抗原
癌症研究
细胞毒性T细胞
免疫疗法
CD8型
肿瘤细胞
生物
免疫学
免疫系统
体外
生物化学
作者
Zeyu Yang,Liyan Li,Chengxiu Wei,Hong Liu,Dongdong Qiao,Zhenfu Wen,Haolin Chen,Shanghui Huang,Rui Guo,Zhinan Yin,Lixin Liu,Yongming Chen
标识
DOI:10.1002/adfm.202303537
摘要
Abstract Most vaccines are designed to attack tumor cells by activating CD4 + /CD8 + αβ T cells. Unfortunately, αβ T cells, which only recognize the peptide antigens in the complexes with polymorphic MHCI/II molecules, surrender to the tumor heterogenicity. As another subset of T cells, γδ T cells become salient in antitumor because of their unique immunotherapeutic roles. Herein, a tumor vaccine is developed with multivalent antigens by fusion of tumor cell membranes with lipids and successfully activated γδ T cells via microneedle inoculation. It is certified that the evoked γδ T cells synchronize with αβ T cells revitalizing tumor‐induced immunotolerance. In turn, the tumors of mice are significantly inhibited and their median survival time is prolonged considerably. Moreover, the nanovaccine inhibits tumor recurrence after resection. The therapeutic effects are corroborated with the results from TCR δ −/− mice as well as cytokine expression in tumor.
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