ORAL TOLERANCE INDUCED TO HOUSE-DUST MITE EXTRACT IN NAIVE AND SENSITIZED MICE - EVALUATION OF IMMUNOGLOBULIN-G ANTIIMMUNOGLOBULIN-E AUTOANTIBODIES AND IGG-IGE COMPLEXES
Mn. Sato et al., ORAL TOLERANCE INDUCED TO HOUSE-DUST MITE EXTRACT IN NAIVE AND SENSITIZED MICE - EVALUATION OF IMMUNOGLOBULIN-G ANTIIMMUNOGLOBULIN-E AUTOANTIBODIES AND IGG-IGE COMPLEXES, Immunology, 95(2), 1998, pp. 193-199
We investigated the effect on specific antibody response of naive and
sensitized mice orally administrated with low (0.25 mg) or high (10.0
mg) doses of Dermatophagoides pteronyssinus (Dp) extract. We also exam
ined the effect of oral administration of Dp on the production of auto
antibodies to immunoglobulin G (IgC) and immunoglobulin E (IEE). Naive
and sensitized mice both showed a marked down-regulation of IEE antib
ody production, regardless of the dose of DF We also detected an inhib
itory effect of the total ISE levels and the allergen-specific IgG1, I
gG2a and IgG2b antibody response in sensitized mice given the low dose
of Dp. In contrast, high doses of Dp stimulated IgG1 antibody product
ion in both naive and sensitized animals. In addition, the oral tolera
nce induction protocol stimulated anti-F(ab')(2 gamma) and anti-Fc gam
ma autoantibody production. Evaluation of Ige anti-IgE autoantibodies
by a direct enzyme immunoassay (EIA) revealed the presence of these au
toantibodies, predominantly of the IgG1 isotype, specifically in those
animals fed with the high dose. In contrast, IgG-IgE complexes, deter
mined by EIA using immobilized anti-IgE antibodies, were detected main
ly in sera of control animals. The autoantibody anti-IgE specificity w
as tested against IgE-TNP and IgE-DANSYL murine proteins and revealed
different inhibition profiles, suggesting the action of heterogeneous
subpopulations of autoantibodies. Taken together, our results show tha
t the oral tolerance protocol with Dp was able to modulate the product
ion of allergen-specific IgE antibodies in both naive and sensitized a
nimals. In addition, we suggest that anti-IgE autoantibodies participa
te in the modulation of allergic response triggered by oral tolerance
protocols.