhibited potent antibacterial activity against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus). In vivo evaluation using a post-tumor-resection mouse model confirmed that Gel@CAR-M@Mn@ELE significantly suppressed tumor recurrence and prolonged survival. The combination of bioactive components within the hydrogel modulated the immunosuppressive tumor microenvironment, thereby enhancing its immunotherapeutic efficacy. Additionally, in a bacterial wound infection model, the hydrogel effectively inhibited bacterial growth and accelerated wound healing. The Gel@CAR-M@Mn@ELE offers a novel and promising strategy, supported by experimental evidence, for concurrently addressing the critical post-surgical challenges of tumor recurrence and wound infection.
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Qin et al. (2026) studied this question.
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