Cited by 57RNA Interference and Gene DeliveryImmunotherapy and Immune ResponsesRNA and protein synthesis mechanisms

RNActive® Technology: Generation and Testing of Stable and Immunogenic mRNA Vaccines

Rauch, Susanne, Lutz, Johannes, Kowalczyk, Aleksandra, Schlake, Thomas, Heidenreich, Regina·2017·Methods in Molecular Biology

Abstract

Developing effective mRNA vaccines poses certain challenges concerning mRNA stability and ability to induce sufficient immune stimulation and requires a specific panel of techniques for production and testing. Here, we describe the production of stabilized mRNA with enhanced immunogenicity, generated using conventional nucleotides only, by introducing changes to the mRNA sequence and by complexation with the nucleotide-binding peptide protamine (RNActive® technology). Methods described here include the synthesis, purification, and protamine complexation of mRNA vaccines as well as a comprehensive panel of in vitro and in vivo methods for evaluation of vaccine quality and immunogenicity.

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Crossref · 10.1007/978-1-4939-6481-9_5

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  • The RNActive® platform designed by CureVac combines the use of co-delivered RNA and protamine (a polycationic peptide) complex as adjuvant, which has been shown to effectively trigger innate immune responses and enhance vaccine immunogenicity.

    “A vaccine platform (RNActive®) was designed by CureVac186 combining the use of co-delivered RNA and protamine (a polycationic peptide) complex as adjuvant, which has been shown to effectively trigger innate immune responses and enhance vaccine immunogenicity.186–189”

    From Advances in COVID-19 mRNA vaccine development (2022) · cites this paper as [186]

  • The favorable safety profile of the CVnCoV vaccine candidate was confirmed at up to a 12 μg dose.

    “The favorable safety profile of the CVnCoV vaccine candidate126,127 using the RNActive mRNA vaccine platform developed by CureVac128 was confirmed at up to a 12 μg dose,129”

    From COVID-19 mRNA vaccines: Platforms and current developments (2022) · cites this paper as [128]

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References 15 · Cited by 57

Authors
Rauch, S., Lutz, J., Kowalczyk, A., Schlake, T., & Heidenreich, R.
Affiliations
CureVac (Germany) (DE)
Corresponding author
Heidenreich, Regina
Venue
Methods in Molecular Biology
Published
2016-12-17
Volume
1499
Pages
89-107
ISSN
  • 1064-3745 (ISSN-L)
  • 1940-6029
OpenAlex
W2564437942
Cited by
57
References
15
Citations by year
2026: 2 · 2025: 6 · 2024: 8 · 2023: 5 · 2022: 8 · 2021: 12 · 2020: 6 · 2019: 3 · 2018: 5 · 2017: 2
FWCI
4.10
Type
book chapter
Language
en
Open access
closed
Locations
  • Methods in molecular biology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Interference and Gene Delivery
  • Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
Keywords
mRNA vaccines, protamine, mRNA stabilization, immunogenicity, mRNA synthesis, mRNA purification
MeSH terms
Immunogenicity, Vaccine, Animals, RNA, Messenger, Vaccines, Mice

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