Cancer-Targetable pH-Sensitive Zinc-Based Immunomodulators Combined with Photodynamic Therapy for in Situ Vaccination
Source abstract
Abstract
A cancer vaccine is a promising immunotherapy modality, but the heterogenicity of tumors and substantial time and costs required in tumor-associated antigen (TAA) screening have hindered the development of an individualized vaccine. Herein, we propose in situ vaccination using cancer-targetable pH-sensitive zinc-based immunomodulators (CZIs) to elicit antitumor immune response against TAAs of patients’ tumors without the ex vivo identification processes. In the tumor microenvironment, CZIs promote the release of large amounts of TAAs and exposure of calreticulin on the cell surface via immunogenic cell death through the combined effect of excess zinc ions and photodynamic therapy (PDT). With these properties, CZIs potentiate antitumor immunity and inhibit tumor growth as well as lung metastasis in CT26 tumor-bearing mice. This nanoplatform may suggest an alternative therapeutic strategy to overcoming the limitations of existing cancer vaccines and may broaden the application of nanoparticles for cancer immunotherapy.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Nanoplatforms for cancer theranostics · Immunotherapy and Immune Responses · Photodynamic Therapy Research Studies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Center for Photomedicine, Department of Biotechnology, The Catholic University of Korea, Bucheon-si, Gyeonggi do 14662, Republic of Korea
Department of Biomedical-Chemical Engineering, The Catholic University of Korea, Bucheon-si, Gyeonggi do 14662, Republic of Korea
Funding
National Research Foundation of Korea
References (29)
Show source-provided references
1. 10.1002/anie.20180488210.1002/anie.201804882 ↗
2. 10.1155/2014/73451510.1155/2014/734515 ↗
3. 10.1038/s41541-019-0103-y10.1038/s41541-019-0103-y ↗
4. 10.1128/cvi.00286-1010.1128/cvi.00286-10 ↗
5. 10.1136/bmj.h98810.1136/bmj.h988 ↗
6. 10.2217/imt.15.12010.2217/imt.15.120 ↗
7. 10.1080/21645515.2015.104977910.1080/21645515.2015.1049779 ↗
8. 10.1039/c8nr01376d10.1039/c8nr01376d ↗
9. 10.1016/j.molonc.2015.10.01610.1016/j.molonc.2015.10.016 ↗
10. 10.1038/nnano.2015.29210.1038/nnano.2015.292 ↗
11. 10.1016/j.vaccine.2015.05.10510.1016/j.vaccine.2015.05.105 ↗
12. 10.1021/acsomega.8b0022710.1021/acsomega.8b00227 ↗
13. 10.1007/s12274-018-2124-710.1007/s12274-018-2124-7 ↗
14. 10.1016/j.clim.2014.05.00210.1016/j.clim.2014.05.002 ↗
15. 10.1007/s10495-017-1413-z10.1007/s10495-017-1413-z ↗
16. 10.1016/j.biomaterials.2019.01.01510.1016/j.biomaterials.2019.01.015 ↗
17. 10.2147/ijn.s1658110.2147/ijn.s16581 ↗
18. 10.1016/j.nano.2010.10.00110.1016/j.nano.2010.10.001 ↗
19. 10.1016/j.biomaterials.2014.08.02910.1016/j.biomaterials.2014.08.029 ↗
20. 10.1039/c7ra12969f10.1039/c7ra12969f ↗
21. 10.1016/j.polymer.2017.04.06310.1016/j.polymer.2017.04.063 ↗
22. 10.1021/acs.biomac.9b0032110.1021/acs.biomac.9b00321 ↗
23. 10.1016/j.progpolymsci.2019.05.00210.1016/j.progpolymsci.2019.05.002 ↗
24. 10.1038/nrc107110.1038/nrc1071 ↗
25. 10.1007/s40005-017-0377-x10.1007/s40005-017-0377-x ↗
26. 10.1586/eci.10.8110.1586/eci.10.81 ↗
27. 10.1002/ange.20191142910.1002/ange.201911429 ↗
28. 10.1021/acsami.6b0166410.1021/acsami.6b01664 ↗
29. 10.1038/s41577-019-0210-z10.1038/s41577-019-0210-z ↗