International Journal of Molecular Sciences,
Journal Year:
2023,
Volume and Issue:
24(8), P. 7053 - 7053
Published: April 11, 2023
Lipidomics
is
a
term
used
to
define
the
field
that
analyzes
structure,
functions,
and
interactions
of
lipids.
Inflammatory
dermatoses
lipid
disturbances
are
interrelated,
especially
due
chronic
inflammatory
conditions.
This
review
discusses
lipidomics
in
selected
skin
diseases:
psoriasis,
lichen
planus,
atopic
dermatitis,
as
well
less
commonly
mentioned
hidradenitis
suppurativa,
rosacea,
acne
vulgaris.
Lipid
homeostasis
disorders
common;
they
well-documented
dermatitis.
Future
studies
required
for
better
insight
into
this
issue,
particularly
on
lipidome.
Understanding
lipidomics,
particular
diseases,
increases
our
knowledge
about
their
pathogenesis,
may
become
useful
adjusting
tailored
management
each
patient
establishing
prognosis.
Noteworthily,
it
seems
advisable
alert
doctors
need
analyze
parameters
complications
abnormal
metabolism
dermatological
patients,
which
could
decrease
comorbidities
improve
life
quality
health
condition
patients.
New England Journal of Medicine,
Journal Year:
2021,
Volume and Issue:
384(12), P. 1136 - 1143
Published: March 24, 2021
Atopic
dermatitis
is
a
chronic
disorder
that
usually
starts
in
childhood
but
often
persists
adulthood.
The
appearance
and
extent
of
lesions
vary
with
age
race
or
ethnic
group.
Topical
systemic
treatments
targeting
the
underlying
immune
condition
have
been
introduced.
Annals of Allergy Asthma & Immunology,
Journal Year:
2021,
Volume and Issue:
126(4), P. 417 - 428.e2
Published: Jan. 9, 2021
Little
is
known
on
the
current
global
prevalence
of
atopic
dermatitis
(AD)
in
pediatric
population.To
estimate
real-world
AD
population
and
by
disease
severity.This
international,
cross-sectional,
web-based
survey
children
adolescents
(6
months
to
<18
years
old)
was
conducted
following
18
countries:
North
America
(Canada,
United
States),
Latin
(Argentina,
Brazil,
Columbia,
Mexico),
Europe
(France,
Germany,
Italy,
Spain,
Kingdom),
Middle
East
Eurasia
(Israel,
Saudi
Arabia,
Turkey,
Arab
Emirates,
Russia),
Asia
(Japan,
Taiwan).
Prevalence
determined
using
2
definitions:
(1)
diagnosed
as
having
according
International
Study
Asthma
Allergies
Childhood
(ISAAC)
criteria
self-
or
parent-report
ever
being
told
a
physician
that
they
their
child
had
(eczema);
(2)
reported
based
ISAAC
only.
Severity
assessed
Patient
Global
Assessment
(PtGA)
Patient-Oriented
Eczema
Measure
(POEM).Among
65,661
responders,
12-month
(ISAAC
plus
self-reported
diagnosis)
ranged
from
2.7%
20.1%
across
countries;
only)
13.5%
41.9%.
Severe
evaluated
with
both
PtGA
POEM
generally
less
than
15%;
more
subjects
rated
mild
suggested
POEM.
No
trends
were
observed
age
sex;
lower
rural
residential
settings
urban
suburban.This
countries
revealed
affects
substantial
proportion
population.
Although
severity
varied
groups
countries,
15%
severe
AD.
Journal of Clinical Investigation,
Journal Year:
2019,
Volume and Issue:
129(4), P. 1493 - 1503
Published: March 10, 2019
A
rapidly
developing
paradigm
for
modern
health
care
is
a
proactive
and
individualized
response
to
patients’
symptoms,
combining
precision
diagnosis
personalized
treatment.
Precision
medicine
becoming
an
overarching
medical
discipline
that
will
require
better
understanding
of
biomarkers,
phenotypes,
endotypes,
genotypes,
regiotypes,
theratypes
diseases.
The
100-year-old
allergen-specific
management
allergic
diseases
has
particularly
contributed
early
awareness
in
medicine.
Polyomics,
big
data,
systems
biology
have
demonstrated
profound
complexity
dynamic
variability
disease
between
individuals,
as
well
regions.
Escalating
costs
together
with
questionable
efficacy
the
current
facilitated
emergence
endotype-driven
approach.
We
describe
here
approach
stratifies
patients
based
on
mechanisms
optimize
JAMA Dermatology,
Journal Year:
2019,
Volume and Issue:
155(12), P. 1358 - 1358
Published: Oct. 9, 2019
Molecular
profiling
of
skin
biopsies
is
the
criterion
standard
for
evaluating
cutaneous
atopic
dermatitis
(AD)
phenotype.
However,
are
not
always
feasible
in
children.
A
reproducible
minimally
invasive
approach
that
can
track
disease
pediatric
longitudinal
studies
or
clinical
trials
lacking.To
assess
a
using
tape
strips
to
identify
biomarkers
may
serve
as
surrogate
identified
whole-tissue
biopsies.This
cross-sectional
study
51
children
younger
than
5
years
recruited
with
moderate
severe
AD
and
without
from
dermatology
outpatient
clinics
at
children's
hospital.
Sixteen
were
serially
collected
nonlesional
lesional
21
who
had
less
6
months
initiation
normal
30
did
have
between
January
22,
2016,
April
20,
2018.Gene
protein
expression
evaluated
quantitative
real-time
polymerase
chain
reaction
immunohistochemistry.A
total
included
study;
duration,
AD.
Of
AD,
mean
(SD)
age
was
1.7
(1.7)
years,
most
male
(15
[71.4%]
white
[71.4%]).
1.8
(2.0)
female
(20
[66.7%])
(22
[73.3%]).
Seventy-seven
79
immune
barrier
gene
products
detected
(gene
detection
rate,
97%)
70
71
(sample
99%),
53
markers
differentiating
and/or
Many
cellular
T
cells
(CD3),
AD-related
dendritic
(Fc
ε
RI
OX40
ligand
receptors),
key
inflammatory
(matrix
metallopeptidase
12),
innate
(interleukin
8
[IL-8]
IL-6),
helper
cell
2
(TH2;
IL-4,
IL-13,
chemokines
CCL17
CCL26),
TH17/TH22
(IL-19,
IL-36G,
S100A
proteins)
genes
significantly
increased
compared
skin.
For
example,
IL-4
(SE)
-15.2
(0.91)
-19.5
(0.48);
P
<
.001.
Parallel
decreases
occurred
epidermal
(FLG,
CLDN23,
FA2H)
negative
regulators
(IL-34
IL-37).
decrease
FLG
-2.9
(0.42)
2.2
(0.45);
Associations
found
severity
transepidermal
water
loss
TH2
(IL-33
IL-4R)
(IL-36G
S100As)
(evaluated
SCORing
Atopic
Dermatitis,
Eczema
Area
Severity
Index,
Pruritus
Dermatitis
Quickscore
tools).In
this
study,
provide
alternative
AD-associated
prove
useful
tracking
therapeutic
response
predicting
future
course
comorbidities.
Cellular and Molecular Immunology,
Journal Year:
2023,
Volume and Issue:
20(5), P. 448 - 474
Published: March 16, 2023
Atopic
dermatitis
(AD)
is
the
most
common
inflammatory
skin
disease,
and
it
considered
a
complex
heterogeneous
condition.
Different
phenotypes
of
AD,
defined
according
to
patient
age
at
onset,
race,
ethnic
background;
disease
duration;
other
characteristics,
have
been
recently
described,
underlying
need
for
personalized
treatment
approach.
Recent
advancements
in
understanding
AD
pathogenesis
resulted
real
translational
revolution
led
exponential
expansion
therapeutic
pipeline.
The
study
biomarkers
clinical
studies
emerging
treatments
helping
clarify
role
each
cytokine
immune
pathway
will
allow
addressing
unique
fingerprints
subset.
Personalized
medicine
be
ultimate
goal
this
targeted
research.
In
review,
we
discuss
changes
concepts
both
approach
highlight
scientific
rationale
behind
report
recent
efficacy
data.
British Journal of Dermatology,
Journal Year:
2023,
Volume and Issue:
189(5), P. 531 - 539
Published: July 18, 2023
Abstract
Background
Atopic
dermatitis
(AD)
is
an
inflammatory
skin
disease
with
significant
unmet
need.
Blockade
of
the
OX40–OX40
ligand
(OX40L)
costimulation
pathway
by
targeting
OX40L
on
antigen-presenting
cells
(APCs)
a
fully
human
noncytotoxic,
nondepleting
anti-OX40L
monoclonal
antibody
(amlitelimab;
SAR445229;
KY1005)
novel
way
to
modulate
persistent
inflammation.
Objectives
To
assess
safety
and
efficacy
amlitelimab
over
16
weeks
in
adults
AD
phase
IIa
double-blind
placebo-controlled
study.
Methods
The
study
was
conducted
at
19
hospitals
Germany,
Poland,
Spain
UK.
Eligible
patients
moderate-to-severe
were
randomized
(1
:
1
1)
low-dose
intravenous
(IV)
(200
mg),
high-dose
IV
(500
mg)
or
placebo,
followed
three
maintenance
doses
(50%
loading
dose)
4,
8
12
weeks,
follow-up
week
36.
co-primary
endpoints
incidence
treatment-emergent
adverse
events
(all
who
received
≥
dose
drug)
mean
percentage
change
Eczema
Area
Severity
Index
(EASI)
(full
analysis
set).
Results
Between
13
December
2018
May
2020,
89
randomly
assigned
low-
(n
=
29)
30)
placebo
29),
whom
88
proceeded
treatment
[37
women
(42%),
51
(58%)
men;
(SD)
age
33.6
(11.9)
years].
Amlitelimab
generally
well
tolerated
unremarkable
profile;
no
hypersensitivity
reported.
For
primary
endpoint,
least
square
EASI
from
baseline
–80.12%
[95%
confidence
interval
(CI)
–95.55
–64.68;
P
0.009
vs.
placebo]
–69.97%
(95%
CI
–85.04
–54.60;
0.07
placebo)
for
27)
groups,
respectively,
–49.37%
–66.02
–32.72)
24).
Numerically
greater
reductions
observed
2
16.
Conclusions
Novel
OX40L-expressing
APCs
resulted
clinically
meaningful
improvements
AD.