In previous studies it was shown that the recombinant molecule, r-Sm14, ind
uces high levels of protection against Schistosoma mansoni infection in two
outbred animal models and immune crossprotection against infection by Fasc
iola hepatica in Swiss outbred mice. r-Sm14 was derived from a living worm
extract, called SE, and is being developed as the molecular basis of an ant
i-helminth bivalent vaccine against the two parasites, for medical and vete
rinary application. Present data refer to SDS-PAGE and Western Blotting ana
lysis of four different preparations of S. mansoni adult worms focusing Sm1
4 identification. The extracts correspond to the initial fraction of the SE
extraction process, containing products released by living worms (SEi); SE
2, reextraction of adult worms in PBS; and SE of separated male and female
adult worms. In all extracts it was possible to detect the component of 14
kDa, that was recognized by specific anti-rSm14 antibody raised in rabbits.