Psikhiatriya,
Journal Year:
2025,
Volume and Issue:
22(5), P. 49 - 58
Published: Jan. 8, 2025
Background:
the
damaging
effect
of
ethanol
on
cells,
systems
and
organs
determines
relevance
studying
role
immune
system
in
pathogenesis
alcohol
dependence
(alcoholism).
The
literature
reported
contradictory
data
effects
cellular
immunity
that
is
conditioned
by
various
research
techniques,
approaches
to
formation
groups,
disease
stages.
Objective:
determine
phenotypes
lymphocytes
peripheral
blood
from
patients
with
time
course
post
withdrawal
state.
Patients:
52
male
aged
30–60
years
were
examinedwho
diagnosed
according
ICD-10
Mental
Behavioral
Disorders
due
Use
Alcohol
(dependence
syndrome
—
F10.21
F10.30),
their
duration
was
15.0
±
9.5
years,
including
12
alcoholic
liver
(ALD).
investigations
conducted
post-withdrawal
state:
after
detoxification
(1
point)
days
14–17
treatment
(2
point).
25
conditionally
healthy
men
served
as
controls,
comparison
group
included
20
neurotic
disorders.
Methods:
populations/subpopulations
determined
cytometer
BD
FACS
Calibur
(Becton
Dickinson,
USA);
reagent
kits
same
firm
used.
T-lymphocytes
(CD3+
),
B-lymphocytes
(CD19+
T-helpers/Т-inducers
CD4+
cytotoxic
Т-lymphocytes
CD8+
NK
cells
(CD3–CD16+
CD56+
)
revealed
percent
population
absolute
values.
Results:
point
1
study,
patients,
relation
controls
group,
had
an
elevated
Т-helpers-inducers,
a
reduced
number
cells.
After
therapy,
CD3+
remain
elevated,
decrease;
(ALD)
reduced.
Conclusion:
phenotype
alcohol-dependent
at
early
stage
postwithdrawal
state
characterized
elevation
,
reduction
During
some
populations
are
normalized,
except
for
T-lymphocytes,
well
ALD.
Immune
imbalance
indicates
instability
need
additional
treatment.
Diseases,
Journal Year:
2024,
Volume and Issue:
12(4), P. 69 - 69
Published: March 29, 2024
Alcoholic
liver
disease
(ALD)
is
a
major
cause
of
chronic
disease.
This
term
covers
broad
spectrum
lesions,
from
simple
steatosis
to
alcoholic
hepatitis
and
cirrhosis.
The
pathogenesis
ALD
multifactorial
not
fully
elucidated
due
complex
mechanisms
related
direct
ethanol
toxicity
with
subsequent
hepatic
systemic
inflammation.
accumulation
pro-inflammatory
cytokines
the
reduction
anti-inflammatory
promote
development
progression
ALD.
To
date,
there
are
no
targeted
therapies
counter
alcohol-related
prevent
acute
failure.
Corticosteroids
reduce
mortality
by
acting
on
hepatic-systemic
On
other
hand,
several
studies
analyzed
effect
inhibiting
stimulating
as
potential
therapeutic
targets
in
narrative
review
aims
clarify
role
main
involved
treatment
AJP Cell Physiology,
Journal Year:
2024,
Volume and Issue:
326(5), P. C1556 - C1562
Published: April 15, 2024
Healthy
livers
contain
80%
of
body
resident
macrophages
known
as
Kupffer
cells.
In
diseased
livers,
the
number
cells
usually
drops
but
is
compensated
by
infiltration
monocyte-derived
macrophages,
some
which
can
differentiate
into
Kupffer-like
Early
studies
suggest
that
play
important
roles
in
both
promoting
liver
injury
and
regeneration.
Yet,
distinction
between
functionalities
infiltrating
not
always
made.
By
using
more
specific
macrophage
markers
targeted
cell
depletion
single-cell
RNA
sequencing,
recent
revealed
several
subsets
functions
inducing
damage
inflammation
well
repair
this
review,
we
discuss
different
hepatic
necrotic
lesion
resolution
dead
clearance,
targeting
these
potential
tools
for
development
novel
therapies
acute
failure
acute-on-chronic
failure.
Frontiers in Cell and Developmental Biology,
Journal Year:
2025,
Volume and Issue:
12
Published: Jan. 7, 2025
Grafts
with
alcohol-associated
liver
disease
(ALD)
subjected
to
prolonged
cold
ischaemia
from
donors
after
brain
death
(DBD)
are
typically
unsuitable
for
transplantation.
Here,
we
investigated
the
role
of
growth
hormone
(GH)
in
livers
ALD
DBDs
and
its
relationship
vascular
endothelial
factor
A
(VEGFA)
VEGFB.
Livers
rats
fed
ethanol
6
weeks
(BD)
were
stored
24
h
ex
vivo
reperfusion.
Hepatic
damage
proliferative
inflammatory
parameters
analysed
BD,
before
graft
retrieval,
Survival
was
monitored
using
an
transplantation
model.
In
DBDs,
administration
GH,
which
increased
levels
intestine
but
not
liver,
induced
generation
both
VEGFA
VEGFB
protected
against
hepatic
caused
by
BD
retrieving
grafts
donors.
However,
only
that
ischemia
reperfusion,
also
survival
recipients.
conclusion,
signalling
pathway
beneficial
properties
GH-VEGFA/VEGFB
pathway,
intestine-liver
axis
plays
a
key
role,
disrupted
when
retrieved
Psikhiatriya,
Journal Year:
2025,
Volume and Issue:
22(5), P. 49 - 58
Published: Jan. 8, 2025
Background:
the
damaging
effect
of
ethanol
on
cells,
systems
and
organs
determines
relevance
studying
role
immune
system
in
pathogenesis
alcohol
dependence
(alcoholism).
The
literature
reported
contradictory
data
effects
cellular
immunity
that
is
conditioned
by
various
research
techniques,
approaches
to
formation
groups,
disease
stages.
Objective:
determine
phenotypes
lymphocytes
peripheral
blood
from
patients
with
time
course
post
withdrawal
state.
Patients:
52
male
aged
30–60
years
were
examinedwho
diagnosed
according
ICD-10
Mental
Behavioral
Disorders
due
Use
Alcohol
(dependence
syndrome
—
F10.21
F10.30),
their
duration
was
15.0
±
9.5
years,
including
12
alcoholic
liver
(ALD).
investigations
conducted
post-withdrawal
state:
after
detoxification
(1
point)
days
14–17
treatment
(2
point).
25
conditionally
healthy
men
served
as
controls,
comparison
group
included
20
neurotic
disorders.
Methods:
populations/subpopulations
determined
cytometer
BD
FACS
Calibur
(Becton
Dickinson,
USA);
reagent
kits
same
firm
used.
T-lymphocytes
(CD3+
),
B-lymphocytes
(CD19+
T-helpers/Т-inducers
CD4+
cytotoxic
Т-lymphocytes
CD8+
NK
cells
(CD3–CD16+
CD56+
)
revealed
percent
population
absolute
values.
Results:
point
1
study,
patients,
relation
controls
group,
had
an
elevated
Т-helpers-inducers,
a
reduced
number
cells.
After
therapy,
CD3+
remain
elevated,
decrease;
(ALD)
reduced.
Conclusion:
phenotype
alcohol-dependent
at
early
stage
postwithdrawal
state
characterized
elevation
,
reduction
During
some
populations
are
normalized,
except
for
T-lymphocytes,
well
ALD.
Immune
imbalance
indicates
instability
need
additional
treatment.