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:
2025,
Volume and Issue:
26(5), P. 1898 - 1898
Published: Feb. 22, 2025
Virus-induced
antibodies
represent
a
dual-edged
sword
in
the
immune
response
to
viral
infections.
While
are
critical
for
neutralizing
pathogens,
some
can
paradoxically
exacerbate
disease
severity
through
mechanisms
such
as
antibody-dependent
enhancement
(ADE),
autoantibody,
and
prolonged
inflammation.
Long
coronavirus
(COVID)
dengue
hemorrhagic
fever
(DHF)
exemplify
conditions
where
pathogenic
play
pivotal
role
progression.
COVID
is
associated
with
persistent
dysregulation
autoantibody
production,
leading
chronic
symptoms
tissue
damage.
In
DHF,
pre-existing
against
virus
contribute
ADE,
amplifying
replication,
activation,
vascular
permeability.
This
review
explores
underlying
these
antibody
responses,
highlighting
shared
pathways
of
comparing
distinct
features
both
conditions.
By
examining
studies,
we
identify
key
lessons
therapeutic
strategies,
vaccine
design,
future
research
aimed
at
mitigating
severe
outcomes
Wiener klinische Wochenschrift,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 22, 2025
Summary
Objective
Following
recovery
from
COVID-19,
there
is
evidence
for
pulmonary
sequelae
and
functional
impairment.
Data
regarding
the
immunopathological
mechanisms
are
limited.
This
study
aimed
to
investigate
relationship
between
bronchoalveolar
lavage
fluid
(BALF)
cellularity,
lung
function
impairment
high-resolution
computed
tomography
(HRCT)
changes
in
post-COVID
syndrome
patients.
Methods
Patients
with
were
enrolled
this
Austrian
single-center
prospective
observational
cohort
study.
All
patients
underwent
a
test
(PFT)
chest
HRCT.
Those
pathological
HRCT
findings
bronchoscopy
BALF
sampling
differential
cell
count
fluorescence-activated
sorting
analysis.
Results
In
26
BAL.
The
showed
ground-glass
opacifications
(69.2%),
organizing
pneumonia
(7.7%)
or
both
(11.5%).
PFT
revealed
restrictive
disease
38.5%
reduced
diffusion
capacity
68%,
19.2%
BAL
pattern
predominantly
consisting
of
CD4
+
T‑cells.
lymphocyte
was
associated
forced
vital
(
p
=
0.016)
an
elevated
alveolar-arterial
oxygen
gradient
0.04).
Conclusion
A
notable
percentage
persistent
T‑helper
lymphocytic
inflammation
lungs.
degree
alveolar
lymphocytosis
could
suggest
that
prolonged
inflammatory
response
compartment
contributes
pathogenesis
syndrome.
Clinical Immunology,
Journal Year:
2025,
Volume and Issue:
277, P. 110502 - 110502
Published: April 25, 2025
Following
SARS-CoV-2
infection,
some
individuals
develop
Long-COVID-syndrome
lasting
for
more
than
3
months.
We
analyzed
blood
samples
from
patients
with
Long-COVID,
controls
without
persistent
symptoms
following
SARS-CoV-2-infection
and
non-infected
donors
a
history
of
infection.
Long-COVID
showed
clear
signs
T
cell
hyper-activation
predominantly
in
the
CD8+
subset
4-fold
higher
expression
CD25
2-fold
effector-memory
cells.
polyclonal
stimulation,
we
found
stronger
upregulation
7-fold
release
IL-3
Long-COVID.
Intracellular
staining
revealed
5-fold
IL-3-expressing
cells
while
GM-CSF,
IFN-γ
IL-2
were
much
less
upregulated.
These
changes
correlated
severity
persisted
up
to
18
months
after
Our
data
reveal
pronounced
long-lasting
hyper-reactivity
speak
trial
cell-immunosuppression
Viruses,
Journal Year:
2025,
Volume and Issue:
17(5), P. 619 - 619
Published: April 25, 2025
SARS-CoV-2
infection
has
had
a
significant
impact
on
global
health
through
both
acute
illness,
referred
to
as
coronavirus
disease
2019
(COVID-19),
and
chronic
conditions
(long
COVID
or
post-acute
sequelae
of
COVID-19,
PASC).
Despite
substantial
advancements
in
preventing
severe
COVID-19
cases
vaccination,
the
rise
prevalence
long
syndrome
notable
degree
genomic
mutation,
primarily
S
protein,
underscores
necessity
for
deeper
understanding
underlying
pathophysiological
mechanisms
related
protein
SARS-CoV-2.
In
this
review,
latest
part
series,
we
investigate
potential
molecular
triggered
by
interaction
between
spike
cellular
receptors.
Therefore,
review
aims
provide
differential
focused
view
potentially
activated
binding
canonical
non-canonical
receptors
SARS-CoV-2,
together
with
their
possible
interactions
effects
pathogenesis
COVID.
PLoS ONE,
Journal Year:
2025,
Volume and Issue:
20(4), P. e0321811 - e0321811
Published: April 29, 2025
Background
It
is
estimated
that
at
least
10%
of
the
population
infected
with
SARS-CoV-2
develop
Post
COVID
Condition,
which
characterized
by
a
diverse
array
symptoms
including
dyspnea,
fatigue,
anxiety,
depression,
and
deterioration
in
quality
life.
The
virus
can
trigger
an
excessive
immune
response,
release
pro-inflammatory
cytokines
IL-6,
IL-1,
TNFα
reactive
oxygen
species.
Specialized
Pro
Resolving
Mediators
(SPMs)
(17-HAD,
14-HAD
18_HEPE)
could
be
useful
Condition
modulating
inflammatory
response.
objective
to
determine
change
life,
profile,
functional
capacity
emotional
variables
group
taking
nutritional
supplement
plus
telerehabilitation
programme.
Methods
ARACOV-2
study
double-blind,
parallel-group,
randomized
control
trial
two
parallel
interventions:
Nutritional
vs
placebo
telerehabilitation.
primary
endpoint
will
life
(EQ-5L-5D).
intervention
last
12
weeks
daily
intake
omega-3
or
supervised
rehabilitation
programme
using
Discussion
This
suggests
SPMs
supplementation
combined
may
improve
inflammation
like
fatigue
patients.
Both
interventions
have
anti-inflammatory
potential,
their
use
enhance
physical
mental
health
outcomes.
approach
offers
promising
strategy
for
managing
symptoms.
Trial
registration
ClinicalTrials.gov
NCT06063031
International Journal of Infectious Diseases,
Journal Year:
2024,
Volume and Issue:
142, P. 106966 - 106966
Published: Feb. 15, 2024
Various
mechanisms,
such
as
immune
dysregulation,
viral
reservoir,
and
auto-immunity,
are
hypothesized
to
underlie
the
pathogenesis
of
long-term
health
problems
after
hospitalization
for
COVID-19.
We
aimed
assess
effect
in-hospital
COVID-19
treatments
on
prominent
problems.
Journal of Translational Medicine,
Journal Year:
2024,
Volume and Issue:
22(1)
Published: March 26, 2024
Abstract
Background
Post
COVID-19
condition
(PCC)
is
a
complication
of
SARS-COV-2
infection
and
can
lead
to
long-term
disability.
Methods
The
present
study
was
designed
analyse
the
gene
expression
patterns
PCC
through
bulk
RNA
sequencing
whole
blood
explore
potential
molecular
mechanisms
PCC.
Whole
collected
from
80
participants
enrolled
in
prospective
cohort
following
SARS-CoV-2
infected
non-infected
individuals
for
6
months
after
recruitment
used
sequencing.
Identification
differentially
expressed
genes
(DEG),
pathway
enrichment
immune
cell
deconvolution
performed
biological
pathways
involved
Results
We
have
found
13
associated
with
Enriched
were
related
interferon-signalling
anti-viral
processes.
Conclusion
transcriptome
characterized
by
modest
overexpression
interferon-stimulated
genes,
pointing
subtle
ongoing
inflammatory
response.
Reproductive Biology and Endocrinology,
Journal Year:
2024,
Volume and Issue:
22(1)
Published: June 7, 2024
Abstract
Fatigue,
an
increasingly
acknowledged
symptom
in
various
chronic
diseases,
has
garnered
heightened
attention,
during
the
medical
era
of
bio-psycho-social
model.
Its
persistence
not
only
significantly
compromises
individual’s
quality
life
but
also
correlates
with
organ
damage.
Surprisingly,
intricate
relationship
between
fatigue
and
female
reproductive
health,
specifically
infertility,
remains
largely
unexplored.
Our
exploration
into
existing
body
evidence
establishes
a
compelling
link
uterine
ovarian
as
well
conditions
associated
such
rheumatism.
This
observation
suggests
potentially
pivotal
role
influencing
overall
fertility.
Furthermore,
we
propose
hypothetical
mechanism
elucidating
impact
on
infertility
from
multiple
perspectives,
postulating
that
neuroendocrine,
neurotransmitter,
inflammatory
immune,
mitochondrial
dysfunction
resulting
its
co-factors
may
further
contribute
to
endocrine
disorders,
menstrual
irregularities,
sexual
dysfunction,
ultimately
leading
infertility.
In
addition
providing
this
comprehensive
theoretical
framework,
summarize
anti-fatigue
strategies
accentuate
current
knowledge
gaps.
By
doing
so,
our
aim
is
offer
novel
insights,
stimulate
research,
advance
understanding
crucial
interplay
health.
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(15), P. 8056 - 8056
Published: July 24, 2024
This
study
explores
the
role
of
inflammation
and
oxidative
stress,
hallmarks
COVID-19,
in
accelerating
cellular
biological
aging.
We
investigated
early
molecular
markers—DNA
methylation
age
(DNAmAge)
telomere
length
(TL)—in
blood
leukocytes,
nasal
cells
(NCs),
induced
sputum
(IS)
one
year
post-infection
pauci-
asymptomatic
healthcare
workers
(HCWs)
infected
during
first
pandemic
wave
(February–May
2020),
compared
to
COPD
patients,
model
for
“aged
lung”.
Data
from
questionnaires,
Work
Ability
Index
(WAI),
analyses,
autonomic
cardiac
balance
assessments,
heart
rate
variability
(HRV),
pulmonary
function
tests
were
collected.
Elevated
leukocyte
DNAmAge
significantly
correlated
with
advancing
age,
male
sex,
daytime
work,
an
aged
phenotype
characterized
by
chronic
diseases,
elevated
LDL
glycemia
levels,
medications
affecting
HRV,
declines
lung
function,
WAI,
lymphocyte
count,
hemoglobin
HRV
(p
<
0.05).
Increasing
job
positions
involving
intensive
patient
contact,
higher
counts
collectively
contributed
shortened
TL
Notably,
HCWs
exhibited
accelerated
aging
IS
both
leukocytes
≤
0.05)
NCs
0.001)
biologically
older
than
patients
These
findings
suggest
need
monitor
COVID-19
survivors,
who
represent
majority
general
population.