Prophylactic DNA vaccination protects mice against infection with Leishmani
a major by inducing an exclusive Th1 immune response dominated by the produ
ction of IFN-gamma. Here we show that DNA vaccines, initially designed to p
revent infection, can also have a significant therapeutic effect. In L. maj
or infected mice, vaccination with DNA encoding the Parasite Surface Antige
n/gp46/M2 causes reduction in lesion size and promotes healing in both gene
tically resistant C3H/He mice and susceptible BALB/c mice. The therapeutic
effect is underpinned by a shift in the T cell-derived cytokine environment
with an increase in the IFN-gamma producing Th1 type cells. Application of
such immunotherapy in conjunction with antiparasite drugs may result in fa
ster or more certain cure of the disease in humans. (C) 2000 Elsevier Scien
ce Ltd. All rights reserved.