CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Biodegradable MnO(2)-based gene-engineered nanocomposites for chemodynamic therapy and enhanced antitumor immunity.
Biodegradable MnO(2)-based gene-engineered nanocomposites for chemodynamic therapy and enhanced antitumor immunity.
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免疫检查点阻断(ICB)正逐渐成为一种有前景的临床治疗多种癌症的方法。然而,基于ICB的单一疗法仍因TIL(肿瘤浸润淋巴细胞)数量有限且耗竭以及肿瘤免疫抑制微环境而导致免疫缓解率较低。在本研究中,制备了表面展示PD-1蛋白的细胞膜(PD1-CM)用于免疫检查点阻断,并将其进一步与多功能且可生物降解的MnO₂结合,以实现系统且强效的抗肿瘤治疗。基于MnO₂的基因工程纳米复合材料可催化TME中丰富的H₂O₂分解生成O₂,从而促进T细胞向肿瘤内浸润,进而通过PD1-CM上的PD-1蛋白提高免疫检查点阻断的效果。此外,纳米复合材料中的MnO₂可完全降解为Mn²⁺,其可催化生成高毒性的羟基自由基用于化学动力学治疗,从而进一步增强治疗效果。此外,所制备的纳米复合材料具有成本低、制备简便和良好生物相容性的优势,有望成为联合免疫治疗的有前景的制剂。
Immune checkpoint blockade (ICB) is emerging as a promising therapeutic approach for clinical treatment against various cancers.
However, ICB based monotherapies still suffer from low immune response rate due to the limited and exhausted tumor-infiltrating lymphocytes as well as tumor immunosuppressive microenvironment. In this work, the cell membrane with surface displaying PD-1 proteins (PD1-CM) was prepared for immune checkpoint blockade, which was further combined with multifunctional and biodegradable MnO 2 for systematic and robust antitumor therapy.
The MnO 2 -based gene-engineered nanocomposites can catalyze the decomposition of abundant H 2 O 2 in TME to generate O 2 , which can promote the intratumoral infiltration of T cells, and thus improve the effect of immune checkpoint blockade by PD-1 proteins on PD1-CM.
Furthermore, MnO 2 in the nanocomposites can be completely degraded into Mn 2+ , which can catalyze the generation of highly toxic hydroxyl radicals for chemodynamic therapy, thereby further enhancing the therapeutic effect.
In addition, the prepared nanocomposites possess the advantages of low cost, easy preparation and good biocompatibility, which are expected to become promising agents for combination immunotherapy.
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