Bacterial Outer Membrane Vesicles (OMVs)-based Dual Vaccine for Influenza A H1N1 Virus and MERS-CoV.
Mahmoud M ShehataAhmed MostafaLisa TeubnerSara H MahmoudAhmed M KandeilRabeh ElsheshenyRenate FrantzLuigi La PietraStephan PleschkaAhmed OsmanGhazi KayaliTrinad ChakrabortyMohamed A AliMobarak Abu MraheilPublished in: Vaccines (2019)
Vaccination is the most functional medical intervention to prophylactically control severe diseases caused by human-to-human or animal-to-human transmissible viral pathogens. Annually, seasonal influenza epidemics attack human populations leading to 290-650 thousand deaths/year worldwide. Recently, a novel Middle East Respiratory Syndrome Coronavirus emerged. Together, those two viruses present a significant public health burden in areas where they circulate. Herein, we generated a bacterial outer membrane vesicles (OMVs)-based vaccine presenting the antigenic stable chimeric fusion protein of the H1-type haemagglutinin (HA) of the pandemic influenza A virus (H1N1) strain from 2009 (H1N1pdm09) and the receptor binding domain (RBD) of the Middle East Respiratory Syndrome Coronavirus (MERS-CoV) (OMVs-H1/RBD). Our results showed that the chimeric antigen could induce specific neutralizing antibodies against both strains leading to protection of immunized mice against H1N1pdm09 and efficient neutralization of MERS-CoV. This study demonstrate that OMVs-based vaccines presenting viral antigens provide a safe and reliable approach to protect against two different viral infections.
Keyphrases
- respiratory syndrome coronavirus
- sars cov
- coronavirus disease
- endothelial cells
- public health
- cell therapy
- healthcare
- escherichia coli
- pluripotent stem cells
- dendritic cells
- type diabetes
- metabolic syndrome
- stem cells
- early onset
- mesenchymal stem cells
- immune response
- zika virus
- skeletal muscle
- binding protein
- antimicrobial resistance
- bone marrow