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American Focus > Blog > Health and Wellness > NIH use of old vaccine method for universal flu vaccine questioned
Health and Wellness

NIH use of old vaccine method for universal flu vaccine questioned

Last updated: May 3, 2025 1:29 pm
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NIH use of old vaccine method for universal flu vaccine questioned
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The recent announcement of the Department of Health and Human Services investing half-a-billion dollars into a National Institutes of Health project to develop a vaccine platform for potential pandemic-triggering pathogens has sparked a mixed reaction among scientists in the field of vaccinology.

While the news of continued investment in efforts to develop vaccines that could mitigate the impact of future pandemics was generally well-received, the choice to focus on using whole killed viruses as the basis for these vaccines raised concerns among some experts. This approach, which dates back to the 1950s when Jonas Salk created the first polio vaccine, was criticized by scientists for being outdated and not aligned with more modern vaccine production processes.

Several scientists expressed confusion and disappointment over the decision to invest heavily in a technology that has been surpassed by newer, more efficient methods. Some likened the move to a step backward in vaccine development. Critics of the plan questioned the efficacy of using whole killed viruses as a basis for vaccines and raised concerns about the lack of innovation in the chosen approach.

The project, led by in-house scientists Matthew Memoli and Jeffery Taubenberger, did not undergo the usual peer-reviewed appraisal process that external researchers typically go through when seeking NIH funding. This led to criticisms of the funding allocation process, with some scientists labeling it as “incestuous.”

Stanley Plotkin, a renowned vaccines researcher, expressed doubts about the vetting process and the adequacy of the allocated funding for the project. He emphasized the need for a better influenza vaccine but questioned whether the Generation Gold Standard project would achieve that goal.

Initial results from a Phase 1 trial of the NIH group’s universal flu vaccine, which only targets four subtypes of flu, received a lukewarm response from scientists who reviewed the data. While the injected version of the vaccine showed moderate antibody responses, the intranasal version did not perform as well.

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Despite the skepticism surrounding the project, the Generation Gold Standard aims to develop a vaccine platform using whole killed viruses to protect against pandemic-prone viruses. While this method has historical precedent in early vaccine production, the evolution of vaccine design has led to newer, more efficient approaches that are favored by many in the scientific community.

In conclusion, the decision to invest in a vaccine platform based on whole killed viruses has sparked debate among scientists, with some questioning the efficacy and innovation of this approach. As the project progresses, it will be important to address these concerns and ensure that the chosen method aligns with current best practices in vaccine development. The push for newer technologies in vaccine development has gained momentum in recent years, with researchers and scientists striving to create more effective and efficient vaccines to combat a range of infectious diseases. A recent project announced by Director Jay Bhattacharya has been hailed as a “paradigm shift” in vaccine development, aiming to extend vaccine protection beyond strain-specific limits and prepare for future viral threats using traditional vaccine technology brought into the 21st century.

This ambitious project envisions the development of a universal flu vaccine that could protect against multiple strains of influenza, as well as vaccines that could target a variety of coronaviruses and other disease threats. It is projected that a universal flu vaccine could be approved as early as 2029, a significant breakthrough in the field of vaccine research.

However, not everyone is convinced of the feasibility and effectiveness of this new approach. Some scientists have raised concerns about the lack of clarity surrounding the project’s goals and objectives. Additionally, the reallocation of funding from other vaccine development programs, such as Project NextGen, has sparked criticism and skepticism among the scientific community.

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One of the key concerns raised by scientists is the potential shift away from mRNA vaccines, which have played a crucial role in the response to the Covid-19 pandemic. While the project aims to develop multivalent inactivated influenza vaccines, experts emphasize the importance of continuing to explore and fund other promising vaccine platforms, such as mRNA vaccines that can target multiple influenza antigens simultaneously.

The controversy surrounding the project also highlights political considerations, with concerns raised about the unpopularity of mRNA vaccines among certain political groups. This has led to a review of funding for mRNA vaccine manufacturers, raising questions about the future of this innovative vaccine technology.

Despite the ongoing debates and controversies, the need for newer technologies in vaccine development remains paramount. The rapid production and scalability of mRNA vaccines have proven to be invaluable during public health emergencies, such as the Covid-19 pandemic. While traditional vaccine production methods have their benefits, newer technologies offer the promise of faster and more effective vaccine development, ultimately improving our ability to respond to emerging infectious diseases. As the scientific community continues to explore and innovate in the field of vaccine development, it is essential to consider a diverse range of technologies to ensure comprehensive and effective protection against a wide range of infectious diseases. The newer version of the vaccine, although made in a different way, has shown to be less protective compared to the former whole cell version. However, it does not cause the same rates of high fever, febrile seizures, prolonged crying, and injection site reactions that were commonly seen with the previous version. This trade-off between efficacy and safety is a key consideration in vaccine development.

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Dr. Garcia-Sastre, a member of the Generation Gold Standard team, highlighted that the newer vaccines are more immunogenic and likely better at providing protection. However, he also mentioned that an excessive immune response can lead to adverse events in some individuals. This delicate balance between effectiveness and safety is crucial in vaccine design.

One of the innovative approaches being explored by the Generation Gold Standard team is the development of intranasal vaccines using whole viruses. Dr. Garcia-Sastre emphasized the need for careful monitoring of potential adverse events, such as Bell’s palsy, which has been linked to a previous intranasal influenza vaccine that is no longer on the market. It is important to note that the intranasal approach with a reactogenic vaccine requires thorough evaluation for safety.

As advancements in vaccine technology continue, researchers must prioritize both efficacy and safety in vaccine development. The goal is to create vaccines that not only provide strong protection against diseases but also minimize the risk of adverse reactions. By carefully balancing these factors, the Generation Gold Standard team aims to develop vaccines that are both effective and safe for the population.

TAGGED:FlumethodNIHQuestionedUniversalvaccine
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