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一种极简病原体样糖纳米疫苗,用于增强癌症免疫治疗。

A Minimalist Pathogen-Like Sugar Nanovaccine for Enhanced Cancer Immunotherapy.

机构信息

Institute of Functional Nano & Soft Materials (FUNSOM), Jiangsu Key Laboratory for Carbon-Based Functional Materials & Devices, Soochow University, Suzhou, 215123, China.

School of Materials Science and Engineering, Tongji University, Shanghai, 201804, China.

出版信息

Adv Mater. 2024 Nov;36(44):e2410715. doi: 10.1002/adma.202410715. Epub 2024 Aug 29.

Abstract

Pathogen-mimicking nanoparticles have emerged at the forefront of vaccine delivery technology, offering potent immune activation and excellent biocompatibility. Among these innovative carriers, mannan, a critical component of yeast cell walls, shows promise as an exemplary vaccine carrier. Nevertheless, it faces challenges like unpredictable immunogenicity, rapid elimination, and limited antigen loading due to high water solubility. Herein, mannan with varying carbon chain ratios is innovatively modified, yielding a series of dodecyl chains modified mannan (Mann-C). Through meticulous screening, a mannan variant with a 40% grafting ratio is pinpointed as the optimal vaccine carrier. Further RNA sequencing confirms that Mann-C exhibits desired immunostimulatory characteristics. Coupled with antigen peptides, Mann-C/OVA nanovaccine initiates the maturation of antigen-presenting cells by activating the TLR4 and Dectin-2 pathways, significantly boosting antigen utilization and sparking antigen-specific immune responses. In vivo, experiments utilizing the B16-OVA tumor model underscore the exceptional preventive capabilities of Mann-C/OVA. Notably, when combined with immune checkpoint blockade therapy, it displays a profound synergistic effect, leading to marked inhibition of tumor growth. Thus, the work has yielded a pathogen-like nanovaccine that is both simple to prepare and highly effective, underscoring the vast potential of mannan-modified nanovaccines in the realm of cancer immunotherapy.

摘要

病原体模拟纳米颗粒在疫苗递送技术领域崭露头角,具有强大的免疫激活作用和优异的生物相容性。在这些创新载体中,甘露聚糖作为酵母细胞壁的重要组成部分,有望成为一种理想的疫苗载体。然而,由于其高水溶性,甘露聚糖存在免疫原性不可预测、快速消除和抗原负载有限等挑战。在此,我们创新性地对具有不同碳链比例的甘露聚糖进行了修饰,得到了一系列十二烷基链修饰的甘露聚糖(Mann-C)。通过精心筛选,确定了一种接枝率为 40%的甘露聚糖变体作为最佳疫苗载体。进一步的 RNA 测序证实了 Mann-C 具有理想的免疫刺激特性。与抗原肽偶联后,Mann-C/OVA 纳米疫苗通过激活 TLR4 和 Dectin-2 途径诱导抗原呈递细胞的成熟,显著提高了抗原的利用率并引发了抗原特异性免疫反应。在体内,利用 B16-OVA 肿瘤模型进行的实验突出了 Mann-C/OVA 的优异预防能力。值得注意的是,当与免疫检查点阻断治疗联合使用时,它表现出显著的协同作用,导致肿瘤生长明显受到抑制。因此,这项工作得到了一种类似病原体的纳米疫苗,其制备简单且高效,突显了甘露聚糖修饰的纳米疫苗在癌症免疫治疗领域的巨大潜力。

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