ORAL-ADMINISTRATION OF ONE DOSE OF CHOLERA-TOXIN INDUCES A SYSTEMIC IMMUNE-RESPONSE PRIOR TO A MUCOSAL IMMUNE-RESPONSE BY A DIRECT PRESENTATION IN THE SPLEEN
R. Benedetti et al., ORAL-ADMINISTRATION OF ONE DOSE OF CHOLERA-TOXIN INDUCES A SYSTEMIC IMMUNE-RESPONSE PRIOR TO A MUCOSAL IMMUNE-RESPONSE BY A DIRECT PRESENTATION IN THE SPLEEN, Immunology letters, 60(2-3), 1998, pp. 149-156
In the present report the results indicate that the oral administratio
n of one dose of CT in rats results in an antibody immune response in
the spleen 48 h later, whereas no antitoxin antibody forming cells wer
e found in the Peyer patches (PP), mesenteric lymph node (MLN) and lam
ina propria (LP) of the small intestine. At this time the main isotype
of the antitoxin antibodies in the spleen were IgG and IgM, 5 days af
ter the priming, few antitoxin AFC were observed in the MLN, IgG being
the main isotype, whereas no IgM antitoxin AFC were found. At 1 week
after priming the number of antitoxin AFC in the MLN reached similar v
alues to those observed in the spleen. When cells from the spleen of r
ats primed orally with one dose of CT were cultured during 4 days in t
he presence of inhibitory doses of anti-Ia MAb (OX6), the number of an
titoxin AFC was diminished when compared with that observed when cells
were cultured in the absence of anti-Ia. The main isotype of antitoxi
n AFC observed when cells were analyzed after culture was IgM and it w
as the isotype most affected by the treatment with MAb anti-Ia. These
results strongly suggest that an in situ presentation of the antigen d
id occur in the spleen. On the other hand, when the secondary immune r
esponse was studied 48 h after boosting, antitoxin AFC were found in t
he PP, MLN, SP and LP and 5 days after the booster a 20-30-fold increa
se was observed in all lymphoid tissues studied, indicating that the s
econdary immune response found in the spleen was mainly due to the rec
ruitment of memory cells from Peyer's patches. However, when spleen ce
lls were cultured 48 h after the immunization in the presence of inhib
itory doses of anti-Ia a little decrease in the number of AFC was obse
rved when compared with the controls (in absence of anti-Ia). The anal
ysis of the antitoxin antibodies in sera and intestinal fluids were in
line with the results presented above. The results shown in this repo
rt indicate that the systemic immune response observed after the oral
administration of CT could be due in part to an in situ presentation o
f the antigen in the systemic compartments, especially in the spleen.
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