Association of OAS1 gene polymorphism with the severity of COVID‑19 infection
Noha G. Bader El Din,
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Rehab I. Moustafa,
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Enaya Ghaleb
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et al.
World Academy of Sciences Journal,
Journal Year:
2024,
Volume and Issue:
6(6)
Published: Oct. 9, 2024
The
ongoing
coronavirus
disease
2019
(COVID‑19)
pandemic
has
underscored
the
critical
need
to
investigate
host
genetic
factors
that
may
influence
susceptibility
and
severity.
Among
these,
2'‑5'‑oligoadenylate
synthase
1
(OAS1)
single
nucleotide
polymorphism
(SNP)
rs10774671
been
implicated
in
antiviral
response
against
coronaviruses
clinical
outcomes.
aim
of
present
retrospective
study
was
association
between
OAS1
gene
severity
COVID‑19.
A
total
200
subjects
were
enrolled,
including
75
healthy
controls
125
patients
with
SNP
assessed
using
PCR‑RFLP
analysis.
findings
revealed
an
upward
trend
prevalence
allele
among
individuals,
who
developed
a
severe
course
Specifically,
17.8%
infection
carried
GG
genotype,
52.8%
had
GA
genotype
30.4%
AA
(P=0.0001).
Notably,
exclusively
detected
COVID‑19
(P<0.0001).
Moreover,
frequency
markedly
higher
than
G
Multivariate
analysis
individuals
6.8‑fold
greater
likelihood
progressing
more
(odds
ratio,
6.86;
95%
CI,
2.83‑16.63;
P<0.0001).
Thus,
holds
promise
as
potential
marker
could
be
valuable
predicting
progression
outcome
infection.
Language: Английский
OAS1 induces endothelial dysfunction and promotes monocyte adhesion through the NFκB pathway in Atherosclerosis
Miao Liang,
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Weikang Li,
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Xixi Xie
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et al.
Archives of Biochemistry and Biophysics,
Journal Year:
2024,
Volume and Issue:
763, P. 110222 - 110222
Published: Nov. 19, 2024
Language: Английский
Evaluation of Suppressor of Cytokine Signaling 1, Interleukin-29 and Lysosomal Trafficking Regulator in Severe COVID-19
Journal of Kermanshah University of Medical Sciences,
Journal Year:
2024,
Volume and Issue:
28(4)
Published: Nov. 13, 2024
Background:
The
pathogenesis
of
Severe
SARS-CoV-2
is
closely
linked
to
severe
immune
responses
and
inflammation
caused
by
the
virus.
In
this
context,
suppressor
cytokine
signaling
1
(SOCS1)
has
a
crucial
role
in
inhibiting
cytokine-induced
responses.
On
other
hand,
interleukin-29
(IL-29)
lysosomal
trafficking
regulator
(LYST)
are
important
molecules
involved
inducing
Objectives:
This
study
aimed
assess
mRNA
levels
SOCS1,
IL-29,
LYST
SARS-CoV-2-infected
patients
with
symptoms.
Methods:
cross-sectional
study,
70
infected
symptoms
healthy
controls
were
evaluated.
RNA
was
extracted
from
peripheral
blood
after
cDNA
synthesis,
assessed
Real-Time
PCR
technique
Results:
revealed
that
COVID-19
exhibited
significant
increase
IL-29
compared
individuals.
However,
there
no
observed
alterations
SOCS1
patient
group.
Conclusions:
results
emphasize
importance
as
potential
biomarker
or
therapeutic
target
for
cases.
Further
research
needed
investigate
specific
mechanisms
through
which
influences
contributes
development
disease.
Additionally,
exploring
factors
may
regulate
expression
could
provide
more
comprehensive
understanding
their
roles
pathogenesis.
Language: Английский
SARS-CoV-2 infection of human pluripotent stem cell-derived vascular cells reveals smooth muscle cells as key mediators of vascular pathology during infection
Alexsia Richards,
No information about this author
Andrew Khalil,
No information about this author
Max Friesen
No information about this author
et al.
Nature Communications,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: Dec. 30, 2024
Although
respiratory
symptoms
are
the
most
prevalent
disease
manifestation
of
infection
by
Severe
Acute
Respiratory
Syndrome
Coronavirus
2
(SARS-CoV-2),
nearly
20%
hospitalized
patients
at
risk
for
thromboembolic
events.
This
prothrombotic
state
is
considered
a
key
factor
in
increased
stroke,
which
observed
clinically
during
both
acute
and
long
after
clear.
Here,
we
develop
model
SARS-CoV-2
using
human-induced
pluripotent
stem
cell-derived
endothelial
cells
(ECs),
pericytes
(PCs),
smooth
muscle
(SMCs)
to
recapitulate
vascular
pathology
associated
with
exposure.
Our
results
demonstrate
that
perivascular
cells,
particularly
SMCs,
susceptible
target
infection.
Utilizing
RNA
sequencing,
characterize
transcriptomic
changes
accompanying
PCs,
ECs.
We
observe
infected
SMCs
shift
pro-inflammatory
increase
expression
mediators
coagulation
cascade.
Further,
show
human
ECs
exposed
secretome
produce
hemostatic
factors
contribute
dysfunction
despite
not
being
direct
The
findings
here
observations
from
patient
sera
COVID-19
provide
mechanistic
insight
into
unique
implications
cellular
level.
Language: Английский
SARS-CoV-2 infection of human pluripotent stem cell-derived vascular cells reveals smooth muscle cells as key mediators of vascular pathology during infection
Alexsia Richards,
No information about this author
Andrew Khalil,
No information about this author
Max Friesen
No information about this author
et al.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2023,
Volume and Issue:
unknown
Published: Aug. 7, 2023
Abstract
Although
respiratory
symptoms
are
the
most
prevalent
disease
manifestation
of
infection
by
Severe
Acute
Respiratory
Syndrome
Coronavirus
2
(SARS-CoV-2),
nearly
20%
hospitalized
patients
at
risk
for
thromboembolic
events.
This
prothrombotic
state
is
considered
a
key
factor
in
increased
stroke,
which
observed
clinically
during
both
acute
and
long
after
clear.
Here
we
develop
model
SARS-CoV-2
using
human-induced
pluripotent
stem
cell-derived
endothelial
cells
(ECs),
pericytes
(PCs),
smooth
muscle
(SMCs)
to
recapitulate
vascular
pathology
associated
with
exposure.
Our
results
demonstrate
that
perivascular
cells,
particularly
SMCs,
susceptible
target
infection.
Utilizing
RNA
sequencing,
characterize
transcriptomic
changes
accompanying
PCs,
ECs.
We
observe
infected
SMCs
shift
pro-inflammatory
increase
expression
mediators
coagulation
cascade.
Further,
show
human
ECs
exposed
secretome
produce
hemostatic
factors
contribute
dysfunction,
despite
not
being
direct
The
findings
here
observations
from
patient
sera
COVID-19
provide
mechanistic
insight
into
unique
implications
cellular
level.
Language: Английский