Various formulations of the Plasmodium falciparum merozoite surface an
tigen, MSA-2, were made and tested in animals in order to select one f
or use in human vaccine trials. Recombinant constructs representing bo
th major allelic forms of MSA-2 were formulated with a range of adjuva
nts and used to immunize rabbits, mice and sheep. After immunization,
antibody responses obtained with the most potent adjuvants were at lea
st tenfold greater than responses obtained with the least potent adjuv
ant Alhydrogel, which was used as the reference standard, although its
lower potency indicated against its further use in clinical trials. B
ased on broadly similar results obtained with the three animal species
, several adjuvants, including the water-in-oil adjuvant Montanide ISA
720, the oil-in-water adjuvant SAF-1, and liposomes containing lipid
A formulated with Alhydrogel were demonstrated to. be potent and poten
tially suitable for the clinical evaluation of MSA-2 as a candidate ma
laria vaccine antigen. Of these, ISA 720 was selected for further tria
l. (C) 1997 Elsevier Science Ltd.