作者
Andrew J Geall, Ayush Verma, Gillis R Otten, Christine A Shaw, Armin Hekele, Kaustuv Banerjee, Yen Cu, Clayton W Beard, Luis A Brito, Thomas Krucker, Derek T O’Hagan, Manmohan Singh, Peter W Mason, Nicholas M Valiante, Philip R Dormitzer, Susan W Barnett, Rino Rappuoli, Jeffrey B Ulmer, Christian W Mandl
发表日期
2012/9/4
期刊
Proceedings of the National Academy of Sciences
卷号
109
期号
36
页码范围
14604-14609
出版商
National Academy of Sciences
简介
Despite more than two decades of research and development on nucleic acid vaccines, there is still no commercial product for human use. Taking advantage of the recent innovations in systemic delivery of short interfering RNA (siRNA) using lipid nanoparticles (LNPs), we developed a self-amplifying RNA vaccine. Here we show that nonviral delivery of a 9-kb self-amplifying RNA encapsulated within an LNP substantially increased immunogenicity compared with delivery of unformulated RNA. This unique vaccine technology was found to elicit broad, potent, and protective immune responses, that were comparable to a viral delivery technology, but without the inherent limitations of viral vectors. Given the many positive attributes of nucleic acid vaccines, our results suggest that a comprehensive evaluation of nonviral technologies to deliver self-amplifying RNA vaccines is warranted.
引用总数
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学术搜索中的文章
AJ Geall, A Verma, GR Otten, CA Shaw, A Hekele… - Proceedings of the National Academy of Sciences, 2012