Future Virology,
Год журнала:
2024,
Номер
19(14-15), С. 525 - 538
Опубликована: Окт. 12, 2024
COVID-19
causes
cytokine
storm
which
results
in
altered
iron
homeostasis
within
the
system.
The
negative
consequences
of
this
include
poor
metabolism,
ROS-induced
oxidative
damage,
ferroptosis,
and
increased
severity
along
with
illnesses
like
anemia,
thalassemia,
diabetes,
cancer,
neurological
disorders,
long
COVID.
Therefore,
managing
overload
natural
or
synthetic
chelators
alternative
therapeutics
can
help
to
reduce
COVID-19.
This
review
analyzes
intricate
molecular
mechanism
dynamics
during
SARS-CoV-2
infection
disease
progression
patients
related
clinical
consequences.
Also,
explores
a
comprehensive
understanding
reciprocal
between
their
adverse
effects,
thereby
facilitating
development
potential
therapeutic
interventions.
Clinical and Translational Allergy,
Год журнала:
2025,
Номер
15(3)
Опубликована: Март 1, 2025
Abstract
Background
COVID‐19
exhibits
a
variety
of
symptoms
and
may
lead
to
multi‐organ
failure
death.
This
clinical
complexity
is
exacerbated
by
significant
immune
dysregulation
affecting
nearly
all
cells
the
innate
adaptive
system.
Granulocytes,
including
eosinophils,
are
affected
SARS‐CoV‐2.
Objectives
Eosinophil
responses
remain
poorly
understood
despite
early
recognition
eosinopenia
as
hallmark
feature
severity.
Results
The
heterogeneous
nature
eosinophil
categorizes
them
dual‐function
with
contradictory
effects.
activation
can
suppress
virus‐induced
inflammation
releasing
type
2
cytokines
like
IL‐13
granular
proteins
antiviral
action
such
eosinophil‐derived
neurotoxins
cationic
protein,
also
acting
antigen‐presenting
cells.
In
contrast,
accumulation
in
lungs
induce
tissue
damage
triggered
or
hormones
IFN‐γ
leptin.
Additionally,
they
affect
functions
interacting
T
through
direct
formation
membrane
complexes
soluble
mediator
action.
Individuals
allergic
disorders
who
have
elevated
levels
eosinophils
tissues
blood,
asthma,
do
not
appear
be
at
an
increased
risk
developing
severe
following
SARS‐CoV‐2
infection.
However,
vaccine
appears
associated
complications
eosinophilic
infiltrate‐induced
immunopathogenicity,
which
mitigated
corticosteroid,
anti‐histamines
anti‐IL‐5
therapy
avoided
modifying
adjuvants
excipients.
Conclusion
review
highlights
importance
contributes
better
understanding
their
role
during
natural
infection
vaccination.
Biomedicines,
Год журнала:
2024,
Номер
12(4), С. 913 - 913
Опубликована: Апрель 20, 2024
Background:
Post-acute
sequelae
of
SARS-CoV-2
infection
(PASC)
is
a
complicated
disease
that
affects
millions
people
all
over
the
world.
Previous
studies
have
shown
PASC
impacts
10%
infected
patients
which
50–70%
are
hospitalised.
It
has
also
been
10–12%
those
vaccinated
against
COVID-19
were
affected
by
and
its
complications.
The
severity
later
development
symptoms
positively
associated
with
early
intensity
infection.
Results:
generated
health
complications
caused
involve
vast
variety
organ
systems.
Patients
diagnosed
neuropsychiatric
neurological
symptoms.
cardiovascular
system
involved
several
diseases
such
as
myocarditis,
pericarditis,
coronary
artery
reported.
Chronic
hematological
problems
thrombotic
endothelialitis
hypercoagulability
described
conditions
could
increase
risk
clotting
disorders
coagulopathy
in
patients.
Chest
pain,
breathlessness,
cough
respiratory
long-COVID
causing
distress
syndrome.
observed
immune
notable,
involving
diseases.
renal
was
impacted,
resulted
raising
issues,
fibrosis,
sepsis.
Endocrine
gland
malfunction
can
lead
to
diabetes,
thyroiditis,
male
infertility.
Symptoms
diarrhea,
nausea,
loss
appetite,
taste
among
reported
observations
due
gastrointestinal
disorders.
Skin
abnormalities
might
be
an
indication
long-term
implications
persistent
cutaneous
complaints
linked
PASC.
Conclusions:
Long-COVID
multidimensional
syndrome
considerable
public
implications,
affecting
physiological
systems
demanding
thorough
medical
therapy,
more
study
address
underlying
causes
effects
needed.
Frontiers in Immunology,
Год журнала:
2025,
Номер
15
Опубликована: Янв. 8, 2025
Acute
COVID-19
infection
causes
significant
alterations
in
the
innate
and
adaptive
immune
systems.
While
most
individuals
recover
naturally,
some
develop
long
COVID
(LC)
syndrome,
marked
by
persistent
or
new
symptoms
weeks
to
months
after
SARS-CoV-2
infection.
Despite
its
prevalence,
there
are
no
clinical
tests
distinguish
LC
patients
from
those
fully
recovered.
Understanding
immunological
basis
of
is
essential
for
improving
diagnostic
treatment
approaches.
We
performed
deep
immunophenotyping
functional
assays
examine
profiles
patients,
with
active
COVID-19,
recovered
healthy
donors.
This
analysis
assessed
both
features,
identifying
potential
biomarkers
syndrome.
A
Binomial
Generalized
Linear
Model
(BGLM)
was
used
pinpoint
features
characterizing
LC.
exhibited
depletion
cell
subsets,
including
plasmacytoid
conventional
dendritic
cells,
classical,
non-classical,
intermediate
monocytes,
monocyte-derived
inflammatory
cells.
Elevated
basal
inflammation
observed
compared
whose
were
closer
donors
individuals.
However,
displayed
alterations,
reduced
T
subsets
(CD4,
CD8,
Tregs)
switched
memory
B
similar
patients.
Through
BGLM,
a
unique
signature
identified,
featuring
CD8
gd
cells
low
proliferative
capacity
diminished
expression
activation
homing
receptors.
The
findings
highlight
associated
characterized
dysregulation.
recovery
comparable
Recovered
individuals,
deficits
populations
evident,
differentiating
full
recovery.
These
provide
insights
into
pathogenesis
may
support
development
tools
targeted
therapies.
Polskie Archiwum Medycyny Wewnętrznej,
Год журнала:
2023,
Номер
unknown
Опубликована: Ноя. 8, 2023
REVIEW
ARTICLE
D
-Dimers
and
venous
thromboembolism
1
extent
of
fibrinolysis,
clearance
fibrin
degradation
products.D
-Dimer
level
increases
physiologically
with
age
during
pregnancy
puerperium;
it
may
be
higher
in
African
-Americans
smokers.Increased
-dimer
is
also
observed
several
pathologic
conditions,
which
stabilized
formed
subsequently
degraded,
such
as
arterial
thrombosis,
infectious
diseases,
neoplasms,
trauma,
surgery,
liver
disease,
renal
insufficiency,
fibrinolytic
therapy,
disseminated
intravascular
coagulation
(DIC),
acute
coronary
syndromes,
cerebrovascular
events,
subarachnoid
hemorrhage,
obstetric
complications,
or
autoimmune
disorders.
3D
measurement
was
proposed
a
laboratory
test
for
the
diagnosis
DIC
1970s;
since
then
considerable
advances
have
been
made
regarding
its
measurement,
main
clinical
role
that
(VTE)
diagnosis.
2Introduction
During
hemostasis,
activation
leads
to
production
thrombin,
cleaves
fibrinogen
into
monomers
finally
form
polymer.Thrombin
activates
factor
XIII,
stabilizes
polymers
cross
-linked
covalent
bonds.Activation
fibrinolysis
plasmin,
various
fragments,
including
-dimers
(FIguRE
1).Plasmin
produces
different
products
molecular
weight
(MW)
ranging
from
190
over
10
000
kDa,
MW
about
180
kDa.
are
mainly
cleared
by
kidney
reticulo
-endothelial
system,
plasma
half
-life
6
8
hours.
1,2In
physiological
approximately
2%-3%
converted
fibrin,
degraded
system.
1,2As
result,
can
detected
low
amounts
healthy
individuals
under
conditions.Plasma
concentration
depends
on
XIIIa
-stabilized
formation,
Clinical and Experimental Medicine,
Год журнала:
2024,
Номер
24(1)
Опубликована: Янв. 17, 2024
Abstract
Long
Covid-19
syndrome
(LCS)
manifests
with
a
wide
range
of
clinical
symptoms,
yet
the
factors
associated
LCS
remain
poorly
understood.
The
current
study
aimed
to
investigate
relationships
that
demographic
characteristics,
history,
laboratory
indicators,
and
frequency
HLA-I
alleles
have
likelihood
developing
LCS.
We
extracted
characteristics
histories
from
medical
records
88
cases
(LCS
+
group)
96
individuals
without
−
group).
Furthermore,
we
evaluated
serum
levels
interleukin
(IL)-6
tumor
necrosis
factor-α,
parameters,
frequencies
alleles.
Following
this
used
multiple
logistic
regression
association
these
variables
had
Subjects
in
group
were
more
likely
experienced
severe
symptoms
higher
body
mass
index
(BMI),
white
blood
cell,
lymphocyte
counts,
C-reactive
protein
(CRP),
IL-6
than
those
(for
all:
P
<
0.05).
Moreover,
HLA-A*11,
-B*14,
-B*38,
-B*50,
-C*07
After
adjusting
for
most
important
variables,
suffering
was
significantly
BMI,
CRP,
IL-6,
alleles,
as
well
positive
history
Our
showed
during
acute
phase
disease,
elevated
CRP
levels,
all
an
increased
Life,
Год журнала:
2024,
Номер
14(4), С. 460 - 460
Опубликована: Апрель 1, 2024
In
severe
cases,
SARS-CoV-2
infection
leads
to
respiratory
failure.
Although
angiotensin-converting
enzyme
2
(ACE2)
receptors
are
not
expressed
in
red
blood
cells,
can
interact
with
cells
(RBCs)
via
several
or
auxiliary
membrane
proteins.
Recent
data
show
that
viral
causes
significant
damage
the
RBCs,
altering
their
morphology,
deformability,
and
aggregability.
Loss
of
RBC
deformability
and/or
increased
aggregability
favors
development
thrombotic
processes
microcirculation,
as
has
been
described
occur
COVID-19
patients.
addition,
many
patients
also
develop
systemic
endotheliitis
associated
generalized
coagulopathy.
This
manifests
itself
clinically
obstructive
microthrombi
area
medium
smallest
vessels,
which
affect
all
internal
organs.
It
is
thought
such
changes
RBCs
may
contribute
microangiopathy/microthrombosis
result
impaired
capillary
flow
tissue
oxygenation.
Journal of Biomedical Science,
Год журнала:
2024,
Номер
31(1)
Опубликована: Апрель 18, 2024
Abstract
Background
High
levels
of
neutrophil
extracellular
trap
(NET)
formation
or
NETosis
and
autoantibodies
are
related
to
poor
prognosis
disease
severity
COVID-19
patients.
Human
angiotensin-converting
enzyme
2
(ACE2)
cross-reactive
anti-severe
acute
respiratory
syndrome
coronavirus
spike
protein
receptor-binding
domain
(SARS-CoV-2
RBD)
antibodies
(CR
Abs)
have
been
reported
as
one
the
sources
anti-ACE2
autoantibodies.
However,
pathological
implications
CR
Abs
in
NET
remain
unknown.
Methods
In
this
study,
we
first
assessed
presence
sera
patients
with
different
by
serological
analysis.
Sera
purified
IgG
from
positive
well
a
mouse
monoclonal
Ab
(mAb
127)
that
can
recognize
both
ACE2
RBD
were
tested
for
their
influence
on
possible
mechanisms
involved
studied.
Results
An
association
between
120
was
found.
The
Abs-positive
severe
mAb
127
significantly
activated
human
leukocytes
triggered
NETosis,
RBD.
This
coexistence
RBD,
thrombus-related
cells
but
abolished
when
interaction
Fc
receptors
disrupted.
We
also
revealed
Abs-induced
suppressed
recombinant
Src
family
kinase
inhibitor,
dasatinib.
Furthermore,
found
vaccination
not
only
reduced
prevented
production
after
SARS-CoV-2
infection.
Conclusions
Our
findings
provide
pathogenic
effects
exacerbating
enhancing
highlighting
dasatinib
potential
treatments,
supporting
benefit
reducing
Memórias do Instituto Oswaldo Cruz,
Год журнала:
2025,
Номер
120
Опубликована: Янв. 1, 2025
Coronavirus
disease
2019
(COVID-19)
is
caused
by
the
new
coronavirus
2
(severe
acute
respiratory
syndrome
-
SARS-CoV-2).
Long
COVID
a
condition
associated
with
persistent
COVID-19
symptoms
and/or
emerging
symptoms.
Telomeres
are
specialised
structures
for
genome
protection
at
end
of
chromosomes
and
telomerase
enzyme
that
synthesises
telomere
DNA.
Patients
were
recruited
Pedro
Ernesto
University
Hospital
(HUPE)
in
Rio
de
Janeiro,
Brazil,
main
purpose
investigating
association
between
length
COVID.
Leukocyte
(LTL)
was
determined
quantitative
real-time
polymerase
chain
reaction
(qPCR)
34
patients
compared
to
control
group
(n
=
122).
Telomerase
activity
qPCR
assays
using
commercial
kit
from
ScienCell.
A
questionnaire
on
symptoms,
vaccine
doses
blood
count
completed.
The
found
have
an
increase
LTL.
also
examined
smaller
number
be
reactivated
blood.
It
will
necessary
conduct
further
studies
monitor
determine
if
future
health
issues
could
linked
elongated
telomeres.
INTERNATIONAL NEUROLOGICAL JOURNAL,
Год журнала:
2025,
Номер
21(2), С. 139 - 145
Опубликована: Апрель 24, 2025
Background.
COVID-19
is
associated
with
disorders
in
the
blood
coagulation
system
that
may
persist
beyond
acute
phase
of
disease,
particularly
individuals
pre-existing
cerebrovascular
conditions.
This
research
purposed
to
evaluate
changes
key
parameters
procoagulant,
anticoagulant,
and
fibrinolytic
links
hemostatic
patients
chronic
cerebral
ischemia
(CCI)
following
recovery
from
COVID-19.
Materials
methods.
The
study
involved
100
aged
43
74
years
diagnosed
CCI
divided
into
two
experimental
groups:
+
group,
which
included
60
a
history
COVID-19,
consisted
40
without
SARS-CoV-2
infection
past.
Plasma
levels
markers,
such
as
prothrombin,
protein
C,
thrombomodulin,
plasminogen,
tissue
plasminogen
activator,
activator
inhibitor-1,
von
Willebrand
factor,
were
measured
using
enzyme-linked
immunosorbent
assay.
Results.
did
not
observe
significant
differences
prothrombin
or
C
between
However,
there
was
20.9
%
increase
plasma
thrombomodulin
participants
who
had
recovered
compared
those
prior
infection.
An
inhibitor-1
content
by
19.4
found
group
while
no
its
established.
Notably,
factor
show
statistically
groups,
could
indicate
gradual
correction
endothelial
disturbances
post-COVID-19
over
time.
Conclusions.
data
obtained
complexity
CCI,
characterized
persistent
low-grade
inflammation
possible
fibrinolysis
inhibition.
At
same
time,
results
suggest
dysfunction
be
pronounced
feature
late
period.