Recent progress in the treatment of visceral leishmaniasis includes pa
rticulate formulations of amphotericin B, which are highly effective,
and immunotherapy with interferon-gamma. Cutaneous leishmaniasis respo
nds better to intravenous pentamidine than previously realized, and to
pical treatment with paromycin may be effective in the Americas as wel
l as in the Middle East. The immunological basis for susceptibility an
d resistance to leishmaniasis is still being characterized in the muri
ne model, providing insight into human disease and the development of
immunogenic peptides with adjuvant cytokines for vaccines.