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. Author manuscript; available in PMC: 2020 Aug 1.
Published in final edited form as: Nano Today. 2019 May 29;27:73–98. doi: 10.1016/j.nantod.2019.04.005

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