Kakwere Hamilton, Ingham Elizabeth S, Allen Riley, Mahakian Lisa M, Tam Sarah M, Zhang Hua, Silvestrini Matthew T, Lewis Jamal S, Ferrara Katherine W
Department of Biomedical Engineering, University of California , Davis, California 95616, United States.
Bioconjug Chem. 2017 Nov 15;28(11):2756-2771. doi: 10.1021/acs.bioconjchem.7b00502. Epub 2017 Oct 13.
Personalized cancer vaccines (PCVs) are receiving attention as an avenue for cancer immunotherapy. PCVs employ immunogenic peptide epitopes capable of stimulating the immune system to destroy cancer cells with great specificity. Challenges associated with effective delivery of these peptides include poor solubility of hydrophobic sequences, rapid clearance, and poor immunogenicity, among others. The incorporation of peptides into nanoparticles has the potential to overcome these challenges, but the broad range of functionalities found in amino acids presents a challenge to conjugation due to possible interferences and lack of reaction specificity. Herein, a facile and versatile approach to generating nanosized PCVs under mild nonstringent conditions is reported. Following a simple two-step semibatch synthetic approach, amphiphilic hyperbranched polymer-peptide conjugates were prepared by the conjugation of melanoma antigen peptides, either TRP2 (hydrophobic) or MUT30 (hydrophilic), to an alkyne functionalized core via strain-promoted azide-alkyne click chemistry. Self-assembly of the amphiphiles gave spherical nanovaccines (by transmission electron microscopy) with sizes in the range of 10-30 nm (by dynamic light scattering). Fluorescently labeled nanovaccines were prepared to investigate the cellular uptake by antigen presenting cells (dendritic cells), and uptake was confirmed by flow cytometry and microscopy. The TRP2 nanovaccine was taken up the most followed by MUT30 nanoparticles and, finally, nanoparticles without peptide. The nanovaccines showed good biocompatibility against B16-F10 cells, yet the TRP2 peptide showed signs of toxicity, possibly due to its hydrophobicity. A test for immunogenicity revealed that the nanovaccines were poorly immunogenic, implying the need for an adjuvant when administered in vivo. Treatment of mice with melanoma tumors showed that in combination with adjuvant, CpG, groups with the peptide nanovaccines slowed tumor growth and improved survival (up to 24 days, TRP2) compared to the untreated group (14 days).
个性化癌症疫苗(PCV)作为癌症免疫治疗的一种途径正受到关注。PCV采用能够刺激免疫系统以高度特异性破坏癌细胞的免疫原性肽表位。与这些肽的有效递送相关的挑战包括疏水序列的溶解性差、快速清除以及免疫原性差等。将肽掺入纳米颗粒有可能克服这些挑战,但由于可能的干扰和缺乏反应特异性,氨基酸中发现的广泛功能对缀合提出了挑战。在此,报道了一种在温和非严格条件下生成纳米级PCV的简便通用方法。采用简单的两步半间歇合成方法,通过应变促进的叠氮化物-炔烃点击化学将黑色素瘤抗原肽(TRP2(疏水)或MUT30(亲水))与炔烃功能化核心缀合,制备了两亲性超支化聚合物-肽缀合物。两亲物的自组装产生了球形纳米疫苗(通过透射电子显微镜观察),其尺寸范围为10-30nm(通过动态光散射)。制备了荧光标记的纳米疫苗以研究抗原呈递细胞(树突状细胞)的细胞摄取,并通过流式细胞术和显微镜确认摄取。TRP2纳米疫苗的摄取量最高,其次是MUT30纳米颗粒,最后是不含肽的纳米颗粒。纳米疫苗对B16-F10细胞显示出良好的生物相容性,但TRP2肽显示出毒性迹象,可能是由于其疏水性。免疫原性测试表明纳米疫苗的免疫原性较差,这意味着在体内给药时需要佐剂。对患有黑色素瘤肿瘤的小鼠进行治疗表明,与佐剂CpG联合使用时,肽纳米疫苗组与未治疗组(14天)相比,减缓了肿瘤生长并提高了生存率(TRP2组高达24天)。