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

Author:

Eberlein Valentina12,Ahrends Mareike23,Bayer Lea1,Finkensieper Julia12,Besecke Joana Kira24,Mansuroglu Yaser25,Standfest Bastian26,Lange Franziska12,Schopf Simone24,Thoma Martin26ORCID,Dressman Jennifer25,Hesse Christina23,Ulbert Sebastian12,Grunwald Thomas12

Affiliation:

1. Fraunhofer Institute for Cell Therapy and Immunology, 04103 Leipzig, Germany

2. Fraunhofer Cluster of Excellence Immune-Mediated Diseases CIMD, 60596 Frankfurt am Main, Germany

3. Fraunhofer Institute for Toxicology and Experimental Medicine, 30625 Hannover, Germany

4. Fraunhofer Institute for Organic Electronics, Electron Beam and Plasma Technology FEP, 01277 Dresden, Germany

5. Fraunhofer Institute for Translational Medicine and Pharmacology, 60596 Frankfurt, Germany

6. Fraunhofer Institute for Manufacturing Engineering and Automation, 70569 Stuttgart, Germany

Abstract

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.

Funder

Cluster of Excellence of the Fraunhofer Gesellschaft

Publisher

MDPI AG

Subject

Virology,Infectious Diseases

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