The Role of Epidemic Tumor Vaccine in Cold Tumors to Hot Tumors
DOI:
https://doi.org/10.62051/abrm9r87Keywords:
Tumor vaccine; cold tumors; hot tumors.Abstract
Compared with hot tumors, cold tumors are a more difficult problem at present. Because cold tumors lack in congenital immunity, it is difficult for ordinary immune examination inhibitors to work. Therefore, how to "ignite" cold tumors as hot tumors is the focus of the current research. At present, scholars have proposed different and corresponding methods for various causes of T cell immunodeficiency. Among them, tumor vaccines stand out from the principle of activating the immune response of T cells and NK cells, and is currently generally recognized as a new therapy and research hotspot with strong anti-cancer activity. By classifying the target sites of tumor vaccines, they can be divided into tumor-related antigen (TAAs) vaccines and new antigen (TSAs) vaccines. Both vaccines have shown significant effects in activating T cells and NK cells. In terms of the current development status of the two vaccines, more and more research teams have invested in the research of TSAs vaccines, and many teams still insist on the research of TAAs vaccines. Although these two vaccines have their own difficulties to overcome, they still have made great contributions to the development of tumor treatment research, and both have advantages and broad prospects that cannot be reached by other methods. It is believed that no more effective tumor vaccines have been put into clinical trials.
Downloads
References
[1] Yuan-Tong Liu, et al. Turning cold tumors into hot tumors by improving T-cell infiltration. Theranostics, 2021, 11(11): 5365-5386.
[2] Bonaventura P, et al. Cold Tumors: A Therapeutic Challenge for Immunotherapy. Front Immunol, 2019, 10: 168.
[3] Ott P, Hu-Lieskovan S, Chmielowski B, et al. A Phase lb Trial of Personalized Neoantigen Therapy Plus Anti-PD-1 in Patients with Advanced Melanoma, Non-small Cell Lung Cancer, or Bladder Cancer. Cell, 2020, 183: 347-362.e24.
[4] Badrinath S, Dellacherie MO, Li A, et al. A vaccine targeting resistant tumours by dual T cell plus NK cell attack. Nature, 2022, 606: 992-998.
[5] Challenges in developing personalized neoantigen cancer vaccines. Nat Rev Immunol, 2023 Oct 2.
[6] Advances in the development of personalized neoantigen-based therapeutic cancer vaccines. Nat Rev Clin Oncol, 2021, 18(4): 215-229.
[7] Therapeutic cancer vaccines. Nat Rev Cancer, 2021 Apr 27.
[8] Tumeh PC, et al. PD-1 blockade induces responses by inhibiting adaptive immune resistance. Nature, 2014, 515(7528): 568-571.
[9] Mi Y, et al. The emerging role of myeloid-derived suppressor cells in the glioma immune suppressive microenvironment. Front Immunol, 2020, 11: 737.
[10] Srivastava P, et al. Immunomodulatory action of SGI-110, a hypomethylating agent, in acute myeloid leukemia cells. Leuk Res, 2014, 38: 1332.
[11] Zhang C, et al. Chimeric antigen receptor-engineered NK-92 cells: an off-the-shelf cellular therapeutic for targeted elimination of cancer cells and induction of protective antitumor immunity. Front Immunol, 2017, 8: 533.
[12] Ott PA, et al. An immunogenic personal neoantigen vaccine for patients with melanoma. Nature, 2017, 547: 217-221.
[13] Golden EB, et al. Radiotherapy and immunogenic cell death. Semin Radiat Oncol, 2015, 25(1): 11-17.
[14] Bevers RFM, et al. Role of urothelial cells in BCG immunotherapy for superficial bladder cancer. Br J Cancer, 2004, 91: 607-612.
[15] Khong A, et al. The use of agonistic anti-CD40 therapy in treatments for cancer. Int Rev Immunol, 2012, 31: 246-266.
[16] Ribas A, et al. Oncolytic Virotherapy Promotes Intratumoral T Cell Infiltration and Improves Anti-PD-1 Immunotherapy. Cell, 2017, 170(6): 1109-1119.e10.
[17] Shrimali RK, et al. Antiangiogenic agents can increase lymphocyte infiltration into tumor and enhance the effectiveness of adoptive immunotherapy of cancer. Cancer Res, 2010, 70(15): 6171-6180.
[18] Klein C, et al. Cergutuzumab amunaleukin (CEA-IL2v), a CEA-targeted IL-2 variant-based immunocytokine for combination cancer immunotherapy: overcoming limitations of aldesleukin and conventional IL-2-based immunocytokines.
[19] van der Burg SH, et al. Vaccines for established cancer: overcoming the challenges posed by immune evasion. Nat Rev Cancer, 2016, 16: 219-233.
[20] Liu J, Fu M, Wang M, Wan D, Wei Y, Wei X. Cancer vaccines as promising immuno-therapeutics: platforms and current progress. J Hematol Oncol, 2022, 15(1): 28.
[21] Robert E, Hollingsworth et al. Turning the corner on therapeutic cancer vaccines. npj Vaccines, 2020.
[22] Stine ZE, Schug ZT, Salvino JM, Dang CV. Targeting cancer metabolism in the era of precision oncology. Nat Rev Drug Discov, 2021.
[23] Rojas LA, Sethna Z, Soares KC, et al. Personalized RNA neoantigen vaccines stimulate T cells in pancreatic cancer. Nature, 2023, 618(7963): 144-150.
[24] Blass E, Ott PA. Advances in the development of personalized neoantigen-based therapeutic cancer vaccines. Nat Rev Clin Oncol, 2021, 18(4): 215-229.
Downloads
Published
Conference Proceedings Volume
Section
License

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.







