Abstract
In
this
study,
we
use
integrated
transcriptomic
datasets
from
the
GEO
repository
with
purpose
of
investigating
immune
dysregulation
in
COVID-19.
Thus,
context,
decided
to
be
focused
on
NK
cells
and
CD14+
monocytes
gene
expression,
considering
GSE165461
GSE198256,
respectively.
Other
PBMCs,
lung,
olfactory,
sensory
epithelium
lymph
were
used
provide
robust
validation
for
our
results.
This
approach
gave
an
view
responses
COVID-19,
pointing
out
a
set
potential
biomarkers
therapeutic
targets
special
regard
standards
physiological
conditions.
IFI27,
MKI67,
CENPF,
MBP,
HBA2,
TMEM158,
THBD,
HBA1,
LHFPL2,
SLA,
AC104564.3
identified
as
key
genes
analysis
that
have
critical
biological
processes
related
inflammation,
regulation,
oxidative
stress,
metabolic
processes.
Consequently,
such
are
important
understanding
heterogeneous
clinical
manifestations
COVID-19—from
acute
long-term
effects
now
known
‘long
COVID’.
Subsequent
additional
consolidated
these
role
diagnosis
COVID-19
prediction
its
severity.
Moreover,
their
enrichment
pathophysiological
pathways
presented
them
intervention.The
results
insight
into
molecular
dynamics
caused
by
other
monocytes.
study
constitutes
solid
basis
targeted
diagnostic
development
makes
relevant
contributions
ongoing
research
efforts
toward
better
management
mitigation
pandemic.
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(12), P. 6389 - 6389
Published: June 9, 2024
Long
COVID
(LC),
also
referred
to
as
Post
COVID-19
Condition,
Post-Acute
Sequelae
of
SARS-CoV-2
Infection
(PASC),
and
other
terms,
represents
a
complex
multisystem
disease
persisting
after
the
acute
phase
COVID-19.
Characterized
by
myriad
symptoms
across
different
organ
systems,
LC
presents
significant
diagnostic
management
challenges.
Central
disorder
is
role
low-grade
inflammation,
non-classical
inflammatory
response
that
contributes
chronicity
diversity
observed.
This
review
explores
pathophysiological
underpinnings
LC,
emphasizing
importance
inflammation
core
component.
By
delineating
pathogenetic
relationships
clinical
manifestations
this
article
highlights
necessity
for
an
integrated
approach
employs
both
personalized
medicine
standardized
protocols
aimed
at
mitigating
long-term
consequences.
The
insights
gained
not
only
enhance
our
understanding
but
inform
development
therapeutic
strategies
could
be
applicable
chronic
conditions
with
similar
features.
Immunologic Research,
Journal Year:
2024,
Volume and Issue:
72(4), P. 654 - 664
Published: Feb. 20, 2024
Abstract
Moyamoya
disease
(MMD)
is
a
cerebrovascular
disorder
marked
by
progressive
arterial
narrowing,
categorized
into
six
stages
known
as
Suzuki
based
on
angiographic
features.
Growing
evidence
indicates
pivotal
role
of
systemic
immune
and
inflammatory
responses
in
the
initiation
advancement
MMD.
This
study
employs
high-dimensional
mass
cytometry
to
reveal
immunophenotypic
characteristics
peripheral
blood
cells
(PBMCs)
at
various
stages,
offering
insights
progression
PBMC
samples
from
eight
patients
with
early-stage
MMD
(Suzuki
II
III)
later-stage
IV,
V,
VI)
were
analyzed
using
evaluate
frequency
phenotype
cell
subtypes.
We
identified
15
clusters
found
that
immunological
features
are
composed
cluster
variations.
In
this
study,
we
confirmed
that,
compared
MMD,
group
exhibits
an
increase
non-classical
monocytes.
As
stage
level
increases,
proportions
plasmacytoid
DCs
monocyte-derived
decrease.
Furthermore,
T
cells,
monocytes,
DCs,
PMN-MDSCs
show
activation
canonical
NF-κB
signaling
pathway.
summarized
similarities
differences
between
patients.
There
potential
circulating
dysfunction
onset
development
Brain Behavior & Immunity - Health,
Journal Year:
2025,
Volume and Issue:
43, P. 100934 - 100934
Published: Jan. 5, 2025
A
considerable
proportion
(21%)
of
patients
with
common
variable
immunodeficiency
(CVID)
suffers
from
depression.
These
subjects
are
characterized
by
reduced
naïve
T
cells
and
a
premature
cell
senescence
similar
to
that
major
depressive
disorder
(MDD).
It
is
known
essential
for
limbic
system
development/function.
Treatment
thymosin
α1
(Tα1)
capable
increase
the
thymus
output
cells.
To
treat
CVID
comorbid
episode
Tα1
thereby
improve
mood.
small
open-label,
proof
concept
trial.
Five
depressed
(Hamilton
Depression
Rating
Scale,
HDRS
>12)
could
be
treated
(8
weeks,
1.6
mg
daily
subcutaneously,
1st
week,
thereafter
twice
weekly).
At
start,
at
8
weeks
after
last
injection,
was
recorded
blood
samples
drawn
measuring
memory
cells,
Th17
Treg
hsCRP,
IL-6
IL-7.
Outcomes
were
compared
those
contrast
group
(42
MDD
patients,
same
severity
but
as
usual
(TAU)).
In
all
5
decreased
during
treatment
(with
average
52%,
TAU
scores
36%
in
patients).
All
showed
an
naïve/memory
CD4+
CD8+
ratios,
4
detectable
levels
reductions
recorded.
did
not
show
such
immune
improvements.
8-week
wash-out,
depression
recurred
2
most
severe
while
continued
others.
Immune
effects
sustained
wash-out.
This
preliminary
study
suggests
hormone
have
antidepressive
related
correcting
effects.
Data
urge
larger
placebo-controlled
trials.
Biomedicines,
Journal Year:
2025,
Volume and Issue:
13(2), P. 428 - 428
Published: Feb. 10, 2025
The
Severe
Acute
Respiratory
Syndrome
Coronavirus
2
(SARS-CoV-2)
pandemic
has
imposed
several
medical
and
economic
challenges
since
its
onset
in
2019.
This
is
due
to
ability
target
the
respiratory
system
as
well
other
organs,
resulting
significant
impacts
necessitating
organ
transplants.
Our
goal
compile
information
from
existing
literature
investigate
how
COVID-19
affects
outcomes
following
transplantation.
A
comprehensive
search
was
conducted
studies
reporting
post-COVID-19
complications.
We
included
45
data
related
solid
transplants,
where
either
recipient,
organ,
or
donor
affected
by
SARS-CoV-2.
majority
of
concluded
that
transplantation
infection
could
be
performed
safely
with
similar
non-COVID-19
patients,
regardless
whether
donor,
recipient
COVID-19.
No
deviation
standard
immunosuppression
regimens
surgical
protocols
necessary
either,
further
re-assuring
feasibility
these
transplants
viable
treatment
options.
applies
involving
lungs,
kidneys,
liver,
heart.
However,
there
a
limited
number
some
areas,
which
warrants
need
for
additional
research
order
reach
more
concrete
conclusions
pertaining
COVID-19’s
effect
on
HIV Infection and Immunosuppressive Disorders,
Journal Year:
2025,
Volume and Issue:
16(4), P. 7 - 16
Published: Feb. 12, 2025
Aim
of
the
study:
to
investigate
role
proinflammatory
markers
and
some
immune
cells
in
neural
cognitive
disorders
long
COVID
patients.
Materials
methods.
The
study
included
81
patients
diagnosed
with
COVID,
presence
which
was
determined
by
persistence
a
complex
multidirectional
symptoms
for
more
than
12
weeks
that
developed
during
or
after
COVID-19.
Flow
cytometry
used
assess
lymphocyte
subsets.
main
subpopulations
were
analyzed:
T
cells,
cytotoxic
B
NK
NKT
blood
plasma
via
multiplex
xMAP
analysis.
Also
concentrations
GM-CSF,
IL-1,
IL-2,
IL-4,
IL-5,
IL-6,
IL-8,
IL-12,
IL-13,
IL-17,
MCP-1,
MIP-1b,
TNF
measured.
content
cytokines
system
characterized
respondents
COVID.
A
comparative
analysis
data
conducted
individuals
without
history
COVID-19,
as
well
between
different
numbers
SARS-CoV-2
cases.
Results
discussion.
identified
characteristic
features
affect
both
nervous
systems.
Analysis
revealed
absolute
relative
lymphopenia
due
decrease
cells.
We
also
noticed
an
increased
number
who
suffered
multiple
when
compared
those
only
infected
once.
Cytokine
increase
IL-17
CCL2/MCP1
Conclusion.
provides
additional
support
theory
dysregulation
neurological
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 19, 2025
Abstract
Long-term
adverse
consequences
of
SARS-CoV-2
infection,
termed
“long
COVID”
or
post-acute
sequelae
COVID
(PASC),
are
a
major
component
overall
COVID-19
disease
burden.
Prior
obesity
and
metabolic
increase
the
severity
acute
disease,
but
infection
also
contributes
to
development
new-onset
disease.
Since
pandemic
occurred
in
context
global
epidemic,
an
important
question
is
extent
which
pre-existing
modifies
long-term
responses
infection.
We
utilized
nonhuman
primate
model
compare
effects
with
delta
variant
lean
obese/insulin-resistant
adult
male
rhesus
macaques
over
6-month
time
course.
While
some
longitudinal
including
viral
dynamics,
SARS-CoV-2-specific
IgG
induction,
cytokine
profiles,
tissue
persistence
RNA,
did
not
appreciably
differ
between
obese
animals,
other
responses,
neutralizing
Ab
lung
pathology,
body
weight,
degree
insulin
sensitivity,
adipocytokine
temperature,
nighttime
activity
levels
were
significantly
different
versus
animals.
Furthermore,
several
parameters
animals
altered
following
resemble
those
Notably,
persistent
changes
multiple
present
most
suggesting
that
PASC
may
be
more
prevalent
than
estimated
from
self-reported
symptoms
human
studies.