A previous study performed in adolescents living in an area endemic for Sch
istosoma mansoni in Brazil has shown that a 37 kDa schistosome surface anti
gen is a selective target for antibodies in sera from those who were resist
ant to reinfection. This antigen was shown by molecular cloning to be the s
chistosome GAPDH. The aim of the present work was to assess whether peptide
s corresponding to GAPDH antigenic determinants could be used in a subunit
vaccine. Five B cell and two T cell epitopic regions were identified on Sm3
7-GAPDH. One of the B cell determinants (Sm37-5, aa 268-289) is highly anti
genic in human infections and antibody reactivity toward this determinant i
s associated with resistance to reinfection. Mice and rats immunized with S
m37-5 were partially protected against a challenge infection, indicating th
at this peptide can induce protective immunity. Analysis of Sm37-5 amino ac
id sequence indicated that this antigenic determinant is likely conserved a
mong other pathogenic strains of schistosome (S. haematobium, S. intercalat
um and S. japonicum), although it shows major amino acid differences with t
he corresponding human GAPDH sequence. All together these results indicate
that Sm37-5 should be considered as a candidate component for an anti-schis
tosome subunit vaccine. (C) 2000 Elsevier Science Ltd. All rights reserved.