Researchers have developed a universal influenza vaccine targeting a protein common to all strains of influenza A that has safely produced an immune response in humans. If proven effective, the vaccine could eliminate the practice of creating a new flu vaccine annually to match predicted strains.

The results of the clinical trials, led by the University of Texas Medical Branch at Galveston in collaboration with VaxInnate, Cranbury, NJ, a biotechnology company, and funded with a $9.5 million grant from the Bill and Melinda Gates Foundation, appear in the journal Vaccine.

The vaccine candidate, VAX102, targets a protein known as M2e, found on the surface of the influenza A virus, that has remained relatively unchanged over the last century. VAX102 consists of four copies of M2e fused to the protein flagellin, a TLR5 ligand used as an adjuvant. The M2e antigen had been completely unchanged from 1918 until the recent pandemic, making it of interest to researchers searching for a target for the immune response to influenza that would be stable over many seasons.

Unlike traditional flu vaccines, which target antigens that change continuously, the prototype VAX102 represents a vaccine that would not require annual updates, an important barrier to influenza prevention throughout the world. The technology used to produce the candidate vaccine would eliminate many of the limitations of current influenza vaccines, including inefficiencies related to manufacturing—such as limited production capability and the inability to change the target antigen should the vaccine not match the circulating strains.

The clinical trials assessed the safety, tolerability, and immunogenicity—the induced immune response—of VAX102. Healthy adults ages 18 to 49 were randomly assigned to receive two doses of either vaccine or placebo. The two studies established the dose range for further study. Doses ranging from 0.03 to 10 µg were studied. Individuals at the highest doses had more systemic reactions; doses of 1 µg or less were safe. All vaccinated subjects showed some degree of antibody response, with a more than four-old increase noted in all groups by 14 days after the second dose of vaccine.

An important next step will be studies to determine the degree to which the vaccine may be effective against influenza infection. Future studies would also investigate the durability of the antibody response and more closely assess cytokine responses—proteins released as part of the immune response—in an effort to better understand, predict, and potentially prevent the adverse reactions noted at highest doses.

Pending results of future trials, VAX102 could be used as a stand-alone vaccine to prevent influenza A infection. Other possible strategies include use in conjunction with vaccines that target traditional influenza antigens, as a part of an approach to increase efficacy when infection occurs with mismatched strains.

According to the researchers, an influenza vaccine that can be produced rapidly and with great economies of scale, such as VAX102 through simple bacterial fermentation, allows for an entirely new approach to international influenza control. Further, because the M2e-based vaccine would not require annual updates, it could be useful to offer protection over multiple influenza seasons.

VAX102 also holds promise as an improved vaccine for the elderly. According to the researchers, the elderly, currently, aren’t afforded as much protection from the flu vaccine as younger individuals. VAX102 could benefit the elderly, affording them long-term protection through a booster strategy rather than higher doses of the vaccine each year.

Source: University of Texas Medical Branch at Galveston