One of the most characteristic clinical features in cutaneous leishmaniasis
is the development of nodules followed by ulcerations at the site of infec
tion. Leishmania amazonensis-infected mice show similar ulcerative lesions.
Leishmania-infected severe combined immunodeficiency (SCID) mice, however,
have been shown to develop nonulcerative nodules. In the present study, th
e roles of T cells in ulceration were examined using SCID mice in cell reco
nstitution experiments. After development of nonulcerative nodules, SCID mi
ce were inoculated with splenocytes from either Leishmania-infected or naiv
e immunocompetent mice, resulting in ulceration in all mice. When naive spl
enocytes were depleted of CD4(+), CD8(+), or B220(+) cell populations and t
he remaining cells were injected into Leishmania-infected SCID mice after t
he development of nodules, only SCID mice inoculated with splenocytes deple
ted of CD4(+) cells did not show ulceration. The evidence obtained in this
study clearly shows that the CD4(+) cell population is indispensable for ul
ceration in leishmaniasis lesions of SCID mice.