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  2. NIR-II Multimodal Phototheranostics Synergized with Antigen-Specific Vaccines for Boosted Cancer Photoimmunotherapy

NIR-II Multimodal Phototheranostics Synergized with Antigen-Specific Vaccines for Boosted Cancer Photoimmunotherapy

  • ACS Nano. 2026 Jan 20;20(2):1928-1944. doi: 10.1021/acsnano.5c12430.
Hao Yang 1 2 Zhe Sun 3 4 Zhijun Zhang 1 Shanliang Song 1 Haifei Wen 1 Zengming Yang 1 2 Xue Li 1 Shuo Xiang 1 2 Lei Wang 1 Miaomiao Kang 1 Dong Wang 1 Ben Zhong Tang 5
Affiliations

Affiliations

  • 1 Center for AIE Research, Shenzhen Key Laboratory of Polymer Science and Technology, College of Materials Science and Engineering, Shenzhen University, Shenzhen 518060, China.
  • 2 College of Physics and Optoelectronic Engineering, Shenzhen University, Shenzhen 518060, China.
  • 3 Shenzhen Key Laboratory of Cardiovascular Disease, Fuwai Hospital Chinese Academy of Medical Sciences, Shenzhen 518038, China.
  • 4 Pingyang Affiliated Hospital of Wenzhou Medical University, Wenzhou 325400, China.
  • 5 Guangdong Basic Research Center of Excellence for Aggregate Science, School of Science and Engineering, The Chinese University of Hong Kong, Shenzhen, Guangdong 518172, China.
Abstract

Photoimmunotherapy offers precise tumor ablation and systemic immunity through immunogenic cell death and cytotoxic T-cell activation. Among immunotherapies, antigen-specific vaccines targeting well-defined tumor antigens are particularly promising for personalized Cancer treatment due to their durable immune surveillance and precise activation with minimal off-target effects. However, their integration with phototherapy remains almost unexplored. Herein, we report a synergistic strategy combining an antigen-specific vaccine with phototherapy. Specifically, motivated by the advantageous merits of multimodal phototheranostics, a multimodal phototheranostic agent (TBBSD) was rationally designed as the phototherapy module, while the hepatocellular carcinoma (HCC)-specific antigen glypican-3 (GPC3) protein and Adjuvant cyclic diadenylate (c-di-AMP) were employed as the antigen-specific vaccine. By means of the complementary advantages, this photoimmunotherapeutic strategy achieves efficient ablation of primary tumors, simultaneously induces a robust systemic immune response, and fosters long-term immunological memory, which synergistically prevents tumor recurrence and suppresses the growth of both distant and pulmonary metastatic lesions. Collectively, these results underscore the therapeutic reliability and translational potential of this efficacious photoimmunotherapy strategy for precision Cancer treatment.

Keywords

aggregation-induced NIR-II emission; antigen-specific vaccines; multimodal phototheranostics; photoimmunotherapy; synergistic treatment.

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