THE EPOCH TIMES – Due to concerns about the H5N1 avian virus, which has been shown to spread to humans, the U.S. Food and Drug Administration (FDA) has proposed a new approach to pandemic vaccines.
At the Vaccines and Related Biological Products Advisory Committee meeting on Thursday, Jerry Weir, director of the FDA’s Division of Viral Products, asked the 11 committee members to discuss changes to the influenza vaccine strain change process.
Under the current plan, vaccines would be developed before a pandemic to target specific high-risk viruses.
These vaccines can be released if a pandemic occurs, assuming they are safe because they follow established manufacturing processes. New seasonal influenza vaccines have an established manufacturing process of being produced in eggs or in cell lines.
These vaccines would not need to undergo a clinical trial as they would be made to the same standard as seasonal influenza vaccines, and there is an assumed history of efficacy and safety for these vaccines for seasonal influenza, according to the FDA.
The new plan suggests that these vaccines should not only be used during a pandemic but also regularly updated.
Should an H5N1 pandemic break out, H5N1 vaccines would be made the same way as current seasonal influenza vaccines and updated accordingly. The new process would also allow the vaccines to be updated during the pandemic, depending on the circulating virus.
Todd Davis, acting chief of the Centers for Disease Control and Prevention’s (CDC) Virology, Surveillance, and Diagnosis Branch for virology surveillance, confirmed at the meeting that there is currently no evidence that the H5N1 avian virus has gained DNA mutations to cause infections in humans, though 16 cases have been reported in humans.
“We have not seen any mutations that would reduce susceptibility to antiviral drugs,” Davis added.
