US20260273040
2026-09-17
Human necessities
A61K39/145
The patent application discloses immunogenic compositions designed to protect against influenza and respiratory syncytial virus (RSV). These compositions include RNA molecules that encode influenza antigens, formulated in lipid nanoparticles (LNPs), and polypeptide antigens derived from RSV. The aim is to prevent illnesses caused by these viruses, addressing the limitations of traditional vaccines in terms of breadth and production speed, particularly during pandemics.
The compositions involve RNA vaccines encoding influenza antigens such as hemagglutinin (HA) and others like neuraminidase (NA) and nucleoprotein (NP). Additionally, these formulations include RSV polypeptides and/or polynucleotide molecules encoding RSV antigens. The RSV component focuses on the F protein, which is crucial for viral fusion and entry into host cells. The patent emphasizes the use of the pre-fusion form of the F protein, known for its stability and immunogenic potential.
Influenza viruses pose a challenge due to their antigenic variability, making it difficult for traditional vaccines to provide broad protection. RSV is a major cause of respiratory illness in infants and the elderly, with no approved vaccines currently available. The F protein of RSV, particularly in its pre-fusion form, is a primary target for vaccine development due to its role in viral entry and its recognition by neutralizing antibodies.
The disclosed compositions aim to improve immunogenic responses against both RSV and influenza. They incorporate RNA sequences encoding RSV F proteins or their variants, potentially stabilized in a pre-fusion state. These compositions may also include commercially available influenza vaccines, enhancing their protective efficacy. The application suggests using vaccines like Flublok, Fluzone, Arexvyโข, and ABRYSVOโข for comprehensive protection.
By combining RNA-based influenza antigens with RSV polypeptides, the disclosed compositions offer a promising approach to vaccine development. This dual-target strategy could lead to more effective prevention of respiratory infections, addressing the urgent need for vaccines that can be rapidly adapted and produced during pandemics. The focus on pre-fusion RSV F proteins highlights a strategic approach to enhance vaccine efficacy and durability.