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mRNA Vaccines for Influenza: Hope for a Universal Vaccine?
Priscilla Omotara1, Wandi Zhu1, Bao-Zhong Wang2
1Center for Inflammation, Immunity and Infection, Institute for Biomedical Sciences, Georgia State University, 100 Piedmont Ave, Atlanta, GA, 30303, USA.
Abstract:
Seasonal influenza epidemics and pandemics remain a persistent public health threat. A universal influenza vaccine is urgently needed. Such a vaccine must accommodate rapid viral evolution, strain diversity-including types A and B and their many subtypes-and the complexities of human immune history and biases. Messenger RNA (mRNA)-formulated lipid-nanoparticles have evolved from an emergency pandemic vaccine experiment into a versatile vaccine platform. This technology has demonstrated potential to address several critical challenges in developing a universal influenza vaccine, including rapid strain updates, the production of high-valent formulations, and the ability to target conserved antigens that may induce broader and longer-lasting protection. This review summarizes recent studies and applications of multivalent antigen selection strategies and self-amplifying and circular RNA vaccine platforms to develop mRNA influenza vaccines to achieve vaccine universality, with an emphasis on immune responses against conserved targets. We also review the latest advances in generating long-term mucosal immunity against influenza through optimized mRNA delivery. Finally, we discuss practical considerations for correlates of protection, manufacturing, and accessibility, pioneering mRNA vaccine candidates heading to clinical trials, and milestones that define vaccine "universality."
Insights
Messenger RNA (mRNA) vaccines show promise for a universal influenza vaccine, overcoming viral evolution and strain diversity challenges. This approach targets conserved antigens for broader, longer-lasting protection against flu.
Area of Science:
- Immunology
- Vaccinology
- Molecular Biology
Background:
- Seasonal influenza poses a continuous global health risk, necessitating novel vaccine strategies.
- Current influenza vaccines require frequent updates due to rapid viral evolution and strain diversity.
- Existing vaccines face challenges in addressing all influenza types (A and B) and subtypes effectively.
Purpose of the Study:
- To review the potential of messenger RNA (mRNA) vaccine technology for developing a universal influenza vaccine.
- To explore strategies for creating broadly protective and long-lasting immunity against influenza viruses.
- To discuss advancements in mRNA vaccine platforms and delivery for influenza.
Main Methods:
- Review of recent studies on mRNA vaccine platforms, including self-amplifying and circular RNA.
- Analysis of multivalent antigen selection strategies for universal influenza vaccine development.
- Examination of optimized mRNA delivery systems for inducing mucosal immunity.
Main Results:
- mRNA lipid-nanoparticle technology offers a versatile platform for rapid vaccine updates and high-valent formulations.
- Targeting conserved influenza antigens with mRNA vaccines can induce broader and more durable immune responses.
- Advances in mRNA delivery show potential for generating long-term mucosal immunity.
Conclusions:
- mRNA technology is a promising candidate for achieving a universal influenza vaccine.
- Further research into antigen selection, delivery optimization, and manufacturing is crucial for clinical translation.
- Defining correlates of protection and ensuring accessibility are key milestones for universal influenza vaccine success.
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