Exciting new vaccine targets killer disease TB
Reported in the ‘Journal of Medicinal Chemistry’, the early-stage vaccine was shown to provide substantial protection against TB in a pre-clinical laboratory setting.
“Tuberculosis is a huge world-wide health problem. It’s caused by a bacteria that infects the lungs after it’s inhaled, is contagious and results in approximately 1.6 million deaths per year globally,” said Dr Anneliese Ashhurst, co-lead author of the reported study and affiliated with both the Centenary Institute and the University of Sydney.
The research program targeting the deadly disease has currently taken over five years of effort to implement. During that time Dr Ashhurst and a team of scientists have created the advanced synthetic TB vaccine and have now demonstrated its effectiveness using mouse models.
“Two peptides (small proteins) which are normally found in tuberculosis bacteria were synthesized and then bound extremely tightly to an adjuvant (a stimulant) that was able to kick-start the immune response in the lungs,” said Dr Ashhurst.
“We were then able to show that when this vaccine was inhaled into the lungs, it stimulated the type of T cells known to protect against TB. Importantly, we then demonstrated that this type of vaccine could successfully protect against experimental airborne TB infection,” she said.
Professor Warwick Britton, Head of the Centenary Institute Tuberculosis Research Program and co-senior researcher on the project with Professor Richard Payne, School of Chemistry, University of Sydney, emphasized the importance of the work being done.
“There currently exists only one lone vaccine for TB (known as BCG) and this is only effective in reducing the risk of disease for infants,” said Professor Britton.
“It fails to prevent infection or provide long term protection in older individuals and it isn’t considered suitable for use in individuals with an impaired immune system. More effective vaccines are urgently required to save lives,” he said.
Read the full media release here.