Tianjin Medical Journal ›› 2025, Vol. 53 ›› Issue (10): 1021-1026.doi: 10.11958/20251525

• Experimental Research • Previous Articles     Next Articles

Development and evaluation of the tumor vaccine TCL/CpG@GNP

CHEN Minchun(), XUE Runqing, ZHAO Xin, ZHANG Meng, YE Dan, ZHANG Jingyi, ZHENG Jie△()   

  1. Department of Pharmacy, Xi’an No.3 Hospital, the Affiliated Hospital of Northwest University, Xi’an 710018, China
  • Received:2025-05-10 Revised:2025-06-09 Published:2025-10-15 Online:2025-10-12
  • Contact: △E-mail:44682408@qq.com

Abstract:

Objective To develop a tumor vaccine containing broad-spectrum neoantigen tumor cell lysate (TCL) and CpG adjuvant, and to effectively deliver it to lymph node dendritic cells. Methods A novel polymer, 9-fluorenylmethoxycarbonyl-polyethylene glycol-glycocholic acid (Fmoc-PEG-GCA), was employed to encapsulate the TCL and CpG through π-π stacking, resulting in high-density polyethylene glycol-modified glycocholic acid-decorated micelles TCL/CpG@GNP. The vaccine's drug loading, encapsulation efficiency, particle size, polydispersity index (PDI), zeta potential, morphology, stability, cellular safety, uptake capability, immune stimulation effects on bone marrow-derived dendritic cells (BMDCs) and in vivo anti-tumor efficacy were evaluated. Results The vaccine TCL and CpG demonstrated a drug loading capacity of 6.26% and the encapsulation rate was 37.59%. The drug loading capacity of CpG was 7.05%, and the encapsulation efficiency was 56.86%. The particle size measured (139.26±27.23) nm, with a PDI of 0.249±0.015, indicating favorable dispersion properties. The zeta potential was recorded at (-21.23±0.36) mV. The TCL/CpG@GNP vaccine demonstrated good stability, cell safety and uptake ability, and can promote the activation and maturation of BMDCs. In tumor-bearing mouse models, TCL/CpG@GNP inhibited tumor growth, increased the proportion of T lymphocytes in peripheral blood, and elevated IFN-γ levels in spleen. Conclusion The TCL/CpG@GNP tumor vaccine can effectively activate BMDCs and induce strong anti-tumor immune memory in a mouse lung cancer model.

Key words: cancer vaccines, tumor cell lysates, CpG adjuvant, immunotherapy

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