“…Therefore, a partially protective vaccine would be effective (Bergquist, 2002;Pearce, 2003). Studies on the use of Sm14 for the development of an antihelminth vaccine seem set to continue at a steady pace, as this antigen has shown a consistent ability to induce partially protective immunity in animal models, both mice (for S. mansoni) and sheep (final host for F. hepatica), when delivered by a variety of recombinant vectors being investigated for vaccine development (Nascimento et al, 2002;Vilar et al, 2003;Abreu et al, 2004;Fonseca et al, 2004;Varaldo et al, 2004). Only the rBCG system, however, was shown to induce significant protection using a single dose immunization regime (Varaldo et al, 2004).…”