Recurrent vulvovaginal candidiasis (RVVC) is a common idiopathic mucosal in
fection caused by Candida albicans. Current data suggests that local immuni
ty is more important than that in the peripheral circulation for protection
against infection. In the present study, anti-Candida innate resistance at
the vaginal mucosa was investigated using a murine model. For this, spleni
c and vaginal cells were assessed for ir? vitro growth inhibition (GI) of C
. albicans and cytotoxicity of natural killer (NK) cell-sensitive tumour ta
rgets (YAC-1). As expected, significant GI of C. albicans by splenic cells
was mediated predominantly by polymorphonuclear leucocytes (PMNL) at effect
or to target (E:T) ratios of 100 and 50.1. From the vaginal mucosa, naive u
nfractionated, but not nylon wool non-adherent (NWN), cells extracted from
whole vaginal tissue showed significant GI of C. albicans at E:T ratios as
low as 1:1, but only modest killing of YAC-1 targets at all E:T ratios. Sub
sequent experiments showed significant GI of C, albicans by vaginal epithel
ioid-enriched cells and with several epithelial cell lines, but not in supe
rnatants collected from the co-cultures. In contrast, lymphoid cell lines h
ad no anti-Candida activity. These results suggest that anti-Candida activi
ty is present at the vaginal mucosa, but unlike that from the spleen, the v
aginal activity appears to be predominantly mediated by epithelial cells.