State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics and Center for Molecular Imaging and Translational Medicine, School of Public Health, Xiamen University, Xiamen, China.
Front Immunol. 2022 Jun 24;13:934259. doi: 10.3389/fimmu.2022.934259. eCollection 2022.
Although immunotherapy has paved a new avenue for cancer treatment, inadequate immune response often executes suboptimal therapeutic effects. In general, an effective immune response undergoes presentation of antigen by antigen-presenting cells, proliferation and differentiation of lymphocytes, and attack of cancer cells by cytotoxic T lymphocytes (CTLs). The antigen self-presentation and immunosuppression reversal (ASPIRE) nanovaccine derived from dendritic cells provides a simplified and immune deregulated procedure for immunotherapy profiting from its orientable peculiarity. By integrating major histocompatibility complex class I (MHC-I) molecules into present specific epitopes and co-delivering anti-PD-1 antibody and B7 costimulatory molecules through the programmed biomimetic synthesis, the ASPIRE nanovaccine demonstrates a milestone in personalized cancer immunotherapy.
虽然免疫疗法为癌症治疗开辟了新途径,但免疫反应不足常常导致治疗效果不佳。一般来说,有效的免疫反应经历抗原呈递细胞对抗原的呈递、淋巴细胞的增殖和分化,以及细胞毒性 T 淋巴细胞(CTL)对癌细胞的攻击。树突状细胞衍生的抗原自身呈递和免疫抑制逆转(ASPIRE)纳米疫苗通过其定向特性为免疫疗法提供了简化和免疫调节程序,从而从中受益。通过将主要组织相容性复合体 I 类(MHC-I)分子整合到现有特异性表位中,并通过程序化仿生合成共同递呈抗 PD-1 抗体和 B7 共刺激分子,ASPIRE 纳米疫苗在个性化癌症免疫治疗方面取得了里程碑式的进展。