Split antigen vaccine proves effective - GSK

By Staff Writers
Thursday, 08 March, 2007

Pharma giant GlaxoSmithKline (GSK) has released clinical trial data from two new studies which show that its candidate pre-pandemic split antigen H5N1 vaccine provides a substantial level of cross-immunity against a 'drifted' (diverse) strain of H5N1.

GSK said it was hoped that the immune response elicited with this vaccine could help prime the immune system to rapidly respond against variants of the H5N1 strain and therefore protect the vaccinated population in the event of an H5N1 human pandemic.

In the first study presented at the Ninth International Symposium on Respiratory Viral Infections (ISRVI), data demonstrated GSK's proprietary adjuvanted candidate pre-pandemic vaccine, containing very low levels of the Vietnam H5N1 antigen (3.8µg), elicits a strong cross-immune neutralising antibody response in humans against the Indonesian strain of the virus.

The neutralising antibody seroconversion factor at Day 42 was shown to be 25 times greater when the vaccine contained the adjuvant system compared with that observed in the control group immunised with a non-adjuvanted vaccine (77.1% vs. < 3%).

GSK's proprietary adjuvant system also displays powerful antigen-sparing properties as the strong neutralising response in this study was obtained with only two doses of 3.8µg HA antigen administered three weeks apart, according to a company statement. This could mean, in effect, that by adding GSK's proprietary adjuvant system vaccine manufacturing capacity could be increased more than tenfold. The vaccine was shown to have an acceptable safety profile when compared to the control group. As expected, reactogenicity (injection site tenderness) was slightly higher in the vaccine group due to the use of the adjuvant system.

In a second study presented at ISRVI, the data showed that GSK's proprietary adjuvanted pre-pandemic vaccine could protect against two diverse H5N1 flu strains, again at very low levels of antigen. The in vivo data from the pre-clinical studies demonstrated that GSK's adjuvanted vaccine, containing the Vietnam H5N1 strain, was not only able to protect against challenge with the vaccine virus strain but it also provides 96% (22/23) cross-protection against a lethal challenge with the drifted Indonesia strain of H5N1, giving an additional boost to hopes that pre-pandemic vaccination is a viable strategy for inclusion in pandemic preparedness plans.

"The data confirm that our pre-pandemic influenza vaccine has the ability to recognise and kill an H5N1 strain that is different to the one contained in the vaccine," Jean Stephenne, president of GlaxoSmithKline Biologicals, the vaccine division of GSK, said. "This means that proactive administration of our pre-pandemic vaccine before or just after the start of the pandemic could help to substantially slow down the spread of disease."

Source: GlaxoSmithKline

Related News

TGA approves first treatment for geographic atrophy

Australia has become the first country outside of the United States to approve the use of the...

Damaged RNA, not DNA, revealed as main cause of acute sunburn

Sunburn has traditionally been attributed to UV-induced DNA damage, but it turns out that this is...

Multi-ethnic studies identify new genes for depression

Two international studies have revealed hundreds of previously unknown genetic links to...


  • All content Copyright © 2025 Westwick-Farrow Pty Ltd