Development of a Virosomal RSV Vaccine Containing 3D-PHAD® Adjuvant: Formulation, Composition, and Long-Term
J Lederhofer1, J van Lent2, F Bhoelan3
1University Medical Centre Groningen, Department of Medical Microbiology, University of Groningen, Groningen, The Netherlands.
Stable virosomes were formulated for Respiratory Syncytial Virus (RSV) vaccines using the 3D-PHAD® adjuvant. These stable virosomes show potential for effective vaccine development.
Area of Science:
- Vaccinology
- Virology
- Nanotechnology
Background:
- Respiratory Syncytial Virus (RSV) is a major cause of respiratory illness in infants and older adults.
- Current RSV vaccines are limited, necessitating the development of novel vaccine candidates.
- Virosomes are promising vaccine delivery systems that can incorporate viral antigens and adjuvants.
Purpose of the Study:
- To characterize virosomes formulated with a synthetic monophosphoryl lipid A, 3D-PHAD® adjuvant, for potential use as RSV vaccines.
- To evaluate the stability and immunogenicity of these adjuvanted virosomes in preclinical development.
Main Methods:
- Virosomes were prepared using different methods involving lipid films, viral membranes, and the adjuvant 3D-PHAD®.
- Characterization included cryo-electron microscopy, single particle tracking (SPT), and dynamic light scattering.
- Stability was assessed over 300 days, and antibody titers were measured.
Main Results:
- Virosomes incorporated viral glycoproteins G and F, along with lipids and the 3D-PHAD® adjuvant.
- Single particle tracking revealed stable virosome size, while dynamic light scattering indicated small aggregates.
- Enhanced 3D-PHAD® incorporation was achieved using DCPC-solubilized or DMSO-dissolved adjuvant, leading to comparable antibody titers.
Conclusions:
- Stable 3D-PHAD® adjuvanted RSV virosomes can be successfully formulated.
- These findings support the further development of virosome-based RSV vaccines.
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