Frontiers in Cellular and Infection Microbiology,
Год журнала:
2023,
Номер
13
Опубликована: Окт. 30, 2023
Objective
The
Omicron
BA.5.2
variant
of
SARS-CoV-2
has
undergone
several
evolutionary
adaptations,
leading
to
multiple
subvariants.
Rapid
and
accurate
characterization
these
subvariants
is
essential
for
effective
treatment,
particularly
in
critically
ill
patients.
This
study
leverages
Next-Generation
Sequencing
(NGS)
elucidate
the
clinical
immunological
features
across
different
Methods
We
enrolled
28
patients
infected
with
variant,
hospitalized
Zhangjiajie
People’s
Hospital,
Hunan,
China,
between
January
20,
2023,
March
31,
2023.
Throat
swabs
were
collected
upon
admission
NGS-based
identification
Clinical
data,
including
qSOFA
scores
key
laboratory
tests,
collated.
A
detailed
analysis
lymphocyte
subsets
was
conducted
ascertain
extent
immune
cell
damage
disease
severity.
Results
Patients
various
subvariants,
BA.5.2.48,
BA.5.2.49,
BA.5.2.6,
BF.7.14,
DY.1,
DY.2,
DY.3,
DY.4.
Despite
having
43
identical
mutation
sites,
each
subvariant
exhibited
unique
marker
mutations.
Critically
demonstrated
significant
depletion
total
count,
T
cells,
CD4,
CD8,
B
NK
cells
(
P
<
0.05
).
However,
there
no
differences
markers
Conclusion
reveals
that
experience
similar
levels
cellular
dysfunction
inflammatory
response.
Four
mutations
-
ORF1a:K3353R,
ORF1a:L3667F,
ORF1b:S997P,
S:T883I
showed
correlation
responses
although
this
conclusion
suffers
from
small
sample
size.
Our
findings
underscore
utility
NGS
comprehensive
assessment
infectious
diseases,
contributing
more
decision-making.
International Journal of Molecular Sciences,
Год журнала:
2023,
Номер
24(19), С. 14876 - 14876
Опубликована: Окт. 4, 2023
SARS-CoV-2
infection,
discovered
and
isolated
in
Wuhan
City,
Hubei
Province,
China,
causes
acute
atypical
respiratory
symptoms
has
led
to
profound
changes
our
lives.
COVID-19
is
characterized
by
a
wide
range
of
complications,
which
include
pulmonary
embolism,
thromboembolism
arterial
clot
formation,
arrhythmias,
cardiomyopathy,
multiorgan
failure,
more.
The
disease
caused
worldwide
pandemic,
despite
various
measures
such
as
social
distancing,
preventive
strategies,
therapeutic
approaches,
the
creation
vaccines,
novel
coronavirus
infection
(COVID-19)
still
hides
many
mysteries
for
scientific
community.
Oxidative
stress
been
suggested
play
an
essential
role
pathogenesis
COVID-19,
determining
free
radical
levels
patients
with
may
provide
insight
into
severity.
generation
abnormal
oxidants
under
COVID-19-induced
cytokine
storm
irreversible
oxidation
macromolecules
subsequent
damage
cells,
tissues,
organs.
Clinical
studies
have
shown
that
oxidative
initiates
endothelial
damage,
increases
risk
complications
post-COVID-19
or
long-COVID-19
cases.
This
review
describes
radicals
mediation
mitochondrial
dysfunction.
Clinical Pharmacology Advances and Applications,
Год журнала:
2024,
Номер
Volume 16, С. 1 - 25
Опубликована: Янв. 1, 2024
The
Severe
Acute
Respiratory
Syndrome
Coronavirus
2
(SARS-CoV-2)
is
a
betacoronavirus
responsible
for
the
COVID-19
pandemic,
causing
respiratory
disorders,
and
even
death
in
some
individuals,
if
not
appropriately
treated
time.
To
face
preventive
measures
have
been
taken
against
contagions
application
of
vaccines
to
prevent
severe
disease
cases.
For
treatment,
antiviral,
antiparasitic,
anticoagulant
other
drugs
reused
due
limited
specific
medicaments
disease.
Drug
repurposing
an
emerging
strategy
with
therapies
that
already
tested
safe
humans.
One
promising
alternative
systematic
experimental
screening
vast
pool
compounds
computational
drug
(in
silico
assay).
Using
these
tools,
new
uses
approved
such
as
chloroquine,
hydroxychloroquine,
ivermectin,
zidovudine,
ribavirin,
lamivudine,
remdesivir,
lopinavir
tenofovir/emtricitabine
conducted,
showing
effectiveness
vitro
SARS-CoV-2
these,
also
clinical
trials.
Additionally,
therapeutic
options
sought
natural
products
(terpenoids,
alkaloids,
saponins
phenolics)
results
use
Among
most
studied
are
resveratrol,
quercetin,
hesperidin,
curcumin,
myricetin
betulinic
acid,
which
were
proposed
inhibitors.
control
SARS-CoV2,
better
observed
remdesivir
hospitalized
patients
outpatients.
Regarding
products,
quercetin
demonstrated
antiviral
activity
vivo,
nebulized
formulation
has
alleviate
symptoms
COVID-19.
This
review
shows
evidence
efficacy
potential
treatment
this,
search
was
carried
out
PubMed,
SciELO
ScienceDirect
databases
articles
about
or
under
study
recognized
their
SARS-CoV-2.
Frontiers in Cellular and Infection Microbiology,
Год журнала:
2024,
Номер
14
Опубликована: Май 28, 2024
The
novel
coronavirus
disease
2019
(COVID-19)
pandemic
outbreak
caused
by
severe
acute
respiratory
syndrome
coronavirus-2
(SARS-CoV-2)
has
garnered
unprecedented
global
attention.
It
over
2.47
million
deaths
through
various
syndromes
such
as
distress,
hypercoagulability,
and
multiple
organ
failure.
viral
invasion
proceeds
the
ACE2
receptor,
expressed
in
cell
types,
some
patients
serious
damage
to
tissues,
organs,
immune
cells,
microbes
that
colonize
gastrointestinal
tract
(GIT).
Some
who
survived
SARS-CoV-2
infection
have
developed
months
of
persistent
long-COVID-19
symptoms
or
post-acute
sequelae
COVID-19
(PASC).
Diagnosis
these
revealed
biological
effects,
none
which
are
mutually
exclusive.
However,
severity
also
depends
on
numerous
comorbidities
obesity,
age,
diabetes,
hypertension
care
must
be
taken
with
respect
other
morbidities,
host
immunity.
Gut
microbiota
relation
immunopathology
is
considered
evolve
progression
via
mechanisms
biochemical
metabolism,
exacerbation
inflammation,
intestinal
mucosal
secretion,
cytokine
storm,
immunity
regulation.
Therefore,
modulation
gut
microbiome
equilibrium
food
supplements
probiotics
remains
a
hot
topic
current
research
debate.
In
this
review,
we
discuss
complications
physio-pathological
effects
infection,
GIT
response,
therapeutic
pharmacological
strategies.
We
summarize
targets
probiotics,
their
limitations,
efficacy
preclinical
clinical
drugs
effectively
inhibit
spread
SARS-CoV-2.
Journal of Clinical Medicine,
Год журнала:
2023,
Номер
12(12), С. 4057 - 4057
Опубликована: Июнь 15, 2023
All
severe
cases
of
SARS-CoV-2
infections
are
characterized
by
a
high
risk
disease
progression
towards
ARDS,
leading
to
bad
outcome.
Respiratory
symptoms
in
COVID-19
patients
often
do
not
correspond
disease's
worsening.
In
our
sample,
median
age
was
74
years
(72-75)
and
54%
were
men.
The
period
hospitalization
9
days.
Firstly,
we
observed
significant
asynchronous
trend
neutrophil-to-lymphocyte
ratio
(NLR)
C-reactive
protein
(CRP)
764
selected
among
963
patients,
who
consecutively
recruited
two
hospitals
(Cannizzaro,
S.
Marco)
Catania,
Italy.
NLR
values
deceased
showed
an
increase
from
baseline
over
time.
By
contrast,
CRP
tended
fall
day
all
three
subgroups,
but
steeply
increased
at
the
end
only
ICU-admitted
patients.
Then,
evaluated
relationships
between
as
continuous
variables
with
PaO2/FiO2
(P/F).
independent
predictor
mortality
(HR:
1.77,
p
<
0.0001),
while
ICU
admission
more
significantly
associated
1.70,
0.0001).
Finally,
age,
neutrophils,
CRP,
lymphocytes
directly
linked
P/F,
influence
inflammation
on
reflected
also
mediated
neutrophils.
Antibodies,
Год журнала:
2024,
Номер
13(1), С. 13 - 13
Опубликована: Фев. 8, 2024
The
COVID-19
pandemic
caused
by
Severe
Acute
Respiratory
Syndrome
Coronavirus
2
(SARS-CoV-2)
has
led
to
almost
seven
million
deaths
worldwide.
SARS-CoV-2
causes
infection
through
respiratory
transmission
and
can
occur
either
without
any
symptoms
or
with
clinical
manifestations
which
be
mild,
severe
or,
in
some
cases,
even
fatal.
Innate
immunity
provides
the
initial
defense
against
virus
sensing
pathogen-associated
molecular
patterns
triggering
signaling
pathways
that
activate
antiviral
inflammatory
responses,
limit
viral
replication
help
identification
removal
of
infected
cells.
However,
temporally
dysregulated
excessive
activation
innate
immune
response
is
deleterious
for
host
associates
COVID-19.
In
addition
its
defensive
role,
pivotal
priming
adaptive
polarizing
effector
function.
This
capacity
relevant
context
both
natural
vaccination.
Here,
we
provide
an
overview
current
knowledge
responses
Acute
lung
injury
(ALI)
is
a
severe
condition
often
seen
in
intensive
care
unit
patients.
Due
to
limited
treatment
options,
ALI
linked
high
rates
of
mortality
and
morbidity.
Bacterial
viral
infections
are
significant
contributors
ALI.
For
instance,
acute
respiratory
syndrome-coronavirus-2
(SARS-CoV-2)
infection
can
lead
strong
inflammatory
response
that
may
progress
ALI,
leading
cause
death
COVID-19
cases.
Prior
research
has
demonstrated
sulfonamides
sydnones
exhibit
anti-inflammatory
antiviral
properties,
which
led
us
develop
compounds
containing
both
scaffolds.
Most
the
new
sulfonamide-sydnone
hybrids
expected
be
orally
bioavailable
based
on
silico
ADME
predictions.
They
effectively
suppressed
development
lipopolysaccharide
(LPS)-challenged
mice
inhibited
replication
Calu-3
cells,
with
minimal
cytotoxicity
non-infected
Vero
E6
cells.
Molecular
docking
investigations
indicated
some
possible
targets
for
action
sydnones,
highlighting
interaction
non-structural
proteins
SARS-CoV-2.
Additionally,
combined
experimental
theoretical
studies
strongly
interact
human
serum
albumin,
suggesting
extended
residence
time
bloodstream.
COVID-19
appears
to
have
a
progression
of
three
stages.
The
latter
stage
is
characterized
by
high
level
cytokine
release,
which
in
turn
triggers
an
uncontrolled
reaction
known
as
storm
where
mast
cells
are
involved.
presence
anti-IgE
antibodies
against
SARS-CoV-2
this
phase
has
been
previously
reported,
suggesting
association
with
the
severity
disease.
Our
study
aims
assess
prognostic
significance
IgE
across
spectrum
clinical
presentations,
including
individual
mild
symptoms,
hospitalized
patients,
and
those
who
presented
critical
progression.
included
64
patients
distributed
into
following
groups:
22
critically
ill
individuals
(Critical);
21
non-critical
(Severe);
symptomatic
non-hospitalized
cases
(Mild);
healthy
blood
donors
samples
collected
October
2019.
Anti-IgE
Spike
(S)
protein
were
detected
using
homemade
ELISA,
plate
was
sensitized
RBD
recombinant
S
protein.
Among
infected
28.1%
tested
positive
for
isotype
RBD,
whose
prevalence
similar
Mild
23.8%,
Severe
28.6%,
Critical
31.8%
(p
=
0.842).
Patients
response
exhibited
higher
levels
LDH
compared
non-IgE
responders,
40%
increase
0.037),
non-significantly
tendency
other
inflammatory
markers.
In
infection,
roughly
fourth
response,
regardless
disease
severity,
associated
LDH.
All
severe
cases
of
SARS-CoV-2
infections
are
characterized
by
a
high
risk
disease
progression
towards
ARDS,
leading
to
bad
outcome.
Respiratory
symptoms
in
COVID-19
patients
often
do
not
correspond
disease’s
worsening.
A
dysregulated
host
response
the
large
viral
load
could
play
key
role
progression.
In
our
sample
median
age
was
74
years
(72-75)
and
54%
were
men.
Median
period
hospitalization
9
days.
Firstly,
we
observed
an
asynchronous
trend
neutrophil-to-lymphocyte
ratio
(NLR)
C-reactive
protein
(CRP)
764
selected
among
963
who
consecutively
recruited
two
hospitals
(Cannizzaro,
S.
Marco)
Catania,
Italy.
NLR
values
deceased
showed
increase
from
baseline
over
time.
By
contrast,
CRP
tended
fall
day
all
four
subgroups,
but
steeply
increased
at
end
only
ICU-admitted
patients.
Then
evaluated
relationships
between
as
continuous
variables
with
PaO2/FiO2
(P/F).
Finally,
made
mediation
moderation
analyses
determine
link
inflammation
(CRP),
immune
system
(neutrophils
lymphocytes)
respiratory
failure
CRP,
neutrophils
P/F
linked
same
pathogenetic
chain
failure.
Vaccines,
Год журнала:
2024,
Номер
12(8), С. 921 - 921
Опубликована: Авг. 16, 2024
Coronavirus
disease
2019
(COVID-19),
caused
by
severe
acute
respiratory
syndrome
coronavirus-2
(SARS-CoV-2),
emerged
as
a
global
outbreak
in
2019,
profoundly
affecting
both
human
health
and
the
economy.
Various
vaccine
modalities
were
developed
commercialized
to
overcome
this
challenge,
including
inactivated
vaccines,
mRNA
adenovirus
vector-based
subunit
vaccines.
While
intramuscular
vaccines
induce
high
IgG
levels,
they
often
fail
stimulate
significant
mucosal
immunity
system.
We
employed
Newcastle
virus
(NDV)
vector
expressing
spike
protein
of
SARS-CoV-2
Beta
variant
(rK148/beta-S),
evaluated
efficacy
intranasal
vaccination
with
rK148/beta-S
K18-hACE2
transgenic
mice.
Intranasal
low
dose
(10