Photodynamic Therapy Derived Personalized Whole Cell Tumor Vaccine Prevents Postsurgery Tumor Recurrence and Metastasis

Author:

Yang Chunyu1,Jiang Yitong2,Zhang Kaixin1,Zhu Xianqi2,Li Jianlin2,Yu Haiwang2,Chen Jiawei2,Gu Xinggui13,Gan Zhihua2,Yu Qingsong2ORCID

Affiliation:

1. Beijing Advanced Innovation Center for Soft Matter Science and Engineering State Key Laboratory of Chemical Resource Engineering College of Materials Science and Engineering Beijing University of Chemical Technology Beijing 100029 China

2. The State Key Laboratory of Organic‐Inorganic Composites Beijing Laboratory of Biomedical Materials College of Life Science and Technology Beijing University of Chemical Technology Beijing 100029 China

3. Beijing National Laboratory for Molecular Sciences Beijing 100190 China

Abstract

AbstractIn order to avoid the time‐consuming and laborious identification of tumor‐specific antigens (TSAs) during the traditional vaccine fabrication process, a versatile photodynamic therapy (PDT)‐based method is developed to construct a whole‐tumor antigen tumor vaccine (TV) from surgically resected tumor tissues for personalized immunotherapy. Mucoadhesive nanoparticles containing small‐molecular photosensitizer are fabricated and directly co‐incubated with suspended tumor cells obtained after cytoreduction surgery. After irradiation with a 405 nm laser, potent immunogenic cell death of cancer cells could be induced. Along with the release of TSAs, the as‐prepared TV could activate safe and robust tumor‐specific immune responses, leading to efficient suppression of postsurgery tumor recurrence and metastasis. The as‐prepared TV cannot only be applied alone through various administration routes but also synergize with immunoadjuvant, chemotherapeutics, and immune checkpoint blockers to exert more potent immune responses. This work provides an alternative way to promote the clinical translation of PDT, which is generally restricted by the limited penetration of light. Moreover, the versatile strategy of vaccine fabrication also facilitates the clinical application of personalized whole‐cell tumor vaccines.

Funder

National Natural Science Foundation of China

Beijing National Laboratory for Molecular Sciences

Fundamental Research Funds for the Central Universities of Beijing University of Chemical Technology

Publisher

Wiley

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