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Key molecule may bring malaria vaccine closer

Press Trust of India  |  Melbourne 

Scientists have discovered a key molecule that helps immune cells to find and kill microbes that infect the human liver, an advance that could bring malaria vaccine a step closer.

Malaria is a disease spread by mosquitoes that kills around 500,000 people every year, mainly in tropical countries in sub-Saharan and the South Pacific, researchers said.

The findings help answer a mystery about the work of T-cells, which are a type of immune cell that look for infection throughout the body, said lead researcher Hayley McNamara, a PhD scholar at The Australian National University (ANU).

"We know T-cells can protect against most infections, what we still do not fully understand is how these T-cells find the rare cells infected with viruses or parasites like malaria - a needle in a haystack problem if you like," McNamara said.

"In our research we have been able to see that some of the T-cells are specialists, able to patrol the liver hunting down infections like malaria parasites.

"We have found that without a key molecule called LFA-1, that cells do not work - they can not move quickly and can not kill malaria parasites effectively," said McNamara.

ANU Associate Professor Ian Cockburn said that because the T-cells were so effective at finding malaria parasites they could be a component of future vaccines.

"What we want to do is understand how to make a vaccine that induces these types of immune cells. There are vaccines in clinical trials that work by inducing antibodies, adding a T-cell component would create stronger immunity by arming different parts of the immune system," Cockburn said.

ANU researchers are currently working with collaborators in Australia and internationally to find a vaccine approach to make this type of T-cell.

The research was published in the journal Science Immunology.

(This story has not been edited by Business Standard staff and is auto-generated from a syndicated feed.)

First Published: Mon, March 20 2017. 12:48 IST