Briefings in Functional Genomics,
Journal Year:
2023,
Volume and Issue:
23(4), P. 349 - 362
Published: Nov. 20, 2023
Abstract
The
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
and
disease
2019
(COVID-19)
have
been
around
for
more
than
3
years
now.
However,
due
to
constant
viral
evolution,
novel
variants
are
emerging,
leaving
old
treatment
protocols
redundant.
As
options
dwindle,
infection
rates
continue
rise
seasonal
surges
become
progressively
common
across
the
world,
rapid
solutions
required.
With
genomic
proteomic
methods
generating
enormous
amounts
of
data
expand
our
understanding
SARS-CoV-2
biology,
there
is
an
urgent
requirement
development
therapeutic
that
can
allow
translational
research
flourish.
In
this
review,
we
highlight
current
state
COVID-19
in
world
effects
post-infection
sequelae.
We
present
contribution
COVID-19,
with
various
approaches,
including
antivirals,
monoclonal
antibodies
vaccines,
as
well
alternate
such
immunomodulators,
currently
being
studied
reiterate
importance
strategies
contain
COVID-19.
Frontiers in Bioengineering and Biotechnology,
Journal Year:
2025,
Volume and Issue:
13
Published: March 12, 2025
The
advent
of
mRNA
vaccines,
accelerated
by
the
global
response
to
COVID-19
pandemic,
marks
a
transformative
shift
in
vaccine
technology.
In
this
article,
we
discuss
development,
current
applications,
and
prospects
vaccines
for
both
prevention
treatment
infectious
diseases
oncology.
By
leveraging
capacity
encode
antigens
within
host
cells
directly,
provide
versatile
scalable
platform
suitable
addressing
broad
spectrum
pathogens
tumor-specific
antigens.
We
highlight
recent
advancements
design,
innovative
delivery
mechanisms,
ongoing
clinical
trials,
with
particular
emphasis
on
their
efficacy
combating
diseases,
such
as
COVID-19,
Zika,
influenza,
well
emerging
potential
cancer
immunotherapy.
also
address
critical
challenges,
including
stability,
optimization
immune
responses,
broader
issue
accessibility.
Finally,
review
strategies
advancing
next-generation
aim
overcoming
limitations
technology
enhancing
preventive
therapeutic
approaches
oncological
diseases.
Pharmaceuticals,
Journal Year:
2023,
Volume and Issue:
16(6), P. 904 - 904
Published: June 20, 2023
The
gut
microbiota
play
a
crucial
role
in
maintaining
host
health
and
have
significant
impact
on
human
disease.
In
this
study,
we
investigated
the
alpha
diversity
of
COVID-19
patients
analyzed
variants,
antibiotic
treatment,
type
2
diabetes
(T2D),
metformin
therapy
composition
diversity.
We
used
culture-based
method
to
analyze
calculated
alpha-diversity
using
Shannon
H'
Simpson
1/D
indices.
collected
clinical
data,
such
as
length
hospital
stay
(LoS),
C-reactive
protein
(CRP)
levels,
neutrophil-to-lymphocyte
ratio.
found
that
with
T2D
had
significantly
lower
than
those
without
T2D.
Antibiotic
use
was
associated
reduction
alpha-diversity,
while
an
increase.
did
not
find
differences
between
Delta
Omicron
groups.
stay,
CRP
NLR
showed
weak
moderate
correlations
Our
findings
suggest
diverse
may
benefit
Interventions
preserve
or
restore
diversity,
avoiding
unnecessary
use,
promoting
therapy,
incorporating
probiotics,
improve
patient
outcomes.
Viruses,
Journal Year:
2024,
Volume and Issue:
16(1), P. 112 - 112
Published: Jan. 12, 2024
This
study
investigates
the
intricate
interplay
between
Metabolic-associated
Fatty
Liver
Disease
(MAFLD)
and
COVID-19,
exploring
impact
of
MAFLD
on
disease
severity,
outcomes,
efficacy
antiviral
agent
Paxlovid
(nirmatrelvir/ritonavir).
MAFLD,
affecting
a
quarter
global
population,
emerges
as
potential
risk
factor
for
severe
yet
underlying
pathophysiological
mechanisms
remain
elusive.
focuses
clinical
significance
Paxlovid,
first
orally
bioavailable
granted
Emergency
Use
Authorization
in
United
States.
Notably,
outcomes
from
phase
II/III
trials
exhibit
an
88%
relative
reduction
COVID-19-associated
hospitalization
or
mortality
among
high-risk
patients.
Despite
conflicting
data
association
COVID-19
this
research
strives
to
bridge
gap
by
evaluating
effectiveness
patients
with
addressing
scarcity
relevant
studies.
Frontiers in Genetics,
Journal Year:
2024,
Volume and Issue:
15
Published: Sept. 4, 2024
This
study
investigated
the
influence
of
single
nucleotide
polymorphisms
(SNPs)
in
genes
associated
with
interferon
pathway
(IFNAR2
rs2236757),
antiviral
response
(OAS1
rs10774671,
OAS3
rs10735079),
and
viral
entry
(ACE2
rs2074192)
on
COVID-19
severity
their
association
nonalcoholic
fatty
liver
disease
(MAFLD).
We
did
not
observe
a
significant
between
SNPs
severity.
While
IFNAR2
rs2236757
A
allele
was
correlated
higher
creatinine
levels
upon
admission
G
lower
band
neutrophils
discharge,
these
findings
require
further
investigation.
The
distribution
OAS
gene
(rs10774671
rs10735079)
differ
MAFLD
patients
non-MAFLD
patients.
Our
population's
ACE2
rs2074192
genotypes
alleles
differed
from
that
European
reference
population.
Overall,
our
suggest
specific
may
be
major
contributors
to
patient
population,
highlighting
potential
role
other
genetic
factors
environmental
influences.
Viruses,
Journal Year:
2023,
Volume and Issue:
15(8), P. 1724 - 1724
Published: Aug. 12, 2023
Metabolic-associated
fatty
liver
disease
(MAFLD)
and
its
potential
impact
on
the
severity
of
COVID-19
have
gained
significant
attention
during
pandemic.
This
review
aimed
to
explore
genetic
determinants
associated
with
MAFLD,
previously
recognized
as
non-alcoholic
(NAFLD),
their
influence
outcomes.
Various
polymorphisms,
including
PNPLA3
(rs738409),
GCKR
(rs780094),
TM6SF2
(rs58542926),
LYPLAL1
(rs12137855),
been
investigated
in
relation
MAFLD
susceptibility
progression.
Genome-wide
association
studies
meta-analyses
revealed
associations
between
these
variants
risk,
well
effects
lipid
metabolism,
glucose
regulation,
function.
Furthermore,
emerging
evidence
suggests
a
possible
connection
MAFLD-associated
polymorphisms
COVID-19.
Studies
exploring
indicated
outcomes
shown
conflicting
results.
Some
observed
protective
effect
certain
against
severe
COVID-19,
while
others
reported
no
associations.
highlights
importance
understanding
implications
for
Further
research
is
needed
elucidate
precise
mechanisms
linking
develop
gene
profiling
tools
early
prediction
If
confirmed
severity,
could
aid
identification
high-risk
individuals
improving
management
Viruses,
Journal Year:
2024,
Volume and Issue:
16(6), P. 985 - 985
Published: June 19, 2024
Metabolic-associated
fatty
liver
disease
(MAFLD)
is
a
risk
factor
for
severe
COVID-19.
This
study
explores
the
potential
influence
of
gut
hormone
receptor
and
immune
response
gene
expression
on
COVID-19
outcomes
in
MAFLD
patients.
Frontiers in Pediatrics,
Journal Year:
2025,
Volume and Issue:
13
Published: Feb. 24, 2025
Recent
studies
have
underscored
the
importance
of
genetic
factors
in
predicting
COVID-19
susceptibility
and
severity.
While
cytokine
storms
are
crucial
disease
severity,
predisposition
significantly
influences
immune
responses.
Our
study
examined
genes
related
to
SARS-CoV-2
invasion
(ACE2
rs2074192)
interferon-induced
immunity
(IFNAR2
rs2236757,
TYK2
rs2304256,
OAS1
rs10774671,
OAS3
rs10735079).
Additionally,
we
investigated
linked
Kawasaki
(CD40
rs4813003,
FCGR2A
rs1801274,
CASP3
rs113420705)
that
play
roles
immunogenesis.
The
pilot
study,
which
involved
75
pediatric
patients
aged
one
month
17
years
[43
with
active
COVID-19,
children
multisystem
inflammatory
syndrome
(MIS-C),
15
healthy
controls],
was
conducted
Ternopil,
Ukraine.
Gene
polymorphism
studied
for
all
patients.
ELISA
kits
were
used
interleukin
studies,
including
Human
IL-1β
(Interleukin
1
Beta),
IL-6
6),
IL-8
8),
IL-12
12),
IFN-α
(Interferon
Alpha),
TNF-α
(Tumor
Necrosis
Factor
Alpha).
Statistical
analysis
performed
using
IBM
SPSS
Statistics
21
GraphPad
Prism
8.4.3.
identified
significant
gene-cytokine
associations
ACE2
rs2074192
T
allele
correlated
increased
IL-1β,
IL-6,
IL-8,
TNF-α.
IFNAR2
rs2236757
A
elevated
levels
low
levels,
while
rs10774671
carriers
also
exhibited
lower
levels.
prognostically
determining
infected
SARS-CoV-2.
gene
rs10735079
associated
changes
precisely
a
high
level.
CD40
rs4813003
C
had
higher
IL-12.
results
our
revealed
correlation
between
rs1801274
(A/G).
rs113420705
led
an
increase
IL-6.
These
findings
enhance
understanding
may
hold
promise
developing
targeted
interventions
providing
personalized
medical
approach
each
patient.
Virology Journal,
Journal Year:
2025,
Volume and Issue:
22(1)
Published: April 10, 2025
To
develop
an
adequate
system
for
assessing
the
duration
of
IFN
antiviral
activity
in
nasal
cavity
animals
and
to
study
a
new
drug
form
gel
comparison
with
known
spray
form.
assess
specific
IFN,
drugs
were
administered
into
experimental
rats.
One,
3,
4
h
after
administration,
cavities
rats
washed
out,
from
(WNC)
was
analyzed
vitro.
Developed
algorithm
preparations
using
sensitive
vitro
test
system,
which
analysis
WNC
made
it
possible
detect
administration
forms
IFN-a
variant
spray.
It
established
that
1
intranasal
same
concentration
is:
266.8
±
14.0
IU/ml
IFN/spray
260.2
20.9
IU/
ml
IFN/gel.
Three
hours
are
administered,
their
decreases
but
remains
at
sufficiently
high
level:
121.4
5.4
88.3
6.2
Four
IFN/gel
significantly
greater
than
IFN/spray:
39.4
4.9
10.6
1.0
IU/ml,
respectively.
The
developed
evaluating
allows
local
effect
drugs.
persisted
administration:
on
walls
Viruses,
Journal Year:
2023,
Volume and Issue:
15(10), P. 2093 - 2093
Published: Oct. 14, 2023
Coronavirus
disease
(COVID-19)
and
its
outcomes
remain
one
of
the
most
challenging
problems
today.
COVID-19
in
children
could
be
asymptomatic,
but
can
result
a
fatal
outcome;
therefore,
predictions
severity
are
important.
The
goal
was
to
investigate
human
genetic
factors
that
associated
with
children.
Single-nucleotide
polymorphisms
following
genes
were
studied:
ACE2
(rs2074192),
IFNAR2
(rs2236757),
TYK2
(rs2304256),
OAS1
(rs10774671),
OAS3
(rs10735079),
CD40
(rs4813003),
FCGR2A
(rs1801274)
CASP3
(rs113420705).
In
case-control
study
30
mild
or
moderate
course
disease;
severe
symptoms
multisystem
inflammatory
syndrome
(MIS-C)
15
who
healthy,
did
not
have
SARS-CoV-2
(PCR
negative,
Ig
G
negative).
revealed
rs2074192
(allele
T),
rs2236757
A),
rs10774671
rs4813003
C),
rs113420705
C)
male
sex
contribute
MIS-C
85.6%
cases.
World
Health
Organization
reported
new
variants
may
cause
previously
unseen
Although
has
limitations
due
cohort
size,
findings
help
provide
better
understanding
infection
proactive
pediatric
patient
management.
Metabolic-associated
fatty
liver
disease
(MAFLD)
is
a
risk
factor
for
severe
COVID-19.
This
study
explores
the
potential
influence
of
gut
hormone
receptor
and
immune
response
gene
expression
on
COVID-19
outcomes
in
MAFLD
patients.
Methods:
We
investigated
levels
AHR,
FFAR2,
FXR,
TGR5
patients
with
compared
to
controls.
examined
associations
between
clinical
outcomes.
Results:
displayed
altered
AHR
expression,
potentially
impacting
recovery.
Downregulated
correlated
increased
coagulation
parameters.
Elevated
FFAR2
linked
specific
cell
populations
hospital
stay
duration.
Significantly
lower
FXR
was
observed
both
Conclusion:
Our
findings
suggest
modulatory
roles
MAFLD.