show that future malaria vaccines may be most effective if they target multiple parasite factors.
‘Five new targets for malaria could be paired in different combinations to develop an effective vaccine for the disease.’
Nearly half of the world's population is at risk of malaria and more than 200 million people are infected each year. The disease caused the deaths of almost half a million people globally in 2015.
Despite a large number of deaths, there is no highly effective vaccine currently available for malaria. Over the last 50 years, most attempts to develop vaccines have only focused on single targets.
In the new study, scientists have discovered five targets for future malaria vaccine development, which they suggest should be targeted in combination. An effective vaccine is urgently needed due to an expanding problem of drug resistance in the parasite.
The team screened 29 potential targets that were all thought to play a role in the parasite's ability to invade human red blood cells. Red blood cell invasion is an essential step in the parasite's lifecycle and is a stage when the parasite is at its most vulnerable and exposed to the immune system.
Researchers raised rabbit antibodies against all 29 targets, then tested the antibodies against two different strains of the deadly Plasmodium falciparum
malaria, one from Africa and one from Asia. Of the 29 antibodies, the team discovered five that reduced the parasite's ability to invade red blood cells in both malaria strains.
Dr Gavin Wright, an author from the Wellcome Trust Sanger Institute, said: "Producing a successful vaccine against parasites is challenging because they are very complex organisms with many components, making it difficult to know which ones to target. By studying the parasite's genome and working backward, in a process known as reverse vaccinology, we have discovered five vaccine targets which, if combined, show promise for further development."
People naturally exposed to malaria can develop immunity over time. The team worked with collaborators in the US and Mali to see whether the five antibodies they identified were associated with natural protection against malaria in people.
Scientists found that alone, no single antibody gave protection against malaria in people. However, combinations of the antibodies did protect against the parasite.
To investigate what was happening at the cellular level, researchers used video microscopy to watch the parasite attempt to invade red blood cells with and without the presence of antibodies. The team discovered that the different antibodies were attacking the parasite at different steps as it invaded the red blood cell. Scientists found that pairing antibodies that each acted at different steps led to a more effective combination.
Professor Pietro Cicuta, an author from the University of Cambridge, said, "Using video microscopy, we were able to see the different antibodies attacking the parasite at various stages as it attempted to invade red blood cells. These results give insight into a new, synergistic view of vaccine development. We believe a new vaccine would be the most effective if it put roadblocks at several points along the parasite's path into the red blood cells."
Dr Julian Rayner, the lead author from the Wellcome Trust Sanger Institute, said, "This study was only possible due to the scale of studying multiple vaccine targets, and the huge collaborative effort. By bringing together multiple areas of expertise, from genomics to large field studies of patients in Mali, and down to advanced video microscopy observing individual parasites, we have discovered several new vaccine targets that warrant further investigation. It's a great example of collaborative international science and its potential impact.