AI Article Synopsis

  • Glioblastoma (GBM) is a highly aggressive brain tumor challenging to treat due to the blood-brain barrier and the tumor's immunosuppressive environment.
  • A novel immunotherapy strategy using a nanomaterial called BM@MnP-BSA-aPD-1 has been developed, which effectively crosses the blood-brain barrier and targets the tumor microenvironment.
  • This approach enhances anti-tumor immunity through various mechanisms, including activating specific immune pathways and inhibiting immune evasion signals, showing promise for clinical use in GBM treatment.

Article Abstract

Glioblastoma (GBM) is a lethal brain tumor with high levels of malignancy. Most chemotherapy agents show serious systemic cytotoxicity and restricted delivery effectiveness due to the impediments of the blood-brain barrier (BBB). Immunotherapy has developed great potential for aggressive tumor treatments. Disappointingly, its efficacy against GBM is hindered by the immunosuppressive tumor microenvironment (TME) and BBB. Herein, a multiple synergistic immunotherapeutic strategy against GBM was developed based on the nanomaterial-biology interaction. We have demonstrated that this BM@MnP-BSA-aPD-1 can transverse the BBB and target the TME, resulting in amplified synergetic effects of metalloimmunotherapy and photothermal immunotherapy (PTT). The journey of this nanoformulation within the TME contributed to the activation of the stimulator of the interferon gene pathway, the initiation of the immunogenic cell death effect, and the inhibition of the programmed cell death-1/programmed cell death ligand 1 (PD-1/PD-L1) signaling axis. This nanomedicine revitalizes the immunosuppressive TME and evokes the cascade effect of antitumor immunity. Therefore, the combination of BM@MnP-BSA-aPD-1 and PTT without chemotherapeutics presents favorable benefits in anti-GBM immunotherapy and exhibits immense potential for clinical translational applications.

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Source
http://dx.doi.org/10.1021/acsnano.4c01253DOI Listing

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