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IL-17A regulates Eimeria tenella schizont maturation and migration in avian coccidiosis.
[wiskott-aldrich syndrome]
Although
IL
17
A
is
associated
with
the
immunological
control
of
various
infectious
diseases
,
its
role
in
host
response
to
Eimeria
infections
is
not
well
understood
.
In
an
effort
to
better
dissect
the
role
of
IL
17
A
in
host-pathogen
interactions
in
avian
coccidiosis
,
a
neutralizing
antibody
(
Ab
)
to
chicken
IL
17
A
was
used
to
counteract
IL
17
A
bioactivity
in
vivo
.
Chickens
infected
with
Eimeria
tenella
and
treated
intravenously
with
IL
17
A
Ab
,
exhibited
reduced
intracellular
schizont
and
merozoite
development
,
diminished
lesion
score
,
compared
with
untreated
controls
.
Immunohistological
evaluation
of
cecal
lesions
in
the
parasitized
tissues
indicated
reduced
migration
and
maturation
of
second
-generation
schizonts
and
reduced
lesions
in
lamina
propria
and
submucosa
.
In
contrast
,
untreated
and
infected
chickens
had
epithelial
cells
harboring
second
-generation
schizonts
,
which
extend
into
the
submucosa
through
muscularis
mucosa
disruptions
,
maturing
into
second
generation
merozoites
.
Furthermore
,
IL
17
A
Ab
treatment
was
associated
with
increased
parameters
of
Th
1
immunity
(
IL
2
-
and
IFN
γ-
producing
cells
)
,
reduced
levels
of
reactive
oxygen
species
(
ROS
)
,
and
diminished
levels
of
serum
matrix
metalloproteinase-
9
(
MMP-
9
)
.
Finally
,
schizonts
from
untreated
and
infected
chickens
expressed
S
100
,
Wiskott-
Aldrich
syndrome
protein
family
member
3
(
WASF
3
)
,
and
heat
shock
protein-
70
(
HSP
70
)
proteins
as
merozoites
matured
,
whereas
the
expression
of
these
proteins
was
absent
in
IL
17
A
Ab
-treated
chickens
.
These
results
provide
the
first
evidence
that
the
administration
of
an
IL
17
A
neutralizing
Ab
to
E
.
tenella-infected
chickens
inhibits
the
migration
of
parasitized
epithelial
cells
,
markedly
reduces
the
production
of
ROS
and
MMP-
9
,
and
decreases
cecal
lesions
,
suggesting
that
IL
17
A
might
be
a
potential
therapeutic
target
for
coccidiosis
control
.
Diseases
Validation
Diseases presenting
"increased parameters of th1 immunity"
symptom
wiskott-aldrich syndrome
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