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用于针对神经胶质瘤的个体化免疫治疗的合成高密度脂蛋白纳米盘。

Synthetic High-density Lipoprotein Nanodiscs for Personalized Immunotherapy Against Gliomas.

机构信息

Department of Pharmaceutical Sciences, University of Michigan, Ann Arbor, Michigan.

Biointerfaces Institute, University of Michigan, Ann Arbor, Michigan.

出版信息

Clin Cancer Res. 2020 Aug 15;26(16):4369-4380. doi: 10.1158/1078-0432.CCR-20-0341. Epub 2020 May 21.

Abstract

PURPOSE

Gliomas are brain tumors with dismal prognoses. The standard-of-care treatments for gliomas include surgical resection, radiation, and temozolomide administration; however, they have been ineffective in providing significant increases in median survival. Antigen-specific cancer vaccines and immune checkpoint blockade may provide promising immunotherapeutic approaches for gliomas.

EXPERIMENTAL DESIGN

We have developed immunotherapy delivery vehicles based on synthetic high-density lipoprotein (sHDL) loaded with CpG, a Toll-like receptor-9 agonist, and tumor-specific neoantigens to target gliomas and elicit immune-mediated tumor regression.

RESULTS

We demonstrate that vaccination with neoantigen peptide-sHDL/CpG cocktail in combination with anti-PD-L1 immune checkpoint blocker elicits robust neoantigen-specific T-cell responses against GL261 cells and eliminated established orthotopic GL261 glioma in 33% of mice. Mice remained tumor free upon tumor cell rechallenge in the contralateral hemisphere, indicating the development of immunologic memory. Moreover, in a genetically engineered murine model of orthotopic mutant IDH1 (mIDH1) glioma, sHDL vaccination with mIDH1 neoantigen eliminated glioma in 30% of animals and significantly extended the animal survival, demonstrating the versatility of our approach in multiple glioma models.

CONCLUSIONS

Overall, our strategy provides a general roadmap for combination immunotherapy against gliomas and other cancer types.

摘要

目的

神经胶质瘤是预后不良的脑肿瘤。神经胶质瘤的标准治疗方法包括手术切除、放疗和替莫唑胺给药;然而,它们在提高中位生存期方面并没有显著效果。抗原特异性癌症疫苗和免疫检查点阻断可能为神经胶质瘤提供有前途的免疫治疗方法。

实验设计

我们已经开发了基于载有 CpG(一种 Toll 样受体 9 激动剂)和肿瘤特异性新抗原的合成高密度脂蛋白(sHDL)的免疫治疗载体,以靶向神经胶质瘤并引发免疫介导的肿瘤消退。

结果

我们证明,用新抗原肽-sHDL/CpG 鸡尾酒进行疫苗接种,联合抗 PD-L1 免疫检查点阻断剂,可引发针对 GL261 细胞的强烈新抗原特异性 T 细胞反应,并消除 33%的小鼠中已建立的原位 GL261 神经胶质瘤。在对侧半球重新挑战肿瘤细胞时,小鼠仍然没有肿瘤,表明免疫记忆的发展。此外,在原位突变 IDH1(mIDH1)神经胶质瘤的基因工程小鼠模型中,mIDH1 新抗原的 sHDL 疫苗接种可消除 30%的动物中的神经胶质瘤,并显著延长动物的存活期,证明了我们的方法在多种神经胶质瘤模型中的多功能性。

结论

总体而言,我们的策略为针对神经胶质瘤和其他癌症类型的联合免疫治疗提供了一个通用路线图。

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