The first data from clinical trials of Moderna’s mRNA-based seasonal flu vaccine, released by the company Friday morning, were underwhelming — a finding that shows gene-based vaccines might not be a fix for all the problems with vaccine development.
The overwhelming success of the mRNA COVID-19 vaccines, made by Moderna and Pfizer / BioNTech, supercharged interest in that strategy for developing shots. The shots inject people with tiny snippets of the gene for a virus, which the body builds and then uses to learn how to fight the virus.
Current flu shots contain inactivated copies of the influenza virus. mRNA vaccines are faster to design and produce because manufacturers don’t have to grow copies of the virus, which is why experts have for years seen them as the future of vaccines.
Moderna launched a clinical trial of an mRNA seasonal flu vaccine this summer, hoping to capture the same success as it did with its COVID-19 vaccine. Typically, seasonal flu shots are around 40 to 60 percent effective, and pharmaceutical companies want to make that better. Three other companies are also working on mRNA flu shots.
Moderna released its first results during an investor phone call and presented slides showing that the mRNA flu shots did generate antibodies — but the levels of those antibodies weren’t higher than those for other flu shots already on the market. They also had more side effects than existing shots.
The findings don’t necessarily mean that mRNA flu shots aren’t any better than what we have now. Because mRNA vaccines are faster to design and make, the shots don’t have to be developed as far in advance. Companies may not have to do as much guesswork around what strain of the flu to target them against each year because they can wait to make the shots until they see what strains are circulating.
And as far as efficacy goes, there’s still a lot more data to collect: Moderna is preparing to conduct larger trials that would test how well the shots actually keep people from getting sick in the real world (not just testing antibody levels)..
Still, this early data shows that the immune system is tricky and that mRNA vaccines probably aren’t an easy shortcut for stopping a virus as persistent as the flu. More studies will be needed to figure out if there is a specific benefit to using mRNA vaccines to fight the flu, wrote chemist and writer Derek Lowe in Science. But it’s not a sure thing.
Source: Moderna data shows mRNA isn’t a quick fix for the flu vaccine – The Verge
.
More contents:
- Non-viral COVID-19 vaccine delivery systems”. Advanced Drug Delivery Reviews. 169: 137–51. doi:10.1016/j.addr.2020.12.008. PMC 7744276. PMID 33340620.
- Delivering the Messenger: Advances in Technologies for Therapeutic mRNA Delivery”. Mol Ther. 27 (4): 710–28. doi:10.1016/j.ymthe.2019.02.012. PMC 6453548. PMID 30846391.
- “Three decades of messenger RNA vaccine development”. Nano Today. 28: 100766. doi:10.1016/j.nantod.2019.100766. hdl:1854/LU-8628303. S2CID 202221207.
- mRNA vaccines — a new era in vaccinology”. Nature Reviews Drug Discovery. 17 (4): 261–279. doi:10.1038/nrd.2017.243. ISSN 1474-1784. PMC 5906799. PMID 29326426.
- RNA vaccines: an introduction”. University of Cambridge. Retrieved 18 November 2020.
- Addressing the Cold Reality of mRNA Vaccine Stability”. Journal of Pharmaceutical Sciences. 110 (3): 997–1001. doi:10.1016/j.xphs.2020.12.006. PMC 7834447. PMID 33321139.
- “Mexico to start late-stage clinical trial for China’s mRNA COVID-19 vaccine”. Reuters. 11 May 2021. Retrieved 19 August 2021.
- “UK authorises Pfizer/BioNTech COVID-19 vaccine” (Press release). Department of Health and Social Care. 2 December 2020.
- UK approves Pfizer/BioNTech Covid vaccine for rollout next week”. The Guardian. Retrieved 2 December 2020.
- “Conditions of Authorisation for Pfizer/BioNTech COVID-19 Vaccine” (Decision). Medicines & Healthcare Products Regulatory Agency. 8 December 2020.
- “FDA Takes Key Action in Fight Against COVID-19 By Issuing Emergency Use Authorization for First COVID-19 Vaccine”. U.S. Food and Drug Administration (FDA) (Press release). 11 December 2020. Retrieved 6 February 2021.
- The Advisory Committee on Immunization Practices’ Interim Recommendation for Use of Pfizer-BioNTech COVID-19 Vaccine – United States, December 2020″ (PDF). MMWR Morb Mortal Wkly Rep. 69 (50): 1922–24. doi:10.15585/mmwr.mm6950e2. PMC 7745957. PMID 33332292.
- “FDA Takes Additional Action in Fight Against COVID-19 By Issuing Emergency Use Authorization for Second COVID-19 Vaccine”. U.S. Food and Drug Administration (FDA) (Press release). 18 December 2020.
- The Advisory Committee on Immunization Practices’ Interim Recommendation for Use of Moderna COVID-19 Vaccine – United States, December 2020″ (PDF). MMWR Morb Mortal Wkly Rep. 69 (5152): 1653–56. doi:10.15585/mmwr.mm695152e1. PMID 33382675. S2CID 229945697.
- mRNA Vaccine Era-Mechanisms, Drug Platform and Clinical Prospection”. International Journal of Molecular Sciences. 21 (18): 6582. doi:10.3390/ijms21186582. PMC 7554980. PMID 32916818.
Initiation of cationic lipid-mediated mrna transfection; Concept
- Malone RW, Felgner PL, Verma IM (August 1989).
- Cationic liposome-mediated RNA transfection”. Proceedings of the National Academy of Sciences of the United States of America. 86 (16): 6077–81. “
- After COVID-19 successes, researchers push to develop mRNA vaccines for other diseases”. Nature. Retrieved 31 July 2021.Xu S, Yang K, Li R, Zhang L (September 2020).
- mRNA Vaccine Era-Mechanisms, Drug Platform and Clinical Prospection”