Mouse infection models are described that demonstrate reduction of egg
production in Schistosoma haematobium infections and both worm loss a
nd reduced fecundity in S. bovis infections. Neither phenomenum could
be shown in S. mansoni infected mice. The immunological basis for thes
e anti-adult responses was inferred by comparison with infections in T
-cell deprived mice and by serum transfer of the ability to reduce a S
. bovis worm burden into immunocompromised hosts. Vaccination with irr
adiation attenuated parasites was also shown to have consequences for
the adults of a challenge infection of S. haematobium and S. bovis spe
cifically. Prior vaccination resulted in an abrogation of the anti-fec
undity and adult worm elimination that occurred in non-vaccinated simi
larly infected mice. These models are being used to define the targets
and mechanisms involved in anti-adult attrition. A serological assay,
quantitation of a circulating antigen (CAA) has been assessed for its
ability to measure worm burdens of different species of schistosome i
n mice. This assay will be used to question whether anti-adult immunit
y contributes to the pattern of infection with S. mansoni and S. haema
tobium in man.