Frontiers in Immunology,
Journal Year:
2021,
Volume and Issue:
12
Published: Nov. 3, 2021
COVID-19
pandemic
remains
an
on-going
global
health
and
economic
threat
that
has
amassed
millions
of
deaths.
Severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
is
the
etiological
agent
this
disease
constantly
under
evolutionary
pressures
drive
modification
its
genome
which
may
represent
a
to
efficacy
current
vaccines
available.
This
article
highlights
facilitate
rise
new
SARS-CoV-2
variants
key
mutations
viral
spike
protein
–
L452R,
E484K,
N501Y
D614G–
promote
immune
escape
mechanism
warrant
cautionary
point
for
clinical
public
responses
in
terms
re-infection,
vaccine
breakthrough
infection
therapeutic
values.
mSphere,
Journal Year:
2021,
Volume and Issue:
6(4)
Published: Aug. 11, 2021
Reducing
the
mortality
and
morbidity
associated
with
COVID-19
remains
a
global
health
priority.
Vaccines
have
proven
highly
effective
at
preventing
infection
hospitalization,
but
efforts
must
continue
to
improve
treatment
options
for
those
who
still
become
seriously
ill.
Biomedicines,
Journal Year:
2022,
Volume and Issue:
10(6), P. 1339 - 1339
Published: June 7, 2022
Viruses
and
their
hosts
have
coevolved
for
a
long
time.
This
coevolution
places
both
the
pathogen
human
immune
system
under
selective
pressure;
on
one
hand,
has
evolved
to
combat
viruses
virally
infected
cells,
while
developed
sophisticated
mechanisms
escape
recognition
destruction
by
system.
SARS-CoV-2,
that
is
causing
current
COVID-19
pandemic,
shown
remarkable
ability
antibody
neutralization,
putting
vaccine
efficacy
at
risk.
One
of
virus’s
evasion
strategies
mitochondrial
sabotage:
reactive
oxygen
species
(ROS)
production,
physiology
impaired,
interferon
antiviral
response
suppressed.
Seminal
studies
identified
an
intra-cytoplasmatic
pathway
viral
infection,
which
occurs
through
construction
tunneling
nanotubes
(TNTs),
hence
enhancing
infection
avoiding
surveillance.
Another
method
evading
monitoring
disruption
antigen
presentation.
In
this
scenario,
SARS-CoV-2
reduces
MHC-I
molecule
expression:
SARS-CoV-2’s
open
reading
frames
(ORF
6
ORF
8)
produce
proteins
specifically
downregulate
molecules.
All
these
are
also
exploited
other
elude
detection
should
be
studied
in
depth
improve
effectiveness
future
treatments.
Compared
Wuhan
strain
or
Delta
variant,
Omicron
mutations
impaired
its
generate
syncytia,
thus
reducing
pathogenicity.
Conversely,
allowed
it
neutralization
preventing
cellular
recognition,
making
most
contagious
evasive
variant
date.
Journal of Cellular and Molecular Medicine,
Journal Year:
2022,
Volume and Issue:
26(10), P. 3022 - 3030
Published: April 13, 2022
Infection
with
the
novel
severe
acute
respiratory
syndrome
coronavirus-2
(SARS-CoV-2)
and
associated
coronavirus
disease-19
(COVID-19)
might
affect
red
blood
cells
(RBC);
possibly
altering
oxygen
supply.
However,
investigations
of
cell
morphology
RBC
rheological
parameters
during
a
mild
disease
course
are
lacking
thus,
aim
study.
Fifty
individuals
COVID-19
process
were
tested
after
phase
SARS-CoV-2
infection
(37males/13
females),
data
compared
to
n
=
42
healthy
controls
(30
males/12
females).
Analysis
venous
samples,
taken
at
rest,
revealed
higher
percentage
permanently
elongated
membrane
extensions
in
patients.
Haematological
haemoglobin
concentration,
MCH
MCV
particular,
highly
altered
COVID-19.
deformability
under
an
osmotic
gradient
significantly
reduced
Higher
RBC-NOS
activation
was
not
capable
least
part
counteract
these
reductions.
Impaired
also
be
related
morphological
changes
and/or
increased
oxidative
state.
aggregation
index
remained
unaffected.
shear
rates
necessary
balance
aggregation-disaggregation
patients
which
be,
among
others,
changes.
The
suggest
prolonged
modifications
system
even
course.
Frontiers in Immunology,
Journal Year:
2022,
Volume and Issue:
13
Published: April 21, 2022
Host
cholesterol
metabolism
remodeling
is
significantly
associated
with
the
spread
of
human
pathogenic
coronaviruses,
suggesting
virus-host
relationships
could
be
affected
by
cholesterol-modifying
drugs.
Cholesterol
has
an
important
role
in
coronavirus
entry,
membrane
fusion,
and
pathological
syncytia
formation,
therefore
metabolic
mechanisms
may
promising
drug
targets
for
infections.
Moreover,
its
metabolizing
enzymes
or
corresponding
natural
products
exert
antiviral
effects
which
are
closely
individual
viral
steps
during
replication.
Furthermore,
disease
2019
(COVID-19)
caused
severe
acute
respiratory
syndrome
2
infections
clinically
significant
low
levels,
function
as
a
potential
marker
monitoring
infection
status.
Therefore,
weaponizing
dysregulation
against
effective
strategy.
In
this
review,
we
comprehensively
review
literature
to
clarify
how
coronaviruses
exploit
host
accommodate
replication
requirements
interfere
immune
responses.
We
also
focus
on
targeting
homeostasis
critical
infection.
JAMA Network Open,
Journal Year:
2022,
Volume and Issue:
5(4), P. e227970 - e227970
Published: April 19, 2022
Importance
During
the
COVID-19
pandemic,
urgent
clinical
management
of
patients
has
mainly
included
drugs
currently
administered
for
other
diseases,
referred
to
as
repositioned
drugs.
As
a
result,
some
these
have
proved
be
not
only
ineffective
but
also
harmful
because
adverse
events
associated
with
drug-drug
interactions
(DDIs).
Objective
To
identify
DDIs
that
led
outcomes
and/or
drug
reactions
in
by
systematically
reviewing
literature
and
assessing
value
interaction
checkers
identifying
such
events.
Evidence
Review
After
identification
used
during
Drugs.com,
Drug
Interactions,
LexiComp,
Medscape,
WebMD
were
consulted
analyze
theoretical
DDI-associated
from
March
1,
2020,
through
February
28,
2022.
A
systematic
review
was
performed
searching
databases
PubMed,
Scopus,
Cochrane
articles
published
2022,
retrieve
describing
actual
DDIs.
The
again
evaluate
their
potential
assess
Findings
identified
reviewed
involved
46
different
In
total,
575
58
pairs
(305
at
least
1
reaction)
reported.
most
lopinavir
ritonavir.
Of
6917
studies,
20
met
inclusion
criteria.
These
which
enrolled
1297
overall,
reported
115
DDI-related
events:
15
(26%)
identifiable
all
tools
analyzed,
29
(50%)
them,
14
(24%)
remained
nonidentifiable.
Conclusions
Relevance
main
finding
this
is
use
could
several
reactions,
including
severe
life-threatening
Both
between
treat
those
already
should
evaluated.
Journal of Medicinal Chemistry,
Journal Year:
2023,
Volume and Issue:
66(6), P. 3664 - 3702
Published: March 1, 2023
The
most
advanced
antiviral
molecules
addressing
major
SARS-CoV-2
targets
(Main
protease,
Spike
protein,
and
RNA
polymerase),
compared
with
proteins
of
other
human
pathogenic
coronaviruses,
may
have
a
short-lasting
clinical
efficacy.
Accumulating
knowledge
on
the
mechanisms
underlying
target
structural
basis,
its
mutational
progression,
related
biological
significance
to
virus
replication
allows
envisaging
development
better-targeted
therapies
in
context
COVID-19
epidemic
future
coronavirus
outbreaks.
identification
evolutionary
patterns
based
solely
sequence
information
analysis
for
those
can
provide
meaningful
insights
into
molecular
basis
host–pathogen
interactions
adaptation,
leading
drug
resistance
phenomena.
Herein,
we
will
explore
how
study
observed
predicted
mutations
offer
valuable
suggestions
application
so-called
“synthetic
lethal”
strategy
Main
protease
protein.
synergy
between
genetics
evidence
discovery
prioritize
novel
long-lasting
agents.
International Journal of Molecular Sciences,
Journal Year:
2023,
Volume and Issue:
24(10), P. 8945 - 8945
Published: May 18, 2023
Since
the
first
description
of
COVID-19
infection,
among
clinical
manifestations
disease,
including
fever,
dyspnea,
cough,
and
fatigue,
it
was
observed
a
high
incidence
thromboembolic
events
potentially
evolving
towards
acute
respiratory
distress
syndrome
(ARDS)
COVID-19-associated-coagulopathy
(CAC).
The
hypercoagulation
state
is
based
on
an
interaction
between
thrombosis
inflammation.
so-called
CAC
represents
key
aspect
in
genesis
organ
damage
from
SARS-CoV-2.
prothrombotic
status
can
be
explained
by
increase
coagulation
levels
D-dimer,
lymphocytes,
fibrinogen,
interleukin
6
(IL-6),
prothrombin
time.
Several
mechanisms
have
been
hypothesized
to
explain
this
hypercoagulable
process
such
as
inflammatory
cytokine
storm,
platelet
activation,
endothelial
dysfunction,
stasis
for
long
purpose
narrative
review
provide
overview
current
knowledge
pathogenic
coagulopathy
that
may
characterize
infection
inform
new
areas
research.
New
vascular
therapeutic
strategies
are
also
reviewed.