Table 1.
Recent advances of nanozyme-based enhanced cancer immunotherapy
Nanozyme | Catalytic activity | Synergistic therapy | Therapeutic effects | References |
---|---|---|---|---|
Hyaluronic- and polyethylene glycol-decorated Cu-based nanozymes | POD-like activity | Photothermal therapy (PTT) | Induction of immunogenic death (ICD) to boost the immunological function of effector CAR-T cells | [51] |
Glucose oxidase (GOx), hemin, dihydroartemisinic (DHA) enveloped in ZIF-8 framework | GOx activity, POD-like activity | Anti-PD-L1 | Formation of elevated ROS to cause tumor cell death, to release TAAs, to enhance infiltration of tumor-specific T cells into tumor site | [52] |
Core–shell gold nanocage@manganese dioxide (AuNC@MnO2) nanozyme | CAT-like activity, NIR-mediated conversion of O2 to .O2− | Photodynamic therapy (PDT) | Induction of ICD, release of damage-associated molecular patterns (DAMPs), activation of effector T cells | [53] |
Phospholipid-coated Na2S2O8 nanoparticles | Generation of sulfate (.SO4−) and hydroxyl (OH.) radical by dissociation of persulfate | Anti-CTLA-4 | High ROS level to induce ICD, release of DAMPs, activation of tumor-specific T cells | [55] |
Co-loading of Ce6 and DOX into hollow manganese dioxide (H-MnO2) | CAT-like activity | PDT, chemotherapy, anti-PD-L1 | O2 supplement for relief of tumor hypoxia, M2 macrophage polarization, induction of ICD, cytotoxic T lymphocyte CTL) activation | [61] |
Combination of CaO2- and MnO2-based nanozymes | H2O2-generating activity, CAT-like activity, | Anti-CTLA-4, chemotherapy | Relief of tumor hypoxia, suppression of Treg activity, activation of CTLs | [63] |
Iron- and manganese-based nanozymes encapsuled into mesoporous silica nanoparticles (MSN) | CAT- and POD-like activity | Delivery of TGF-β inhibitor | Relief of tumor hypoxia, M2 macrophage polarization, suppression of Tregs, induction of ICD, activation of effector T cells | [62] |