Successful vaccine development for schistosomiasis has been hindered by a l
ack of consensus on the type of immune response that would provide maximum
levels of protective immunity and incomplete knowledge of the key antiparas
ite effector mechanisms. Many vaccine studies conducted in mice support typ
e-1-cytokine-mediated effector mechanisms, while acquired resistance in hum
ans correlates with type-2-cytokine-mediated responses. However, recent dat
a from cytokine-knockout mice suggest that choosing between these opposing
pathways may be less important than previously hypothesized, as discussed h
ere by Thomas Wynn and Karl Hoffmann.