Background:
Recent
epidemiological
studies have
indicated that early
life receipt of
antibiotics may be
associated with an
increased risk of
developing atopic
disorder. Lysed
Enterococcus
faecalis FK-23 (LFK),
a probiotic product
of E faecalis, has
been shown to have
inhibitory effects
on allergen-induced
immune responses in
mice.
Objective:
The purpose of this
study was to
evaluate the effects
of LFK on immune
responses and
intestinal
microflora in
antibiotic-treated,
and allergen-sensitized
weaning mice.
Methods:
Three-week-old BALB/c
mice were sensitized
with cedar pollen
allergen to
establish the
experimental model.
The allergen induced
peritoneal
accumulation of
eosinophils, serum
levels of total and
allergen-specific
immunoglobulin (Ig)
E and IgG2a, and the
intestinal bacterial
fl ora were
determined in the
control, antibiotic,
LFK and antibiotic-LFK
groups (n = 7 in all
groups). Orally
administered
erythromycin, one
kind of macrolide
antibiotic, was used
for the experiments.
Results:
There was no signifi
cant difference in
the allergen-induced
peritoneal
accumulation of
eosinophils and
serum specifi c IgE
and IgG2a levels in
erythromycin-treated
mice compared to a
control group.
However, the ratio
of serum total IgE
to IgG2a levels was
signifi cantly
increased in
erythromycin-treated
mice relative to
that found either in
LFK-treated mice or
in erythromycin-treated
mice with LFK
supplementation. The
total aerobes, total
anaerobes and
Enterococcus species
of intestinal
microflora were not
signifi cantly
different among all
groups.
Lactobacillus
species were
distinctly
eliminated in the
mice exposed to
erythromycin on day
7 and totally
recovered in
erythromycin-treated
mice with LFK
intervention on day
28, but could not be
recovered in the
erythromycin-treated
mice without LFK
intervention.
Conclusions:
Our results suggest
that LFK may improve
the intestinal
ecosystem disturbed
by antibiotic use,
and thereby prevent
subsequent
development of atopy.
However, whether
different
antibiotics have
different effects on
immune responses
needs to be
addressed further.
Key words:
Antibiotics.
Eosinophils.
Immunoglobulins.
Intestinal
microflora.
Enterococcus
faecalis.
Lactobacillus.
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