Preston A. Wells Jr. Center for Brain Tumour Therapy, University of Florida, Gainesville, FL, USA.
Lillian S. Wells Department of Neurosurgery, University of Florida, Gainesville, FL, USA.
Nat Rev Clin Oncol. 2024 Jul;21(7):489-500. doi: 10.1038/s41571-024-00902-1. Epub 2024 May 17.
mRNA vaccines have been revolutionary in terms of their rapid development and prevention of SARS-CoV-2 infections during the COVID-19 pandemic, and this technology has considerable potential for application to the treatment of cancer. Compared with traditional cancer vaccines based on proteins or peptides, mRNA vaccines reconcile the needs for both personalization and commercialization in a manner that is unique to each patient but not beholden to their HLA haplotype. A further advantage of mRNA vaccines is the availability of engineering strategies to improve their stability while retaining immunogenicity, enabling the induction of complementary innate and adaptive immune responses. Thus far, no mRNA-based cancer vaccines have received regulatory approval, although several phase I-II trials have yielded promising results, including in historically poorly immunogenic tumours. Furthermore, many early phase trials testing a wide range of vaccine designs are currently ongoing. In this Review, we describe the advantages of cancer mRNA vaccines and advances in clinical trials using both cell-based and nanoparticle-based delivery methods, with discussions of future combinations and iterations that might optimize the activity of these agents.
mRNA 疫苗在 COVID-19 大流行期间在快速开发和预防 SARS-CoV-2 感染方面具有革命性意义,并且在癌症治疗方面具有相当大的应用潜力。与基于蛋白质或肽的传统癌症疫苗相比,mRNA 疫苗以独特的方式兼顾了个性化和商业化的需求,而不受其 HLA 单倍型的影响。mRNA 疫苗的另一个优势是能够利用工程策略来提高其稳定性,同时保持免疫原性,从而能够诱导互补的先天和适应性免疫反应。到目前为止,还没有基于 mRNA 的癌症疫苗获得监管部门的批准,尽管几项 I- II 期临床试验取得了可喜的结果,包括在历史上免疫原性较差的肿瘤中。此外,目前正在进行许多早期临床试验,测试广泛的疫苗设计。在这篇综述中,我们描述了癌症 mRNA 疫苗的优势以及使用基于细胞和基于纳米颗粒的递送方法的临床试验进展,并讨论了未来可能优化这些药物活性的组合和迭代。