Table 3.
Unique features of inorganic NMs can be leveraged to enhance anti-tumor immunity.
| Immune Setting | Inorganic NM | Effect | Ref. |
|---|---|---|---|
| Cancer | QDs | Promoted apoptosis in human pancreatic cancer cell line | 51 |
| AuNPs | Antigen-decoration delayed, reduced, or inhibited tumor growth in B16F10, B16-OVA and 4T1 cancer models. Efficacy in E.G7-OVA model was dependent on NP size. |
111 113 116 118 |
|
| Efficacy in B16-OVA cancer model was dependent on adjuvant choice for immune signal coating and injection route |
119 120 |
||
| poly(propylene sulfide) (PPS) NPs | Antigen and adjuvant delivery delayed EG.7-OVA tumor growth | 114 | |
| SWCNTs | Adjuvant attachment improved inhibition of cancer cell migration | 115 | |
| Antibody-coating targeted intratumor but not peripheral TREGs | 122 | ||
| Taken up by monocytes, entered tumor interstitium, and crossed blood vessel walls. | 125 | ||
| Ablation resulted in strong local and systemic anti-tumor response with memory | 131 | ||
| AuNRs | Combined irradiation and adjuvant delivery promoted protection from B16F10 tumors | 133 | |
| Silica NPs | Codelivery of OVA and CpG reduced B16-OVA tumor growth and suppressed tumor development following rechallenge. | 134 | |
| Cationic nature promotes tumor cell death and adjuvant delivery activates anti-tumor immune cell response | 135 | ||
| Iron oxide NPs | Magnetic targeting of IFN-γ coated NPs destroyed tumors | 136 | |
| DCs containing tumor lysates and heat shock protein-coated NPs increased survival in glioma model | 138 | ||
| Iron oxide-zinc oxide NPs | DCs containing antigen-coated NPs increased survival in CEA cancer model | 140 |