Cells,
Год журнала:
2023,
Номер
12(5), С. 676 - 676
Опубликована: Фев. 21, 2023
Measure
of
drug-mediated
immune
reactions
that
are
dependent
on
the
patient's
genotype
determine
individual
medication
protocols.
Despite
extensive
clinical
trials
prior
to
license
a
specific
drug,
certain
patient-specific
cannot
be
reliably
predicted.
The
need
for
acknowledgement
actual
proteomic
state
selected
individuals
under
drug
administration
becomes
obvious.
well-established
association
between
HLA
molecules
and
drugs
or
their
metabolites
has
been
analyzed
in
recent
years,
yet
polymorphic
nature
makes
broad
prediction
unfeasible.
Dependent
genotype,
carbamazepine
(CBZ)
hypersensitivities
can
cause
diverse
disease
symptoms
as
maculopapular
exanthema,
reaction
with
eosinophilia
systemic
more
severe
diseases
Stevens-Johnson-Syndrome
toxic
epidermal
necrolysis.
Not
only
HLA-B*15:02
HLA-A*31:01
but
also
HLA-B*57:01
CBZ
could
demonstrated.
This
study
aimed
illuminate
mechanism
HLA-B*57:01-mediated
hypersensitivity
by
full
proteome
analysis.
main
metabolite
EPX
introduced
drastic
alterations
induction
inflammatory
processes
through
upstream
kinase
ERBB2
upregulation
NFκB
JAK/STAT
pathway
implying
pro-apoptotic,
pro-necrotic
shift
cellular
response.
Anti-inflammatory
pathways
associated
effector
proteins
were
downregulated.
disequilibrium
pro-
anti-inflammatory
clearly
explain
fatal
following
administration.
Journal of Dermatological Treatment,
Год журнала:
2025,
Номер
36(1)
Опубликована: Фев. 26, 2025
Purpose
The
Appraisal
of
Guidelines
for
Research
and
Evaluation
II
Instrument
(AGREE
II)
was
developed
to
enhance
the
methodological
rigor
clinical
practice
guidelines
(CPGs),
aiming
generate
trustworthy
recommendations
various
scenarios.
Despite
its
importance,
there
exists
a
gap
in
quality
CPGs
pertaining
Stevens–Johnson
Syndrome
Toxic
Epidermal
Necrolysis
(SJS-TEN).
aim
study
evaluate
SJS-TEN
shed
light
on
areas
enhancing
guidelines'
quality.
Frontiers in Immunology,
Год журнала:
2025,
Номер
16
Опубликована: Март 18, 2025
Stevens
-
Johnson
syndrome/toxic
epidermal
necrolysis
(SJS/TEN)
is
a
life-threatening
adverse
reaction
to
nivolumab.
This
study
investigated
the
clinical
features
of
nivolumab
induced
SJS/TEN
provide
evidence
for
diagnosis
and
treatment.
Relevant
articles
on
published
before
December
31,
2024
were
collected
by
searching
database,
then
extracting
data
summary
analysis.
Thirty-one
patients
enrolled
with
median
age
65
years
(range
43,
86).
appear
at
5.5
weeks
(range,
0.9
108).
Bullae/blisters
(64.5%),
erythema
(54.8%),
skin
rash
detachment
(29.0%)
pain
main
symptoms.
Skin
biopsy
showed
necrosis
(41.9%),
keratinocytic
(38.7%),
interface
dermatitis
inflammatory
cell
infiltration
(45.2%).
After
stopping
receiving
treatment,
74.2%
had
improvement
in
symptoms,
22.6%
died
TEN.
As
rare
immune-related
event
nivolumab,
should
be
closely
monitored
during
Nivolumab
has
long
incubation
period,
serious
symptoms
poor
prognosis.
International Journal of Community Medicine and Public Health,
Год журнала:
2025,
Номер
12(4), С. 1900 - 1903
Опубликована: Март 28, 2025
This
case
report
presents
a
48-year-old
woman
with
history
of
chronic
kidney
disease
who
experienced
toxic
epidermal
necrolysis
(TEN),
also
known
as
Lyell's
syndrome,
an
uncommon
and
severe
adverse
drug
reaction.
The
TEN
was
attributed
to
the
use
non-steroidal
anti-inflammatory
drugs
(NSAIDs).
Cutaneous
involvement
exceeded
80%
body
surface
area
(BSA),
encompassing
ocular,
oral,
nasal
mucosa,
well
trunk,
bilateral
limbs,
genitalia.
Treatment
commenced
aggressive
fluid
resuscitation,
administration
cyclosporine,
meticulous
dermal
care.
patient
ultimately
discharged
following
approximately
one
month
intensive
therapy.
Stevens-Johnson
syndrome
(SJS)
and
toxic
epidermal
necrolysis
(TEN)
are
life-threatening
spectrum
diseases
in
which
a
medication
triggers
mucocutaneous
reaction
associated
with
severe
necrosis
loss
of
integrity.
The
disease
has
high
mortality
rate
that
can
be
assessed
by
dermatology
scoring
scales
based
on
an
affected
total
body
surface
area
(TBSA).
Sloughing
<10%
TBSA
is
considered
SJS,
10%.
>30%
termed
TEN,
increased
25%
to
35%.
We
present
case
management
TEN
involved
critically
ill
African
American
woman.
Identification
the
offending
agent
was
difficult
due
complicated
exposure
throughout
her
multi-facility
care
management.
This
conveys
importance
close
monitoring
patient
during
clinical
course
involving
SJS-/TEN-inducing
drugs.
also
discuss
potential
risks
for
SJS/TEN
population
genetic
or
epigenetic
predispositions
skin
conditions.
report
contributes
increasing
color
representation
current
literature.
Additionally,
we
use
Chat
Generative
Pre-trained
Transformer
(ChatGPT,
OpenAI
LP,
Inc.,
San
Francisco,
CA,
USA)
list
its
benefits
errors.
Dermatology and Therapy,
Год журнала:
2023,
Номер
13(6), С. 1305 - 1327
Опубликована: Май 13, 2023
Stevens-Johnson
syndrome
(SJS)
and
toxic
epidermal
necrolysis
(TEN)
are
severe
cutaneous
adverse
reactions
with
high
morbidity
mortality
not
clearly
established
treatment
protocol.
This
meta-analysis
aimed
to
evaluate
the
efficacy
safety
of
three
biologic
TNF-α
inhibitors
(infliximab,
etanercept,
adalimumab)
in
SJS,
SJS-TEN
overlap,
TEN.Electronic
databases
were
searched
for
original
studies
containing
human
participants
diagnosed
SJS/TEN
treated
inhibitors.
Individual
patient
data
collected
summarized
provide
a
comprehensive
overview
on
therapeutic
different
TEN,
respectively.
Meta-analyses
aggregated
study
conducted
using
random-effects
model.Overall,
55
125
sets
individual
included.
Infliximab
was
used
treat
3
patients
overlap
28
actual
rate
33.3%
17%,
Etanercept
administered
17
9
64
reported
be
0%,
12.5%,
For
no
significant
difference
found
time
reepithelialization,
hospitalization
time,
comparing
etanercept
infliximab.
More
sequelae
receiving
infliximab
than
(39.3%
versus
6.4%).
Adalimumab
four
25%.
revealed
significantly
shortened
compared
non-etanercept
groups
[weighted
mean
differences
(WMD)
-5.30;
95%
confidence
interval
(CI)
-8.65
-1.96].
associated
survival
benefit
when
treatment,
however,
analysis
statistically
(odds
ratio
0.55;
CI
0.23-1.33).On
basis
current
findings,
is
currently
most
promising
therapy
SJS/TEN.
Further
evaluation
prospective
required
confirm
its
safety.
International Journal of Environmental Research and Public Health,
Год журнала:
2023,
Номер
20(3), С. 2217 - 2217
Опубликована: Янв. 26, 2023
Toxic
epidermal
necrolysis,
Leyll's
syndrome
(TEN),
is
a
rare
mucocutaneous
blistering
disease
burdened
with
high
mortality
rates.
The
diagnosis
of
TEN
based
on
clinical
symptoms
and
histopathological
findings.
In
approximately
90%
cases,
it
severe
adverse
reaction
to
drugs.
TEN,
not
only
the
skin
affected,
but
also
mucosa
organs'
epithelium.
There
are
no
unequivocal
recommendations
in
regard
systemic
topical
treatment
patients.
aim
this
paper
review
available
literature
propose
unified
protocols
be
discussed.
Early
management
multidisciplinary
necessary
improve
patients'
outcome.
Treatment
patients
suspicions
should
initiated
early
drug
withdrawal.
patients,
like
burns,
require
intensive
care
management.
Each
patient
provided
adequate
fluid
resuscitation,
respiratory
support,
nutritional
treatment,
pain
control,
infection
prophylaxis,
anticoagulant
therapy,
gastric
ulcer
prophylaxis.
key
local
use
nonadherent
dressings
that
do
damage
epidermis
during
change.
purification
blood
stream
from
causative
agent.
most
efficient
way
clarify
serum
combination
plasmapheresis
IVIG.
Immunomodulatory
therapy
can
reduce
five
times
comparison
immunosuppression
or
lack
full
protocol.
Clinical Cosmetic and Investigational Dermatology,
Год журнала:
2023,
Номер
Volume 16, С. 457 - 461
Опубликована: Фев. 1, 2023
Sintilimab
is
a
recombinant
fully
human
anti-programmed
cell
death
protein
1
(PD-1)
monoclonal
antibody
that
blocks
the
interaction
of
PD-1
with
its
ligand.
It
was
approved
to
use
in
patients
gastric
malignancy.
Toxic
epidermal
necrolysis
(TEN)
rare,
life-threatening
cutaneous
drug
reaction.
Here,
we
report
70-year-old
female
patient
malignancy
who
developed
severe
TEN
10
days
after
initiation
sintilimab.
The
did
not
respond
systemic
corticosteroids
and
intravenous
immunoglobulin
therapies
but
improved
subcutaneous
injection
adalimumab
(40
mg)
directed
against
antitumor
necrosis
factor-α.
Her
rashes
rapidly
resolved
within
24
hr.
By
seventh
day,
bullae
had
scabbed
most
skin
lesions
subsided.
showed
no
sign
organ
dysfunction.
This
first
reported
case
immune
checkpoint
inhibitor-induced
successfully
treated
adalimumab.