A new universal flu vaccine constructed with key parts of the influenza virus offers broad cross protection against different strains and subtypes of influenza A viruses in young and aged populations, according to a new study by researchers in the Institute for Biomedical Sciences at Georgia State University.
The researchers developed the universal flu vaccine by genetically linking two highly conserved (relatively unchanged over time) portions of the virus – the extracellular domain of matrix 2 (M2e) and the stalk protein found in influenza A H3N2 viruses. The findings, published in the journal npj Vaccines, show that M2e-stalk protein vaccination induced broad protection against different influenza virus strains and subtypes by universal vaccine-mediated immunity in adult and aged mice.
Scientists have faced obstacles in the development of effective vaccines for influenza viruses because the head portion of the influenza virus is constantly changing. When comparing the H1N1 and H3N2 influenza A viruses, particular challenges exist in H3N2 subtypes because of stalk mutations in circulating strains and the unstable structure of stalk proteins for H3N2 viruses. These drawbacks have been difficult to overcome in developing effective H3 stalk-based vaccines.
Vaccine effectiveness against H3N2 was low during the past decade, only about 33 percent, and dropped to 6 percent during the 2014-2015 flu season. New mutations of H3N2 variants emerged with increased virulence. Also, the outbreak of H7N9, another influenza A subtype, caused concern for potential pandemics. Therefore, developing an effective vaccine to protect against these viruses is a high priority.
The study found this novel M2e-stalk protein vaccine induced M2e and stalk-specific Immunoglobulin G (IgG) antibodies that recognized antigenically diverse influenza viral antigens on virus particles and on the infected cell surface. In addition, the vaccine stimulated protective cellular T cell immunity and effective lung influenza viral clearance in mice.
Co-authors of the study include Jeeva Subbiah (first author), Judy Oh, Ki-Hye Kim, Chong-Hyun Shin, Bo Ryoung Park, Noopur Bhatnagar, Bao-Zhong Wang and Sang-Moo Kang of the Institute for Biomedical Sciences at Georgia State; and Baik-Lin Seong of the College of Medicine and the Vaccine Innovative Technology Alliance (VITAL)-Korea at Yonsei University in the Republic of Korea.
Linda Bernstein, Pharm.D.Peer