Advances in mRNA Vaccines for Infectious Diseases
Abstract
Vaccines play a crucial role in safeguarding global health. While traditional vaccine methods have been effective against various bacterial and viral diseases, there are instances where they have fallen short. This includes persistent infections, rapidly mutating pathogens with high genetic variability, intricate viral antigens, and emerging diseases. However, innovative technologies like nucleic acid vaccines have the potential to revolutionize vaccine development by overcoming these limitations. Messenger RNA (mRNA) vaccines have emerged as a promising platform for the prevention of infectious diseases.
Unlike conventional vaccines that rely on attenuated pathogens or recombinant proteins, mRNA vaccines use a synthetic RNA molecule encoding an antigen of interest. Once delivered into host cells, the mRNA is translated into the antigenic protein, which subsequently triggers immune responses. In this article, we discuss about the basic structure of mRNA vaccines, their mechanisms of immune activation, delivery technologies such as lipid nanoparticles, manufacturing strategies, and ongoing clinical developments. The potential benefits of mRNA vaccine platforms are substantial, but challenges related to stability, delivery efficiency, and global accessibility remain important considerations.
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References
Abbas, A. K., Lichtman, A. H., & Pillai, S. (2021). Cellular and molecular immunology (10th ed.). Elsevier.
Andre, F. E., Booy, R., Bock, H. L., Clemens, J., Datta, S. K., John, T. J., ... & Schmitt, H. J. (2008). Vaccination greatly reduces disease, disability, death and inequity worldwide. Bulletin of the World Health Organization, 86, 140–146.
Baden, L. R., El Sahly, H. M., Essink, B., Kotloff, K., Frey, S., Novak, R., ... & Zaks, T. (2021). Efficacy and safety of the mRNA-1273 SARS-CoV-2 vaccine. New England Journal of Medicine, 384(5), 403–416.
Barouch, D. H., & Picker, L. J. (2014). Novel vaccine vectors for HIV-1. Nature Reviews Microbiology, 12, 765–771.
Bartok, E., & Hartmann, G. (2020). Immune sensing mechanisms that discriminate self from altered self and foreign nucleic acids. Immunity, 53, 54–67.
Dimitrov, J. D., & Lacroix-Desmazes, S. (2020). Non-canonical functions of antibodies. Trends in Immunology, 41, 379–393.
Dolgin, E. (2021). The tangled history of mRNA vaccines. Nature, 597(7876), 318–324.
Ertl, H. C. (2016). Viral vectors as vaccine carriers. Current Opinion in Virology, 21, 1–8.
Folegatti, P. M., Ewer, K. J., Aley, P. K., Angus, B., Becker, S., Belij-Rammerstorfer, S., ... & Pollard, A. J. (2020). Safety and immunogenicity of the ChAdOx1 nCoV-19 vaccine. The Lancet, 396, 467–478.
Hou, X., Zaks, T., Langer, R., & Dong, Y. (2021). Lipid nanoparticles for mRNA delivery. Nature Reviews Materials, 6, 1078–1094.
Jackson, L. A., Anderson, E. J., Rouphael, N. G., Roberts, P. C., Makhene, M., Coler, R. N., ... & Beigel, J. H. (2020). An mRNA vaccine against SARS-CoV-2 — preliminary report. New England Journal of Medicine, 383, 1920–1931.
Karikó, K., Buckstein, M., Ni, H., & Weissman, D. (2005). Suppression of RNA recognition by Toll-like receptors through nucleoside modification. Immunity, 23(2), 165–175.
Lu, L. L., Suscovich, T. J., Fortune, S. M., & Alter, G. (2018). Beyond binding: antibody effector functions in infectious diseases. Nature Reviews Immunology, 18, 46–61.
Mulligan, M. J., Lyke, K. E., Kitchin, N., Absalon, J., Gurtman, A., Lockhart, S., ... & Dormitzer, P. R. (2020). Phase I/II study of COVID-19 RNA vaccine BNT162b1. Nature, 586, 589–593.
Pardi, N., Hogan, M. J., Porter, F. W., & Weissman, D. (2018). mRNA vaccines — a new era in vaccinology. Nature Reviews Drug Discovery, 17, 261–279.
Plotkin, S. (2014). History of vaccination. Proceedings of the National Academy of Sciences, 111(34), 12283–12287.
Polack, F. P., Thomas, S. J., Kitchin, N., Absalon, J., Gurtman, A., Lockhart, S., ... & Gruber, W. C. (2020). Safety and efficacy of the BNT162b2 mRNA Covid-19 vaccine. New England Journal of Medicine, 383, 2603–2615.
Sadoff, J., Le Gars, M., Shukarev, G., Heerwegh, D., Truyers, C., de Groot, A. M., ... & Schuitemaker, H. (2020). Interim results of a phase 1–2a trial of Ad26.COV2.S Covid-19 vaccine. New England Journal of Medicine, 384, 1824–1835.
Sahin, U., Derhovanessian, E., Miller, M., et al. (2017). Personalized RNA mutanome vaccines mobilize poly-specific therapeutic immunity against cancer. Nature, 547, 222–226.
Sahin, U., Karikó, K., & Türeci, Ö. (2014). mRNA-based therapeutics—developing a new class of drugs. Nature Reviews Drug Discovery, 13, 759–780.
Schlake, T., Thess, A., Fotin-Mleczek, M., & Kallen, K. J. (2012). Developing mRNA-vaccine technologies. RNA Biology, 9(11), 1319–1330.
Verbeke, R., Lentacker, I., De Smedt, S. C., & Dewitte, H. (2019). Three decades of messenger RNA vaccine development. Nano Today, 28, 100766.
Wolff, J. A., Malone, R. W., Williams, P., Chong, W., Acsadi, G., Jani, A., & Felgner, P. L. (1990). Direct gene transfer into mouse muscle in vivo. Science, 247, 1465–1468.
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