Harnessing synthetic biology for advancing RNA therapeutics and vaccine design

被引:7
|
作者
Pfeifer, Blaine A. [1 ]
Beitelshees, Marie [2 ]
Hill, Andrew [2 ]
Bassett, Justin [1 ]
Jones, Charles H. [2 ]
机构
[1] Univ Buffalo State Univ New York, Dept Chem & Biol Engn, Buffalo, NY USA
[2] Pfizer, 66 Hudson Blvd, New York, NY 10001 USA
关键词
DELIVERY-SYSTEMS; LISTERIOLYSIN-O; GENE-EXPRESSION; MESSENGER-RNA; MURINE MODEL; GUIDE RNA; PROTEIN; APTAMERS; ANTIGEN; CONSTRUCTION;
D O I
10.1038/s41540-023-00323-3
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Recent global events have drawn into focus the diversity of options for combatting disease across a spectrum of prophylactic and therapeutic approaches. The recent success of the mRNA-based COVID-19 vaccines has paved the way for RNA-based treatments to revolutionize the pharmaceutical industry. However, historical treatment options are continuously updated and reimagined in the context of novel technical developments, such as those facilitated through the application of synthetic biology. When it comes to the development of genetic forms of therapies and vaccines, synthetic biology offers diverse tools and approaches to influence the content, dosage, and breadth of treatment with the prospect of economic advantage provided in time and cost benefits. This can be achieved by utilizing the broad tools within this discipline to enhance the functionality and efficacy of pharmaceutical agent sequences. This review will describe how synthetic biology principles can augment RNA-based treatments through optimizing not only the vaccine antigen, therapeutic construct, therapeutic activity, and delivery vector. The enhancement of RNA vaccine technology through implementing synthetic biology has the potential to shape the next generation of vaccines and therapeutics.
引用
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页数:10
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