He Qing, Gao Hua, Tan Dejiang, Zhang Heng, Wang Jun-Zhi
National Institutes for Food and Drug Control, State Key Laboratory for Evaluation and Standardization of Innovative Vaccines and Biotechnology Products, Beijing 102629, China.
Acta Pharm Sin B. 2022 Jul;12(7):2969-2989. doi: 10.1016/j.apsb.2022.03.011. Epub 2022 Mar 23.
Patients exhibit good tolerance to messenger ribonucleic acid (mRNA) vaccines, and the choice of encoded molecules is flexible and diverse. These vaccines can be engineered to express full-length antigens containing multiple epitopes without major histocompatibility complex (MHC) restriction, are relatively easy to control and can be rapidly mass produced. In 2021, the U.S. Food and Drug Administration (FDA) approved the first mRNA-based coronavirus disease 2019 (COVID-19) vaccine produced by Pfizer and BioNTech, which has generated enthusiasm for mRNA vaccine research and development. Based on the above characteristics and the development of mRNA vaccines, mRNA cancer vaccines have become a research hotspot and have undergone rapid development, especially in the last five years. This review analyzes the advances in mRNA cancer vaccines from various perspectives, including the selection and expression of antigens/targets, the application of vectors and adjuvants, different administration routes, and preclinical evaluation, to reflect the trends and challenges associated with these vaccines.
患者对信使核糖核酸(mRNA)疫苗表现出良好的耐受性,并且编码分子的选择灵活多样。这些疫苗可以被设计成表达含有多个表位的全长抗原,而无需主要组织相容性复合体(MHC)限制,相对易于控制且能够快速大规模生产。2021年,美国食品药品监督管理局(FDA)批准了辉瑞公司和BioNTech公司生产的首款基于mRNA的2019冠状病毒病(COVID-19)疫苗,这激发了人们对mRNA疫苗研发的热情。基于上述特性以及mRNA疫苗的发展,mRNA癌症疫苗已成为一个研究热点并经历了快速发展,尤其是在过去五年中。本综述从多个角度分析了mRNA癌症疫苗的进展,包括抗原/靶点的选择与表达、载体和佐剂的应用、不同给药途径以及临床前评估,以反映这些疫苗相关的趋势和挑战。