Abstract
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.
| Original language | English |
|---|---|
| Article number | 103341 |
| Journal | Drug Discovery Today |
| Volume | 27 |
| Issue number | 11 |
| DOIs | |
| State | Published - Nov 2022 |
Bibliographical note
Publisher Copyright:© 2022 Elsevier Ltd
Funding
The authors would like to acknowledge the Research Center for Pharmaceutical Nanotechnology (RCPN) at Tabriz University of Medical Sciences for the support (#68182).
| Funders | Funder number |
|---|---|
| Tabriz University | 68182 |
ASJC Scopus Subject Areas
- Pharmacology
- Drug Discovery
Keywords
- Messenger RNA capping
- polymerase
- RNA-dependent RNA polymerase
- self-amplifying mRNA
- translation medicine
- vaccine
Disciplines
- Pharmacology
- Pharmaceutics and Drug Design
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