Induction of resistance to Schistosoma mansoni in mice by chemotherapy: migration of schistosomula in primary and challenge infections.

The fate of 75Se-labelled schistosomula in mice treated at 24 h post-infection with either Ro 11-3128 or oxamniquine, compared to untreated controls, was followed by compressed organ autoradiography. No difference in the total percentage of schistosomula detected as foci was found between the three groups at each sampling time. However, the distribution of schistosomula was altered. In oxamniquine-treated mice there was a delayed migration from the skin relative to controls and fewer parasites in total appeared to reach the lungs. In Ro 11-3128 treated mice very few parasites left the skin. Ro 11-3128 treatment induces resistance to challenge whereas oxamniquine does not. The fate of challenge schistosomula in previously infected Ro 11-3128 treated mice was also compared to that in control mice. There was evidence for delayed or reduced migration from the skin of Ro 11-3128 treated mice. Significant death of challenge parasites occurred in the lungs, or post-lung sites in both control and treated mice. It was not possible to conclude that any of the late attrition was immune-dependent in the treated mice and the results appeared to indicate that a significant fraction of parasite death occurred at the skin stage.

Schistosoma mansoni: migration and attrition of irradiated and challenge schistosomula in the mouse.

The fate of irradiated, immunizing cercariae and challenge schistosomula was investigated in mice using a quantitative, histological technique which would appear to be more efficient in estimating parasite numbers in skin and lungs than does the tissue mincing and incubation recovery technique used previously by other workers. There was evidence for slight retardation of irradiated (20 krad.) parasite migration in skin, but death of schistosomula in the skin appeared negligible. It was observed that the majority of irradiated parasites remained in the lungs until at least day 21 after infection, and that most schistosomula observed at this time were dead. In mice immunized with irradiated cercariae there was no evidence of attrition of the challenge infection in the skin. The migration profile of challenge parasites in the lungs of immunized animals was not significantly different from that of normal parasites in the lungs of naive animals. Dead challenge parasites were observed in the lungs but their numbers were not considered great enough to account for the final attrition measured by perfusion. It is suggested that the remainder of the attrition of challenge schistosomula may occur in the systemic and/or hepatic portal circulation.