» Articles » PMID: 33414790

RNA Vaccines: A Suitable Platform for Tackling Emerging Pandemics?

Overview
Journal Front Immunol
Date 2021 Jan 8
PMID 33414790
Citations 38
Authors
Affiliations
Soon will be listed here.
Abstract

The COVID-19 pandemic demonstrates the ongoing threat of pandemics caused by novel, previously unrecognized, or mutated pathogens with high transmissibility. Currently, vaccine development is too slow for vaccines to be used in the control of emerging pandemics. RNA-based vaccines might be suitable to meet this challenge. The use of an RNA-based delivery mechanism promises fast vaccine development, clinical approval, and production. The simplicity of transcription of mRNA suggests potential for fast, scalable, and low-cost manufacture. RNA vaccines are safe in theory and have shown acceptable tolerability in first clinical trials. Immunogenicity of SARS-CoV-2 mRNA vaccines in phase 1 trials looks promising, however induction of cellular immunity needs to be confirmed and optimized. Further optimization of RNA vaccine modification and formulation to this end is needed, which may also enable single injection regimens to be achievable. Self-amplifying RNA vaccines, which show high immunogenicity at low doses, might help to improve potency while keeping manufacturing costs low and speed high. With theoretical properties of RNA vaccines looking promising, their clinical efficacy is the key remaining question with regard to their suitability for tackling emerging pandemics. This question might be answered by ongoing efficacy trials of SARS-CoV-2 mRNA vaccines.

Citing Articles

Preclinical development of lyophilized self-replicating RNA vaccines for COVID-19 and malaria with improved long-term thermostability.

Gulati G, Simpson A, MacMillen Z, Krieger K, Sharma S, Erasmus J J Control Release. 2024; 377:81-92.

PMID: 39547422 PMC: 11663110. DOI: 10.1016/j.jconrel.2024.11.023.


A Lipid Nanoparticle-Formulated Self-Amplifying RNA Rift Valley Fever Vaccine Induces a Robust Humoral Immune Response in Mice.

Kitandwe P, Rogers P, Hu K, Nayebare O, Blakney A, McKay P Vaccines (Basel). 2024; 12(10).

PMID: 39460255 PMC: 11511412. DOI: 10.3390/vaccines12101088.


Advances in Dendritic-Cell-Based Vaccines against Respiratory Fungal Infections.

Kulkarni N, Nanjappa S Vaccines (Basel). 2024; 12(9).

PMID: 39340013 PMC: 11435842. DOI: 10.3390/vaccines12090981.


Rapidly Evolving SARS-CoV-2: A Brief Review Regarding the Variants and their Effects on Vaccine Efficacies.

Nawaz S, Janiad S, Fatima A, Saleem M, Fatima U, Ali A Infect Disord Drug Targets. 2024; 24(4):58-66.

PMID: 38178666 DOI: 10.2174/0118715265271109231129112515.


A duplex droplet digital PCR assay for absolute quantification and characterization of long self-amplifying RNA.

Casmil I, Huang C, Blakney A Sci Rep. 2023; 13(1):19050.

PMID: 37923834 PMC: 10624827. DOI: 10.1038/s41598-023-46314-6.


References
1.
Corbett K, Edwards D, Leist S, Abiona O, Boyoglu-Barnum S, Gillespie R . SARS-CoV-2 mRNA vaccine design enabled by prototype pathogen preparedness. Nature. 2020; 586(7830):567-571. PMC: 7581537. DOI: 10.1038/s41586-020-2622-0. View

2.
Blakney A, McKay P, Yus B, Aldon Y, Shattock R . Inside out: optimization of lipid nanoparticle formulations for exterior complexation and in vivo delivery of saRNA. Gene Ther. 2019; 26(9):363-372. PMC: 6760535. DOI: 10.1038/s41434-019-0095-2. View

3.
Feldman R, Fuhr R, Smolenov I, Ribeiro A, Panther L, Watson M . mRNA vaccines against H10N8 and H7N9 influenza viruses of pandemic potential are immunogenic and well tolerated in healthy adults in phase 1 randomized clinical trials. Vaccine. 2019; 37(25):3326-3334. DOI: 10.1016/j.vaccine.2019.04.074. View

4.
Alberer M, Gnad-Vogt U, Hong H, Mehr K, Backert L, Finak G . Safety and immunogenicity of a mRNA rabies vaccine in healthy adults: an open-label, non-randomised, prospective, first-in-human phase 1 clinical trial. Lancet. 2017; 390(10101):1511-1520. DOI: 10.1016/S0140-6736(17)31665-3. View

5.
Stitz L, Vogel A, Schnee M, Voss D, Rauch S, Mutzke T . A thermostable messenger RNA based vaccine against rabies. PLoS Negl Trop Dis. 2017; 11(12):e0006108. PMC: 5737050. DOI: 10.1371/journal.pntd.0006108. View