PERITONEAL-MACROPHAGES FROM C57BL 6 MICE ORALLY IMMUNIZED WITH TOXOPLASMA-GONDII ANTIGENS IN ASSOCIATION WITH CHOLERA-TOXIN POSSESS AN ENHANCED ABILITY TO INHIBIT PARASITE MULTIPLICATION/
I. Bourguin et al., PERITONEAL-MACROPHAGES FROM C57BL 6 MICE ORALLY IMMUNIZED WITH TOXOPLASMA-GONDII ANTIGENS IN ASSOCIATION WITH CHOLERA-TOXIN POSSESS AN ENHANCED ABILITY TO INHIBIT PARASITE MULTIPLICATION/, FEMS immunology and medical microbiology, 12(2), 1995, pp. 121-126
Gamma-interferon (IFN-gamma) has been reported robe a major mediator o
f resistance to toxoplasma infection, mainly through macrophage activa
tion. Cholera toxin used as oral adjuvant induces enhanced protection.
Following oral immunization of C57BL/6 mice with a Toxoplasma gondii
sonicate (TSo), in association with either cholera toxin (CT) or its B
subunit (CTB), the ability of primed sensitized peritoneal macrophage
s (PM phi) to prevent T. gondii intracellular proliferation in vitro w
as examined both with and without rIFN-gamma activation. Under these c
onditions, the inhibition of T. gondii multiplication was greatly enha
nced in PM phi from mice immunized with a TSo and CT as an oral adjuva
nt. In contrast, PM phi from mice immunized with a TSo in association
with CTB showed a decrease in their microbiostatic activity towards T.
gondii. This negative effect on IFN-gamma-treated PM phi was cancelle
d out by the addition of a small amount of CT in association with TSo
and CTB in the immunization regimen. These data suggest that CT could
act as an oral adjuvant in vaccination against toxoplasmosis by increa
sing the microbiostatic activity of M phi activated with IFN-gamma. Fu
rther studies, using intestinal effector cells such as enterocytes, ar
e needed to confirm the value of CT for enhancing this major mechanism
of protection against T. gondii infection.