Leishmaniases are caused by protozoan parasites of the genus Leishmania. Th
eir clinical features may vary from self-limiting cutaneous lesions to syst
emic and fatal forms. Various vaccines have been evaluated in mice and/or h
umans against cutaneous leishmaniasis mainly. Some vaccines use non pathoge
n mutants, others killed parasites the immunogenicity of which is enhanced
by the co-injection of immune microorganisms of the Bacille Calmette-Guerin
type. However the in vivo protection of such vaccines is inconstant, altho
ugh skin-test reactivity, T-cell proliferation, or interferon-gamma product
ion in response to leishmanial antigens is elevated when compared to placeb
o. Some antigenic proteins (i.e. gp63 or lipophosphoglycan), whether purifi
ed or expressed by recombinant microorganisms, seem to be of interest Recom
binant viruses or bacteria, expressing leishmanial antigens, have been succ
essfully used too. (C) 2000 Editions scientifiques et medicales Elsevier SA
S.