Abstract
Summary We have characterized various anti-schistosomular surface MoAbs previously shown to partially block in-vitro killing of schistosomula by human sera and eosinophils (Dunne et at. 1987). Immunodiffusion analysis showed that four IgM and one IgG3 MoAbs recognized periodate sensitive epitopes on the same molecular species present in schistosomular antigen but their patterns of reactivity with soluble egg antigen demonstrated that at least three distinct epitopes were involved. SDS-PAGE analysis showed the TgMs to react with 125I-labelled surface antigens of Mr 35 000-38 000 and Mr 20 000, and the IgG3 to react with an Mr 38 000 antigen. In spile of their effect in vitro, transfer of the IgM MoAbs at the time ofchallenge of mice vaccinated with irradiated cercariae or of mice injected with an unrelated (anti-Mr 16 000) protective MoAb failed to produce in-vivo blocking. Similarly, injection of Schistosoma mansoni eggs, prior infection with worms of one sex, or passive transfer of serum from single-sex infected mice failed to influence the resistance conferred by vaccination with irradiated cercariae.