Lee Karin L, Schlom Jeffrey, Hamilton Duane H
Laboratory of Tumor Immunology and Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Cancer Immunol Immunother. 2021 Apr;70(4):875-885. doi: 10.1007/s00262-020-02729-y. Epub 2020 Oct 8.
Clinical successes have been achieved with checkpoint blockade therapy, which facilitates the function of T cells recognizing tumor-specific mutations known as neoepitopes. It is a reasonable hypothesis that therapeutic cancer vaccines targeting neoepitopes uniquely expressed by a patient's tumor would prove to be an effective therapeutic strategy. With the advent of high-throughput next generation sequencing, it is now possible to rapidly identify these tumor-specific mutations and produce therapeutic vaccines targeting these patient-specific neoepitopes. However, initial reports suggest that when used as a monotherapy, neoepitope-targeted vaccines are not always sufficient to induce clinical responses in some patients. Therefore, research has now turned to investigating neoepitope vaccines in combination with other cancer therapies, both immune and non-immune, to improve their clinical efficacies.
检查点阻断疗法已取得临床成功,该疗法可促进识别被称为新抗原的肿瘤特异性突变的T细胞的功能。一个合理的假设是,针对患者肿瘤独特表达的新抗原的治疗性癌症疫苗将被证明是一种有效的治疗策略。随着高通量下一代测序技术的出现,现在有可能快速识别这些肿瘤特异性突变,并生产针对这些患者特异性新抗原的治疗性疫苗。然而,初步报告表明,当作为单一疗法使用时,新抗原靶向疫苗在某些患者中并不总是足以诱导临床反应。因此,现在的研究转向研究新抗原疫苗与其他癌症疗法(包括免疫疗法和非免疫疗法)联合使用,以提高其临床疗效。