ACS applied materials & interfaces · 2026
Personalized Biomineralized Tumor Whole-Component Vaccine for Synergistic cGAS-STING/aTIGIT Immunotherapy.
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Zhang Xuan, Shi Yuhao, Xie Songxiang, Yi Zineng, Jiang Zijun, Wang Yiduo, Zha Zhengbao
Аннотация
Conventional adjuvants such as aluminum salts rarely drive robust Th1 immunity, which limits cancer vaccine efficacy. A double-stranded DNA-loaded manganese phosphate nanoadjuvant was generated by dsDNA-templated biomimetic mineralization. The resulting DNA@MnP exhibited favorable physiological stability and pH-responsive release properties: at pH 5.5, the cumulative release rates of Mn2+ and DNA reached 72% and 78%, respectively, within 12 h. Following cytosolic delivery, released Mn2+ from DNA@MnP could augment the cGAS recognition of dsDNA. The cooperative action of Mn2+ and dsDNA produced cascade amplification that potently activated the cGAS-STING pathway in dendritic cells. In vitro experiments demonstrated that DNA@MnP significantly promoted the maturation of BMDCs (with a maturation rate 2.10-fold elevation compared with the control group) and induced RAW264.7 macrophages to polarize toward the M1 phenotype (with an M1/M2 ratio 8.31-fold elevation compared with the control group). Animal experiments demonstrated that DNA@MnP not only significantly enhanced antigen-specific humoral immunity, achieving a 16-fold increase in IgG titers, and elicited a balanced Th1/Th2 response but also effectively activated both innate and adaptive antitumor immunity. Furthermore, this platform was extended to develop a personalized tumor vaccine by encapsulating tumor lysates (TLs) into TLs-loaded manganese phosphate nanovaccines (TLs@MnP). When coadministered with an anti-TIGIT antibody, it potently suppressed tumor growth, recurrence, and metastasis: in the postoperative recurrence model, 42.9% of mice in the TLs@MnP multidose combined with aTIGIT group achieved long-term tumor-free survival. Therefore, this study presented a manganese phosphate-based biomineralization strategy for the concise preparation of autologous tumor vaccines, opening a promising avenue for personalized immunotherapy and clinical translation.
Предметные рубрики MeSH
AnimalsMiceCancer VaccinescGAS-STING Signaling PathwayImmunotherapyRAW 264.7 CellsNucleotidyltransferasesDNACyclic Guanosine Monophosphate-Adenosine Monophosphate SynthaseSTING ProteinFemaleHumansMembrane ProteinsNanovaccinesAdjuvants, ImmunologicDendritic CellsManganese CompoundsMice, Inbred C57BLNanoparticles