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Stimulation of tumoricidal immunity via bacteriotherapy inhibits glioblastoma relapse. | LitMetric

AI Article Synopsis

  • Glioblastoma multiforme (GBM) is a highly aggressive brain tumor that poses significant treatment challenges due to its invasive nature and compromised immune response, leading to treatment failures and tumor recurrence.
  • Researchers developed a novel bacterium-hydrogel superstructure that targets and destroys residual GBM cells, enhancing immune responses to prevent postoperative relapse.
  • The system utilizes engineered Salmonella vehicles combined with nanocapsules to stimulate an immune response and promote the recruitment of immune cells, showing promise for treating patients with GBM at high risk of recurrence.

Article Abstract

Glioblastoma multiforme (GBM) is a highly aggressive brain tumor characterized by invasive behavior and a compromised immune response, presenting treatment challenges. Surgical debulking of GBM fails to address its highly infiltrative nature, leaving neoplastic satellites in an environment characterized by impaired immune surveillance, ultimately paving the way for tumor recurrence. Tracking and eradicating residual GBM cells by boosting antitumor immunity is critical for preventing postoperative relapse, but effective immunotherapeutic strategies remain elusive. Here, we report a cavity-injectable bacterium-hydrogel superstructure that targets GBM satellites around the cavity, triggers GBM pyroptosis, and initiates innate and adaptive immune responses, which prevent postoperative GBM relapse in male mice. The immunostimulatory Salmonella delivery vehicles (SDVs) engineered from attenuated Salmonella typhimurium (VNP20009) seek and attack GBM cells. Salmonella lysis-inducing nanocapsules (SLINs), designed to trigger autolysis, are tethered to the SDVs, eliciting antitumor immune response through the intracellular release of bacterial components. Furthermore, SDVs and SLINs administration via intracavitary injection of the ATP-responsive hydrogel can recruit phagocytes and promote antigen presentation, initiating an adaptive immune response. Therefore, our work offers a local bacteriotherapy for stimulating anti-GBM immunity, with potential applicability for patients facing malignancies at a high risk of recurrence.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11102507PMC
http://dx.doi.org/10.1038/s41467-024-48606-5DOI Listing

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