Key Laboratory of Organic Optoelectronics and Molecular Engineering, Department of Chemistry, Tsinghua University, Beijing, 100084, China.
Department of Biomedical Engineering, Columbia University, New York, NY, 10032, USA.
Biomaterials. 2022 Jan;280:121321. doi: 10.1016/j.biomaterials.2021.121321. Epub 2021 Dec 14.
NK cell-based immunotherapy and pemetrexed (Pem)-based chemotherapy have broad application prospects in cancer treatment. However, the over-expressed NK cell inhibitory receptor on the surface of cancer cells and the low cell internalization efficiency of Pem greatly limit their clinical application. Herein, we construct a series of selenium-containing nanoparticles to synergistically enhance Pem-based chemotherapy and NK cell-based immunotherapy. The nanoparticles could deliver Pem to tumor sites and strengthen the chemotherapy efficiency of Pem by seleninic acid, which is produced by the oxidation of β-seleno ester. Moreover, seleninic acid can block the expression of inhibitory receptors against NK cells, thereby activating the immunocompetence of NK cells. The in vitro and in vivo experiments reveal the potential chemo-enhancing and immune-activating mechanism of seleninic acid, emphasizing the promising prospects of this strategy in effective chemoimmunotherapy.
基于自然杀伤(NK)细胞的免疫疗法和培美曲塞(Pem)为基础的化疗在癌症治疗中有广泛的应用前景。然而,癌细胞表面过度表达的 NK 细胞抑制受体和 Pem 的低细胞内化效率极大地限制了它们的临床应用。在这里,我们构建了一系列含硒纳米粒子,以协同增强基于 Pem 的化疗和基于 NK 细胞的免疫疗法。这些纳米粒子可以将 Pem 递送到肿瘤部位,并通过硒酸增强 Pem 的化疗效率,硒酸是由β-硒酯氧化产生的。此外,硒酸可以阻断抑制 NK 细胞的受体的表达,从而激活 NK 细胞的免疫能力。体外和体内实验揭示了硒酸的潜在化疗增强和免疫激活机制,强调了这一策略在有效化疗免疫治疗中的广阔前景。