Bioconjug Chem. 2018 Mar 21;29(3):771-775. doi: 10.1021/acs.bioconjchem.7b00761. Epub 2018 Feb 27.
While cancer immunotherapy provides new exciting treatment options for patients, there is an urgent need for new strategies that can synergize with immune checkpoint blockers and boost the patient response rates. We have developed a personalized vaccine nanodisc platform based on synthetic high-density lipoproteins for co-delivery of immunostimulatory agents and tumor antigens, including tumor-specific neoantigens. Here we examined the route of delivery, safety profiles, and therapeutic efficacy of nanodisc vaccination against established tumors. We report that nanodiscs administered via the subcutaneous (SC) or intramuscular (IM) routes were well tolerated in mice without any signs of toxicity. The SC route significantly enhanced nanoparticle delivery to draining lymph nodes, improved nanodisc uptake by antigen-presenting cells, and generated 7-fold higher frequency of neoantigen-specific T cells, compared with the IM route. Importantly, when mice bearing advanced B16F10 melanoma tumors were treated with nanodiscs plus anti-PD-1 and anti-CTLA-4 IgG therapy, the combination immunotherapy exerted potent antitumor efficacy, leading to eradication of established tumors in ∼60% of animals. These results demonstrate nanodiscs customized with patient-specific tumor neoepitopes as a safe and powerful vaccine platform for immunotherapy against advanced cancer.
虽然癌症免疫疗法为患者提供了新的令人兴奋的治疗选择,但仍迫切需要新的策略,以与免疫检查点抑制剂协同作用,提高患者的反应率。我们已经开发了一种基于合成高密度脂蛋白的个性化疫苗纳米盘平台,用于共递送免疫刺激剂和肿瘤抗原,包括肿瘤特异性新抗原。在这里,我们研究了纳米盘疫苗接种对已建立肿瘤的递送途径、安全性和治疗效果。我们报告说,皮下(SC)或肌肉内(IM)途径给药的纳米盘在小鼠中耐受性良好,没有任何毒性迹象。与 IM 途径相比,SC 途径显著增强了纳米颗粒向引流淋巴结的递送,提高了抗原呈递细胞对纳米盘的摄取,并产生了 7 倍以上的新抗原特异性 T 细胞频率。重要的是,当用纳米盘加抗 PD-1 和抗 CTLA-4 IgG 治疗法治疗携带晚期 B16F10 黑色素瘤肿瘤的小鼠时,联合免疫疗法发挥了强大的抗肿瘤疗效,导致约 60%的动物体内已建立的肿瘤被消除。这些结果表明,用患者特异性肿瘤新表位定制的纳米盘作为一种安全有效的免疫治疗先进癌症的疫苗平台。