4.6 Article

Mucosal Application of a Low-Energy Electron Inactivated Respiratory Syncytial Virus Vaccine Shows Protective Efficacy in an Animal Model

Journal

VIRUSES-BASEL
Volume 15, Issue 9, Pages -

Publisher

MDPI
DOI: 10.3390/v15091846

Keywords

respiratory syncytial virus; RSV; mucosal vaccine; inactivated vaccine; low-energy electron irradiation; LEEI; PC formulation; PCLS

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RSV is a common cause of respiratory tract infections in the elderly and children. A recent study explored the use of a mucosal vaccine using low-energy electron irradiated RSV formulated with phosphatidylcholine-liposomes. The results showed no adverse effects and an efficient induction of antibodies in mice, indicating the potential of this vaccine in protecting against RSV.
Respiratory syncytial virus (RSV) is a leading cause of acute lower respiratory tract infections in the elderly and in children, associated with pediatric hospitalizations. Recently, first vaccines have been approved for people over 60 years of age applied by intramuscular injection. However, a vaccination route via mucosal application holds great potential in the protection against respiratory pathogens like RSV. Mucosal vaccines induce local immune responses, resulting in a fast and efficient elimination of respiratory viruses after natural infection. Therefore, a low-energy electron irradiated RSV (LEEI-RSV) formulated with phosphatidylcholine-liposomes (PC-LEEI-RSV) was tested ex vivo in precision cut lung slices (PCLSs) for adverse effects. The immunogenicity and protective efficacy in vivo were analyzed in an RSV challenge model after intranasal vaccination using a homologous prime-boost immunization regimen. No side effects of PC-LEEI-RSV in PCLS and an efficient antibody induction in vivo could be observed. In contrast to unformulated LEEI-RSV, the mucosal vaccination of mice with PC formulated LEEI-RSV showed a statistically significant reduction in viral load after challenge. These results are a proof-of-principle for the use of LEEI-inactivated viruses formulated with liposomes to be administered intranasally to induce a mucosal immunity that could also be adapted for other respiratory viruses.

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