In this article is a summary of our recent findings on the role of nitric o
xide (NO) as an effector mechanism against the intracellular parasite, Leis
hmania major. NO is produced in large amounts in murine macrophages followi
ng activation by IFN gamma synthesized by Th1 cells. NO production is inhib
ited by IL-4, a product of Th2 cells. A set of stable cell surface markers
has now been identified. ST2L and IL-18R are selectively expressed on Th2 a
nd Th1 cells respectively. Antibody against ST2L can down-regulate Th2 cell
s in the highly susceptible BALB/c mice leading to control of otherwise fat
al L. major infection. These results show directly the critical role of the
balance between Th1 and Th2 cells in cutaneous leishmaniasis. (C) 1999 Els
evier Science B.V. All rights reserved.