Schistosomiasis, the second major parasitic disease in the world after mala
ria, affects 200 million people. Vaccine strategies represent an essential
component of the control of this chronic debilitating disease where the dep
osition of millions of eggs in the tissues is the main cause of pathology.
Research developed in our laboratory over the last 20 years has led to the
identification of novel effector mechanisms, pointing for the first time to
the protective role of Th2 responses and of IgE antibodies now supported b
y seven studies in human populations. The identification and molecular clon
ing of a target antigen, a glutathione S-transferase ( G ST), h as made it
possible to demonstrate its vaccine potential in several animal species (ro
dents, cattle, primates) and to establish consistently the capacity of vacc
ination to reduce female worm fecundity and egg viability through the produ
ction of neutralizing antibodies (IgA and IgG). Following promising preclin
ical studies, clinical trials (phase I and II) have been undertaken using S
chistosoma haematobium GSI, Sh28GST. High titers of neutralizing antibodies
were produced (IgG3 and IgA) together with Th2 cytokines, consistently wit
h the concepts developed from experimental models. With these results we ar
e on the way towards a feasible approach of vaccine development against a m
ajor human parasitic disease. Copyright (C) 2001 S. Karger AG, Basel.