Life,
Journal Year:
2023,
Volume and Issue:
13(2), P. 419 - 419
Published: Feb. 2, 2023
Interleukin
17
(IL-17)
is
an
effector
cytokine
that
plays
a
key
role
in
the
pathogenesis
of
both
psoriasis
and
metabolic-associated
fatty
liver
disease
(MAFLD),
condition
more
prevalent
severe
patients
with
psoriasis.
In
inflammation,
IL-17
mainly
produced
by
CD4+
T
(TH17)
CD8+
cells
(Tc17),
although
numerous
other
(macrophages,
natural
killer
cells,
neutrophils
Tγδ
cells)
also
contribute
to
production
IL-17.
hepatocytes,
mediates
systemic
inflammation
recruitment
inflammatory
liver,
it
implicated
development
fibrosis
insulin
resistance.
levels
have
been
correlated
progression
from
MAFLD
steatohepatitis,
cirrhosis,
even
hepatocellular
carcinoma.
Clinical
trials
shown
inhibiting
IL-17A
could
potentially
improvement
metabolic
parameters.
A
better
understanding
factors
involved
these
chronic
processes
lead
efficient
treatment
for
MAFLD,
help
develop
holistic
strategies
improve
management
patients.
International Journal of Molecular Sciences,
Journal Year:
2019,
Volume and Issue:
20(18), P. 4347 - 4347
Published: Sept. 5, 2019
Psoriasis
is
an
immune-mediated
genetic
skin
disease.
The
underlying
pathomechanisms
involve
complex
interaction
between
the
innate
and
adaptive
immune
system.
T
cells
interact
with
dendritic
cells,
macrophages,
keratinocytes,
which
can
be
mediated
by
their
secreted
cytokines.
In
past
decade,
biologics
targeting
tumor
necrosis
factor-α,
interleukin
(IL)-23,
IL-17
have
been
developed
approved
for
treatment
of
psoriasis.
These
dramatically
changed
management
contrast,
various
triggering
factors
elicit
disease
in
genetically
predisposed
individuals.
Recent
studies
suggest
that
exacerbation
psoriasis
lead
to
systemic
inflammation
cardiovascular
comorbidity.
addition,
may
associated
other
auto-inflammatory
auto-immune
diseases.
this
review,
we
summarize
risk
factors,
divided
into
two
groups
(namely,
extrinsic
intrinsic
factors),
responsible
onset
order
facilitate
its
prevention.
Gut Microbes,
Journal Year:
2022,
Volume and Issue:
14(1)
Published: July 22, 2022
The
human
intestine
hosts
diverse
microbial
communities
that
play
a
significant
role
in
maintaining
gut-skin
homeostasis.
When
the
relationship
between
gut
microbiome
and
immune
system
is
impaired,
subsequent
effects
can
be
triggered
on
skin,
potentially
promoting
development
of
skin
diseases.
mechanisms
through
which
affects
health
are
still
unclear.
Enhancing
our
understanding
connection
needed
to
find
novel
ways
treat
disorders.
In
this
review,
we
systematically
evaluate
current
data
regarding
ecology
healthy
gut,
diet,
pre-
probiotics,
antibiotics,
their
health.
We
discuss
potential
axis
link
skin-associated
diseases,
such
as
psoriasis,
atopic
dermatitis,
acne
vulgaris,
rosacea,
alopecia
areata,
hidradenitis
suppurativa.
This
review
will
increase
impacts
conditions
aid
finding
new
medications
for
Microbiome,
Journal Year:
2021,
Volume and Issue:
9(1)
Published: May 30, 2021
Abstract
The
skin
is
the
exterior
interface
of
human
body
with
environment.
Despite
its
harsh
physical
landscape,
colonized
by
diverse
commensal
microbes.
In
this
review,
we
discuss
recent
insights
into
microbial
populations,
including
their
composition
and
role
in
health
disease
modulation
intrinsic
extrinsic
factors,
a
focus
on
pathobiological
basis
aging.
We
also
describe
most
tools
for
investigating
microbiota
microbe-skin
relationships
perspectives
regarding
challenges
microbiome
manipulation.
International Journal of Molecular Sciences,
Journal Year:
2021,
Volume and Issue:
22(8), P. 3998 - 3998
Published: April 13, 2021
Numerous
scientific
studies
in
recent
years
have
shown
significant
skin
and
gut
dysbiosis
among
patients
with
psoriasis.
A
decrease
microbiome
alpha-diversity
(abundance
of
different
bacterial
taxa
measured
one
sample)
as
well
beta-diversity
(microbial
diversity
samples)
was
noted
psoriasis
skin.
It
has
been
proven
that
the
representation
Cutibacterium,
Burkholderia
spp.,
Lactobacilli
is
decreased
Corynebacterium
kroppenstedii,
simulans,
Neisseria
Finegoldia
spp.
increased
comparison
to
healthy
Alterations
are
similar
those
observed
inflammatory
bowel
disease.
In
two
diseases,
F.
prausnitzii,
Bifidobacterium
Lactobacillus
Parabacteroides
Coprobacillus
were
underrepresented,
while
abundance
Salmonella
sp.,
Campylobacter
Helicobacter
Escherichia
coli,
Alcaligenes
Mycobacterium
sp.
increased.
Several
research
provided
evidence
for
influence
treatments
on
a
positive
orally
administered
probiotics
course
this
dermatosis.
Further
needed
determine
development
diseases.
The
changes
under
treatment
can
serve
potential
biomarker
response
therapy.
Frontiers in Cellular and Infection Microbiology,
Journal Year:
2022,
Volume and Issue:
12
Published: March 7, 2022
The
human
skin
harbors
a
wide
variety
of
microbes
that,
together
with
their
genetic
information
and
host
interactions,
form
the
microbiome.
role
microbiome
in
development
various
diseases
has
lately
gained
interest.
According
to
several
studies,
changes
cutaneous
microbiota
are
involved
pathophysiology
dermatoses.
A
better
delineation
its
interactions
innate
adaptive
immune
systems
could
lead
understanding
these
diseases,
as
well
opportunity
achieve
new
therapeutic
modalities.
present
review
centers
on
most
recent
knowledge
participation
pathogenesis
disorders:
atopic
seborrheic
dermatitis,
alopecia
areata,
psoriasis
acne.
Biomedicines,
Journal Year:
2022,
Volume and Issue:
10(5), P. 1037 - 1037
Published: April 30, 2022
Evidence
has
shown
that
gut
microbiome
plays
a
role
in
modulating
the
development
of
diseases
beyond
gastrointestinal
tract,
including
skin
disorders
such
as
psoriasis.
The
gut-skin
axis
refers
to
bidirectional
relationship
between
and
health.
This
is
regulated
through
several
mechanisms
inflammatory
mediators
immune
system.
Dysregulation
microbiota
been
seen
numerous
conditions
atopic
dermatitis,
rosacea,
Understanding
how
are
involved
regulating
health
may
lead
novel
therapies
for
these
modulation,
particularly
In
this
review,
we
will
compare
psoriasis
patients
healthy
control,
explain
concept
effects
dysbiosis
on
physiology.
We
also
review
current
evidence
using
probiotics
Cell Communication and Signaling,
Journal Year:
2024,
Volume and Issue:
22(1)
Published: Feb. 12, 2024
Abstract
Psoriasis
is
an
immune-mediated
inflammatory
skin
disease,
involving
a
complex
interplay
between
genetic
and
environmental
factors.
Previous
studies
have
demonstrated
that
factors
play
major
role
in
the
pathogenesis
of
psoriasis.
However,
non-genetic
are
also
necessary
to
trigger
onset
recurrence
psoriasis
genetically
predisposed
individuals,
which
include
infections,
microbiota
dysbiosis
gut,
dysregulated
lipid
metabolism,
sex
hormones,
mental
illness.
can
be
induced
by
other
triggers,
such
as
trauma,
unhealthy
lifestyles,
medications.
Understanding
how
these
triggers
provides
insights
into
pathogenesis,
well
better
clinical
administration.
In
this
review,
we
summarize
for
update
current
evidence
on
underlying
mechanism
elicit
disease.
Frontiers in Immunology,
Journal Year:
2021,
Volume and Issue:
12
Published: July 23, 2021
Psoriasis
is
an
immune-mediated
systemic
disease
with
associated
comorbidities,
including
metabolic
syndrome
(MetS)
which
contributes
substantially
to
premature
mortality
in
patients
psoriasis.
However,
the
pathological
mechanisms
underlying
this
comorbidity
are
unclear.
Studies
have
shown
that
parameters
of
psoriasis
mediate
development
MetS.
We
reviewed
potential
association
between
and
MetS,
endoplasmic
reticulum
stress,
pro-inflammatory
cytokine
releases,
excess
production
reactive
oxygen
species,
alterations
adipocytokine
levels
gut
microbiota
dysbiosis.
Here,
we
highlight
important
research
questions
regarding
offer
insights
into
MetS
treatment.
International Journal of Molecular Sciences,
Journal Year:
2021,
Volume and Issue:
22(9), P. 4529 - 4529
Published: April 26, 2021
Psoriasis
is
a
chronic,
immune-mediated
inflammatory
disease
that
affects
around
125
million
people
worldwide.
Several
studies
concerning
the
gut
microbiota
composition
and
its
role
in
pathogenesis
recently
demonstrated
significant
alterations
among
psoriatic
patients.
Certain
parameters
such
as
Firmicutes/Bacteroidetes
ratio
or
Microbiome
Index
were
developed
order
to
distinguish
between
healthy
individuals.
The
“leaky
syndrome”
bacterial
translocation
considered
by
some
authors
triggering
factor
for
onset
of
disease,
it
promotes
chronic
systemic
inflammation.
also
found
resemble
those
bowel
diseases,
obesity
certain
cardiovascular
diseases.
Microbiota
dysbiosis,
depletion
SCFAs
production,
increased
amount
produced
TMAO,
dysregulation
pathways
affecting
balance
lymphocytes
populations
seem
be
most
findings
physiology
may
serve
potential
response-to-treatment
biomarker
cases
biological
treatment.
Oral
probiotics
administration
well
fecal
microbial
transplantation
reported
bringing
health
benefits
However,
issue
composition,
healing
needs
further
investigation.
Here
we
reviewed
literature
on
current
state
relationship
psoriasis
microbiome.
Scientific Reports,
Journal Year:
2020,
Volume and Issue:
10(1)
Published: July 29, 2020
Abstract
Psoriasis
is
an
immune-mediated
skin
disorder.
Imbalance
of
gut
microbial
populations
has
been
implicated
in
many
diseases.
We
aimed
to
investigate
whether
there
were
differences
microbiota
psoriasis
patients
vs
non-psoriasis
controls
and
between
severity
groups.
55
27
included.
V3–V4
regions
the
16S
rRNA
gene
fecal
samples
analyzed
using
Illumina
MiSeq.
Bioinformatic
analysis
was
performed.
found
changes
microbiome
composition
depending
on
their
status
as
determined
by
weighted
unifrac
(p
<
0.05),
particular
increase
Firmicutes
depletion
Bacteroidetes
patients.
Additionally,
Faecalibacterium
Blautia
genus
higher
while
Bacteroides
Paraprevotella
0.05,
LDA
score
>
2).
Moderate-to-severe
had
lower
biodiversity
than
mild
psoriatic
=
0.049).
No
for
beta-diversity
found.
developed
a
Psoriasis-Microbiota
Index
(PMI),
which
discriminated
among
with
sensitivity:
0.78
specificity:
0.79.
Furthermore,
we
performed
meta-analysis
published
data
validate
this
index.
demonstrated
dysbiosis
patients,
suggesting
role
pathophysiology.
PMI
potential
discriminate
across
different
populations,
could
be
used
biomarker
clinical
practice.