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Inhibition of tumor growth by cancer vaccine combined with metronomic chemotherapy and anti-PD-1 in a pre-clinical setting

机译:在临床前环境中通过癌症疫苗联合节律化疗和抗PD-1抑制肿瘤生长

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摘要

Tumor microenvironment (TME) is characterized by multiple immune suppressive mechanisms able to suppress anti-tumor effector cell immunity. Combinatorial strategies, including vaccine and immunomodulatory drugs, need to be developed for improved immunotherapy efficacy.A novel combinatorial approach was assessed in C57BL/6 mice injected with mouse melanoma B16F10 cells. A multi-peptide vaccine (PEPT) was combined with a low dose metronomic chemotherapy (MCT) and an anti-PD-1 checkpoint inhibitor (CI). Statistical analysis were performed with the unpaired two-sided Student’s t-test and ANOVA.Animals treated with the multi-peptide vaccine combined with MCT or CI showed remarkable delay in tumor growth and prolonged survival as compared to control groups. The multi-pronged combination including PEPT+MCT+CI was able to prolong survival in all mice and inhibit tumor growth in 66.6% of mice. All animals which did not show tumor growth were re-challenged with the same melanoma cells and one of them showed complete tumor growth inhibition. The anti-tumor effect was associated with strong T cell immune response to vaccine mutated peptides and significant reduction of regulatory T cells.The combination of a vaccine with MCT and CI was highly efficient in potentiating the vaccine’s anti-tumor effects. The approach is highly promising to be moved into clinical trial.
机译:肿瘤微环境(TME)的特征在于多种免疫抑制机制,能够抑制抗肿瘤效应细胞的免疫力。需要开发包括疫苗和免疫调节药物在内的组合策略以提高免疫疗法的效力。在注射了小鼠黑素瘤B16F10细胞的C57BL / 6小鼠中评估了一种新颖的组合方法。多肽疫苗(PEPT)与低剂量节律化疗(MCT)和抗PD-1检查点抑制剂(CI)结合使用。使用未配对的双面学生t检验和ANOVA进行统计分析。与对照组相比,多肽疫苗联合MCT或CI处理的动物显示出明显的肿瘤生长延迟和延长的生存期。包括PEPT + MCT + CI在内的多管齐下的组合能够延长所有小鼠的生存期,并抑制66.6%的小鼠的肿瘤生长。所有未表现出肿瘤生长的动物都被相同的黑色素瘤细胞再次攻击,其中一只表现出完全的肿瘤生长抑制。抗肿瘤作用与疫苗突变肽对T细胞的强烈免疫反应以及调节性T细胞的显着减少有关。疫苗与MCT和CI的组合可有效增强疫苗的抗肿瘤作用。该方法极有希望进入临床试验。

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