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免疫抑制逆转纳米疫苗用树突状细胞替代个性化癌症免疫疗法。

Immunosuppression Reversal Nanovaccines Substituting Dendritic Cells for Personalized Cancer Immunotherapy.

机构信息

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.

出版信息

Front Immunol. 2022 Jun 24;13:934259. doi: 10.3389/fimmu.2022.934259. eCollection 2022.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2545/9263089/ef781090a2cc/fimmu-13-934259-g001.jpg

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