The study, led by Sheetij Dutta, from the Walter Reed Army Institute of Research, US, and his colleagues, focused on a protein called Apical Membrane Antigen-1 (AMA1) needed by the Plasmodium falciparum parasite to invade blood cells and cause disease.

Study results suggest that a cocktail of AMA1 proteins from only a few different strains can overcome major limitations of an earlier designed version of AMA1-based vaccines.

The challenge with the malaria parasite in general and its AMA1 surface protein in particular is that both exist as multiple strains, researchers said.

Using AMA1 in a vaccine readies the human immune system for subsequent encounters with the parasite but when such a vaccine was previously tested in humans, it was effective mostly against one particular P falciparum strain.

To explore the potential for a more broadly protective vaccine, the scientists tested different cocktails of AMA1 from different parasite strains for their ability to elicit a diverse range of antibodies that are active in parasite inhibition assays.

They confirmed that a cocktail of AMA1 proteins from three different parasite strains was better than one or two, and one they call Quadvax, which contained AMA1 proteins derived from four different strains, led to an antibody response that was broader than the sum of strain-specific antibodies elicited by the four individual strains.

Moreover, Quadvax-elicited antibodies inhibited a range of parasites, including many strains that were different from those in the Quadvax mix.

In different laboratory tests, Quadvax-induced antibodies inhibited the growth of 26 different parasite strains, and the scientists suggest that ‘the combination of four AMA1 variants in Quadvax may be sufficient to overcome global AMA1 diversity’.

Besides varying a lot from strain to strain, AMA1 also contains less variable (conserved) exposed parts (so-called epitopes) on its surface.

The researchers found that vaccination with Quadvax yielded not only antibodies against the variable epitopes, but also against more conserved epitopes of the AMA1 protein.

Such antibodies were not seen when using individual strains for immunisation but Quadvax appeared to enhance the immunogenicity—the ability to provoke an antibody response—of these conserved parts of the protein.

Since the epitopes are identical across strains, the resulting antibodies are broadly active rather than strain-specific, researchers said.

The study was published in the journal PLOS Pathogens.


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