December 6, 2018

“We’re excited about it.” – CSL talks up new flu vaccine

Melbourne Biomedical Precinct Partners, CSL Limited presented new real-world data showing that its cell-based quadrivalent influenza vaccine (QIVc) was 36.2 percent more effective than standard* egg-based quadrivalent vaccines (QIVe) in preventing influenza-like illnesses during the 2017/18 influenza season in the United States. This is likely due to the predominance of the H3N2 virus and its propensity for mutation when it is adapted for influenza vaccine production in chicken eggs. These observational data were presented today at the Canadian Immunisation Conference and also shared at CSL’s annual Research and Development briefing in Sydney.

The finding is based on an analysis of over one million (1,353,862) medical records for patients aged four years and above who received either a four-strain egg-based influenza vaccine or a four-strain cell-based influenza vaccine in a primary care setting during the 2017/18 influenza season in the United States. Analysing real-world data from electronic medical records is a new and important approach to understanding the effectiveness of influenza vaccines and their impact on health outcomes. These types of analyses are different from traditional randomised clinical trials which study clinical efficacy.

According to the US Centers for Disease Control1 the 2017/18 influenza season in the US was the worst in recent years with the H3N2 virus being associated with the majority of influenza infections. Research has shown that H3N2 viruses often undergo changes when they are grown in eggs2. When produced completely outside of the egg-based process, cell-based influenza vaccines avoid egg-adapted changes, which means they may offer a closer match and potentially improved protection compared to standard egg-based options in some seasons.3 4 5 6 7

QIVc was first licensed in the US in 2016 based on a study showing non-inferiority immune response to a three-strain cell-based influenza vaccine. Both cell-based products used in this study were produced using egg-based starting viruses8. The 2017/18 season was the first in which QIVc was manufactured using a cell-derived H3N2 starting virus, making this component of the vaccine exclusively cell-based. Seqirus is incorporating other cell-derived starting viruses into the production process for QIVc and has plans to conduct real-world studies over future seasons to help determine the full potential of the cell-based technology in preventing influenza.

“The real-world data, along with other emerging evidence, indicates that cell-based influenza vaccines may result in better influenza-related outcomes compared to standard egg-based vaccine options in some seasons, particularly those seasons characterised by egg-adapted changes,” said Gregg Sylvester, VP Medical Affairs, Seqirus. “We are greatly encouraged by the data and with increasing availability of our vaccine look forward to working with partners to generate additional data in future seasons.”

Developing new and better influenza vaccine technologies is a strategic priority for Seqirus, including further advancing current cell-based technology as well as adjuvants – or ‘immune boosters’ – to enhance the immune response of those particularly vulnerable to influenza such as children and the elderly.

While QIVc is currently only licensed in the US, the European regulatory agency (EMA) recently issued a positive recommendation for the vaccine, indicating formal approval in Europe by the end of 2018. Expansion into other markets is planned after that, including the submission of an application to the TGA in Australia in 2019.

Seqirus’ QIVc is manufactured in the company’s Holly Springs facility in North Carolina. The capacity of the plant to meet anticipated future demand for the vaccine has been greatly enhanced with approval by the FDA earlier in 2018 for important process improvements to the manufacturing process, and by the recently announced US$140 million plant expansion.

“The burden of influenza is a global healthcare concern, and Seqirus is committed to developing new and potentially better vaccines that help reduce the hundreds of thousands of deaths and severe illness caused every year by influenza. Since we acquired the cell-based technology just three years ago, we have increased vaccine production five-fold and introduced cell-derived starting viruses (rather than viruses that have been optimised to grow in eggs). These innovations together with other major investments into the Holly Springs facility will assist us to meet further global demand for the vaccine,” said CSL’s Chief Scientific Officer Professor Andrew Cuthbertson.

Influenza is a common, highly contagious infectious disease that can cause severe illness and life-threatening complications in many people. In Australia, the impacts of the 2017 season included high levels of absenteeism and a substantial burden on primary care and hospitals.9

“Vaccination is the best line of defence in reducing deaths and severe illness caused by influenza. Every flu season is different and it’s important that we stay one step ahead of influenza viruses through the development of more effective vaccines, better matched to the strains in circulation. This real-world data on cell-based vaccines is encouraging and will bring another welcome influenza vaccine option to Australia,” said Professor Terry Nolan AO, Head, Melbourne School of Population and Global Health. – ends –

*standard QIVe is non-adjuvanted with standard dose of antigen.

This article is sourced from Proud Precinct Partners, CSL

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