Persistent and recurrent infection of mucosal surfaces with Candida albican
s is common, ranging from a nuisance to a life threatening clinical problem
. No effective prophylactic or therapeutic vaccine has been developed. We h
ave studied a mouse model of oral candida infection to identify regulatory
and effector molecules of T cell activation as parameters of induced immuni
ty, and here describe the use of this model to determine an optimal immunis
ation strategy. Oral immunisation with the blastospore yeast form (but not
subcutaneous immunisation) induced clinical immunity, with a shift in param
eters of cytokine response characterised by an early and sustained producti
on of both IFN-gamma and IL-4 from antigen-stimulated cervical node T lymph
ocytes. (C) 2001 Elsevier Science Ltd. All rights reserved.