Malaria affects 300 million people each year. One million die, mostly children in sub-Saharan Africa.There are many malaria parasites. Plasmodium falciparum is the most deadly and researchers at the Sanger Institute acknowledge it as a "very complex and cunning foe". It is exceptionally good at evading and bamboozling the immune system. Within five minutes of being bitten by a malaria-carrying mosquito, the parasite is already hiding inside the liver.
The parasite reproduces in the red blood cells ( actual infected cell on the right)
It then emerges from the liver at a different stage in its life cycle and infects red blood cells, where it starts reproducing. The human immune system struggles to build up resistance to malaria and researchers have struggled in the laboratory.
There is still no approved vaccine against malaria. Large scale trials of the most advanced prototype - RTS,S - showed it halved the risk of getting malaria. This study looked at the moment the parasite infected a red blood cell. They were looking for proteins on the surface of Plasmodium and red blood cells which were necessary for the parasite to identify its target and invade.
The team at the Sanger Institute discovered that "basigin", a receptor on the surface on red blood cells, and "PfRh5", a protein on the parasite, were crucial. In all strains of Plasmodium falciparum tested so far, interrupting the link protected the blood cells from attack.
One of the researchers, Dr Julian Rayner, said: "We were able to completely block invasion using multiple different methods, using antibodies targeting this interaction we could stop all invasion of red blood cells. The plan is to develop a vaccine which will prime the immune system to attack PfRh5 on the parasite
Fellow researcher Dr Gavin Wright said a vaccine would have great potential as the target was so essential. "As a starting point for developing a vaccine you couldn't hope for better," he said.
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