Sun et al. report on a personized cancer vaccine generated by irradiating GM-CSF overexpressed tumor cells (providing antigens and stimulation signal for APCs), covalent conjugation with hyaluronic acid (improving the persistence of antigen stimulation). The engineered vaccine activated antitumor immunity responses and prevented tumor growth in mice with a single immunization.
Abstract:
Vaccine-based therapeutics for cancers face several challenges including lack of immunogenicity and tumor escape pathways for single antigen targets. It has been reported that radiotherapy has an in situ vaccine effect that provides tumor antigens following irradiation, helping to activate antigen-presenting cells (APCs). Herein, a new vaccine approach is developed by combining genetically engineered irradiated tumor cell debris (RTD) and hyaluronic acid (HA), termed HA@RTD. A cancer cell line is developed that overexpresses granulocyte-macrophage colony-stimulating factor (GM-CSF). A hydrogel was developed by covalent conjugation of HA with RTD proteins that acted as a potent vaccine system, the effects which were probed with T cell receptor sequencing. The engineered vaccine activated antitumor immunity responses and prevented tumor growth in mice even with a single immunization. HA@RTD vaccine efficacy was also assessed in therapeutic settings with established tumors and in combination with immune checkpoint blockade.
Author list:
Yajie Sun†, Yan Hu†, Yuanyuan Geng†, Chao Wan, Yang Liu, Yifei Liao, Xiujuan Shi, Jonathan F. Lovell, Kunyu Yang*, Honglin Jin*
How to cite:
Y. Sun, Y. Hu, Y. Geng, C. Wan, Y. Liu, Y. Liao, X. Shi, J. F. Lovell, K. Yang, H. Jin, Exploration 2024, 20220170.
https://doi.org/10.1002/EXP.20220170