免疫原性
行动方式
生物
信使核糖核酸
免疫系统
免疫学
计算机科学
计算生物学
遗传学
基因
生物化学
作者
Mohammad M. Pourseif,Yosef Masoudi-Sobhanzadeh,Erfan Azari,Sepideh Parvizpour,Jaleh Barar,Rais A. Ansari,Yadollah Omidi
标识
DOI:10.1016/j.drudis.2022.103341
摘要
The mRNA-based vaccines are quality-by-design (QbD) immunotherapies that provide safe, tunable, scalable, streamlined and potent treatment possibilities against different types of diseases. The self-amplifying mRNA (saRNA) vaccines, as a highly advantageous class of mRNA vaccines, are inspired by the intracellular self-multiplication nature of some positive-sense RNA viruses. Such vaccine platforms provide a relatively increased expression level of vaccine antigen(s) together with self-adjuvanticity properties. Lined with the QbD saRNA vaccines, essential optimizations improve the stability, safety, and immunogenicity of the vaccine constructs. Here, we elaborate on the concepts and mode-of-action of mRNA and saRNA vaccines, articulate the potential limitations or technical bottlenecks, and explain possible solutions or optimization methods in the process of their design and development.
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