Department of Medicine, Baylor College of Medicine, Houston TX, United States.
Dan L Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX, United States.
Front Immunol. 2022 Jul 27;13:931612. doi: 10.3389/fimmu.2022.931612. eCollection 2022.
Peptide-based cancer vaccines have been shown to boost immune systems to kill tumor cells in cancer patients. However, designing an effective T cell epitope peptide-based cancer vaccine still remains a challenge and is a major hurdle for the application of cancer vaccines. In this study, we constructed for the first time a library of peptide-based cancer vaccines and their clinical attributes, named CancerVaccine (https://peptidecancervaccine.weebly.com/). To investigate the association factors that influence the effectiveness of cancer vaccines, these peptide-based cancer vaccines were classified into high (HCR) and low (LCR) clinical responses based on their clinical efficacy. Our study highlights that modified peptides derived from artificially modified proteins are suitable as cancer vaccines, especially for melanoma. It may be possible to advance cancer vaccines by screening for HLA class II affinity peptides may be an effective therapeutic strategy. In addition, the treatment regimen has the potential to influence the clinical response of a cancer vaccine, and Montanide ISA-51 might be an effective adjuvant. Finally, we constructed a high sensitivity and specificity machine learning model to assist in designing peptide-based cancer vaccines capable of providing high clinical responses. Together, our findings illustrate that a high clinical response following peptide-based cancer vaccination is correlated with the right type of peptide, the appropriate adjuvant, and a matched HLA allele, as well as an appropriate treatment regimen. This study would allow for enhanced development of cancer vaccines.
基于肽的癌症疫苗已被证明可以增强免疫系统,杀死癌症患者的肿瘤细胞。然而,设计一种有效的 T 细胞表位肽基癌症疫苗仍然是一个挑战,也是癌症疫苗应用的主要障碍。在这项研究中,我们首次构建了基于肽的癌症疫苗及其临床属性文库,命名为 CancerVaccine(https://peptidecancervaccine.weebly.com/)。为了研究影响癌症疫苗效果的关联因素,我们根据其临床疗效将这些基于肽的癌症疫苗分为高(HCR)和低(LCR)临床反应。我们的研究强调,源自人工修饰蛋白的修饰肽可用作癌症疫苗,特别是用于黑色素瘤。筛选与 HLA 类 II 亲和力肽匹配的疫苗可能是一种有效的治疗策略。此外,治疗方案有可能影响癌症疫苗的临床反应,Montanide ISA-51 可能是一种有效的佐剂。最后,我们构建了一个高灵敏度和特异性的机器学习模型,以协助设计能够提供高临床反应的基于肽的癌症疫苗。总之,我们的研究结果表明,基于肽的癌症疫苗接种后的高临床反应与正确的肽类型、适当的佐剂和匹配的 HLA 等位基因以及适当的治疗方案相关。这项研究将有助于增强癌症疫苗的开发。