Seqirus looks to next-gen mRNA for seasonal flu vaccine

Seqirus says it will look to build large-scale manufacturing capacity to support its sa-mRNA ambitions in the seasonal influenza space.

Dan Stanton, Managing editor

August 31, 2021

3 Min Read
Seqirus looks to next-gen mRNA for seasonal flu vaccine
Image: Stock Photo Secrets

Seqirus says it will look to build large-scale manufacturing capacity to support its self-amplifying messenger RNA (sa-mRNA) ambitions in the seasonal influenza space.

Seqirus has long had a leading role in the seasonal influenza space through its portfolio of products, including both egg-based and cell-based vaccine.

But now the firm is stepping up its efforts to develop a flu vaccine based on mRNA, launching a dedicated program to support development of its next-generation sa-mRNA platform with plans to set up scaled-up manufacturing capabilities.


Image: Stock Photo Secrets

“Across our global manufacturing network, Seqirus is expanding our capabilities to support increased supply of new and existing technologies,” Roberta Duncan, Seqirus’ newly appointed VP of mRNA Program Lead told BioProcess Insider.

“Building large scale capacity for sa-mRNA manufacturing is really an incremental addition to our current manufacturing network. We are currently considering a number of global locations to establish scaled manufacturing capabilities for our sa-mRNA platform technology. Additionally, at our sites across the US, UK, and Australia, we are currently working to implement new programs to support sa-mRNA vaccine development and manufacturing, specifically.”

Investment specifics were not divulged but both Seqirus and parent firm CSL are committed to advancing the technology, and “are well positioned to make strategic investments to accelerate the development of our next generation sa-mRNA influenza vaccine technology,” Duncan said.

Next-generation mRNA

mRNA has made the headlines over the past year due to its success in rolling out vaccines for COVID-19. Vaccines from Pfizer/BioNTech and Moderna have been administered to hundreds of millions, under Emergency Use Authorization (EUA), and this week the former received full US FDA approval.

But while the news from Seqirus has accelerated the industry’s research into mRNA vaccines, Duncan said Seqirus has been researching this technology’s viability in influenza vaccines for a number of years.

“Seqirus is currently undertaking pre-clinical work on an sa-mRNA-based flu vaccine, with plans to initiate human clinical trials in the second half of 2022,” she said, before explaining how sa-mRNA differs from ‘traditional’ mRNA.

“Traditional mRNA vaccines help protect against infectious diseases by giving instructions to cells in the body to make a protein, stimulating the immune response and leaving a blueprint to recognize and fight future infection,” she explained.

“Seqirus’ sa-mRNA is the next generation version of mRNA technology. Sa-mRNA also gives the body instructions to replicate mRNA, amplifying the amount of protein made, with the potential to use less antigen. In preclinical research, sa-mRNA technology demonstrated the potential to raise stronger cellular responses and generate significantly higher antibody titers at the same dose level as mRNA.”

Mixed technologies

While the firm is turning towards mRNA for future seasonal vaccines, Duncan said it will not replace other technologies and products both in development and on the market.

“We will continue to invest in our new technologies, as well as our existing technologies – egg, cell and adjuvant – to provide effective protection against influenza. We foresee multiple technologies will co-exist in the foreseeable future,” she said.

“Each of these technologies has demonstrated the ability to protect against influenza, and we see sa-mRNA as an important potential addition to our portfolio, not an instead.”

About the Author(s)

Dan Stanton

Managing editor

Journalist covering the international biopharmaceutical manufacturing and processing industries.

Founder and editor of Bioprocess Insider, a daily news offshoot of publication Bioprocess International, with expertise in the pharmaceutical and healthcare sectors, in particular, the following niches: CROs, CDMOs, M&A, IPOs, biotech, bioprocessing methods and equipment, drug delivery, regulatory affairs and business development.

From London, UK originally but currently based in Montpellier, France through a round-a-bout adventure that has seen me live and work in Leeds (UK), London, New Zealand, and China.

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