Aug 2026· Vaccines· Vol 14, pp. 709· 0 citations· 49 references
Medicine
TL;DR
Whether mRNA-1010 represents an incremental advance in influenza vaccination or a potential transformative milestone in respiratory immunization is examined, while considering the continuing roles of alternative vaccine platforms in achieving optimal effectiveness, safety, and equitable global access.
Abstract
Seasonal influenza remains a major global public health challenge despite decades of vaccine development, underscoring the need for more effective and adaptable immunization strategies. The recently approved mRNA-1010 vaccine represents a promising advance by applying messenger RNA technology to a pathogen characterized by continuous antigenic drift. Recent Phase 3 clinical trials conducted in support of regulatory review have demonstrated robust immunogenicity and superior protective efficacy against seasonal influenza compared with standard influenza vaccines in adults aged 50 years and older. However, increased reactogenicity, particularly among younger adults, together with the need for continued post-marketing safety surveillance, highlights the balance between enhanced immune responses and tolerability. Beyond seasonal influenza, mRNA-1010 provides a foundation for next-generation respiratory vaccines, including combination formulations targeting influenza, SARS-CoV-2, and respiratory syncytial virus (RSV), while illustrating the broader potential of mRNA vaccine technology. At the same time, challenges related to manufacturing scalability, cost, cold-chain requirements, and global accessibility remain important considerations for widespread implementation. This perspective examines whether mRNA-1010 represents an incremental advance in influenza vaccination or a potential transformative milestone in respiratory immunization, while considering the continuing roles of alternative vaccine platforms in achieving optimal effectiveness, safety, and equitable global access.
Whether mRNA platforms offer incremental benefits over enhanced formulations (such as high-dose, adjuvanted, or recombinant vaccines), which are the preferred options in some countries for older adults, remains to be established.
A. Domnich, Andrea Orsi· Frontiers in Immunology· 0 citations
Promising multicomponent influenza-COVID-19 vaccine candidates currently being evaluated in clinical trials may represent an important advancement in adult immunization strategy, and a meaningful opportunity to strengthen protection against two of the most consequential respiratory pathogens worldwide.
W. Schaffner, S. Gravenstein, S. Kissler et al.· Vaccine· 0 citations
Background. Seasonal influenza remains one of the most persistent causes of preventable respiratory morbidity and mortality worldwide, and the egg-propagated inactivated vaccines that have anchored control efforts for eight decades deliver only moderate and highly variable protection. Messenger RNA (mRNA) technology, v...
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Lu-Yao Qin, Meng-Yi Zhang, Xiao-Yuan Liu et al.· bioRxiv· 0 citations
Dengue is among the fastest-growing mosquito-borne viral infections worldwide and continues to pose a major public health challenge because no approved antiviral treatment is available. As a result, vaccination has become a cornerstone of dengue prevention. Several vaccine candidates have progressed through clinical de...
Vydeti Mounika, E. Sirisha, Srikakulapu Balu et al.· International journal of med...· 0 citations
It is demonstrated that an integrated generation–selection strategy can enhance vaccine coverage across current and future A(H3N2) seasons and may be applicable to other influenza subtypes.
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