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Neutrophil extracellular traps regulate IL-1β-mediated inflammation in familial Mediterranean fever.
[familial mediterranean fever]
Inflammatory
attacks
of
familial
Mediterranean
fever
(
FMF
)
are
characterised
by
circulation
and
influx
of
high
number
of
polymorphonuclear
neutrophils
(
PMN
)
in
the
affected
sites
and
profound
therapeutic
effect
of
IL
-
1
β
inhibitors
.
We
investigated
the
role
of
neutrophil
extracellular
traps
(
NET
)
in
the
pathogenesis
of
FMF
,
and
their
involvement
in
IL
-
1
β
production
.
Blood
samples
were
obtained
from
six
FMF
patients
during
remissions
and
from
three
patients
during
attacks
.
NET
formation
and
NET
components
were
studied
by
fluorescence
techniques
,
immunobloting
and
MPO
-DNA
complex
ELISA
.
PMNs
from
patients
released
NETs
decorated
with
IL
-
1
β
during
disease
attacks
.
On
the
other
hand
,
PMNs
from
patients
during
remission
were
resistant
to
inflammatory
stimuli
that
induce
NET
release
in
PMNs
from
control
subjects
.
Lower
basal
autophagy
levels
were
identified
in
PMNs
during
remission
,
while
induction
of
autophagy
facilitated
NET
release
,
suggesting
that
autophagy
is
involved
in
the
regulation
of
NET
release
.
During
the
resolution
of
attacks
,
inhibition
of
NET
formation
by
negative
feedback
mechanism
was
also
observed
.
The
anti-
inflammatory
agents
,
colchicine
and
DNAse
I
,
inhibited
IL
-
1
β
production
in
PMNs
and
IL
-
1
β
activity
in
NETs
,
respectively
.
We
suggest
two
additive
events
for
triggering
the
FMF
attack
;
the
production
of
IL
-
1
β
by
PMNs
and
its
release
through
NETs
.
At
the
same
time
NETs
,
homeostatically
,
downregulate
further
NETosis
,
facilitating
the
resolution
of
attack
.
Compensatorly
,
lower
basal
autophagy
of
PMNs
may
protect
from
crises
by
attenuating
the
release
of
pro-
inflammatory
NETs
.
Diseases
Validation
Diseases presenting
"fever"
symptom
22q11.2 deletion syndrome
acute rheumatic fever
alexander disease
allergic bronchopulmonary aspergillosis
canavan disease
carcinoma of the gallbladder
child syndrome
congenital toxoplasmosis
cushing syndrome
cystinuria
dracunculiasis
erdheim-chester disease
esophageal adenocarcinoma
esophageal carcinoma
familial mediterranean fever
focal myositis
hodgkin lymphoma, classical
lamellar ichthyosis
legionellosis
locked-in syndrome
malignant atrophic papulosis
neonatal adrenoleukodystrophy
neuralgic amyotrophy
oculocutaneous albinism
papillon-lefèvre syndrome
pyomyositis
pyruvate dehydrogenase deficiency
scrub typhus
severe combined immunodeficiency
sneddon syndrome
systemic capillary leak syndrome
triple a syndrome
typhoid
waldenström macroglobulinemia
wolf-hirschhorn syndrome
This symptom has already been validated