Biomarkers in Medicine,
Год журнала:
2024,
Номер
18(10-12), С. 555 - 565
Опубликована: Июнь 17, 2024
Methods:
Demographic
characteristics,
clinical
and
laboratory
data,
thorax
computed
tomography
(CT)
images,
second-year
survival
status,
causes
of
death
were
analyzed.
Biomolecules,
Год журнала:
2023,
Номер
13(11), С. 1565 - 1565
Опубликована: Окт. 24, 2023
The
Coronavirus
disease-2019
(COVID-19),
caused
by
the
severe
acute
respiratory
syndrome
coronavirus-2
(SARS-CoV-2),
has
significantly
impacted
health
and
socioeconomic
status
of
humans
worldwide.
Pulmonary
infection
SARS-CoV-2
results
in
exorbitant
viral
replication
associated
onset
inflammatory
cytokine
storm
disease
pathology
various
internal
organs.
However,
etiopathogenesis
is
not
fully
understood.
Currently,
there
are
no
targeted
therapies
available
to
cure
COVID-19,
most
patients
treated
empirically
with
anti-inflammatory
and/or
anti-viral
drugs,
based
on
symptoms.
Although
several
types
vaccines
currently
implemented
control
COVID-19
prevent
dissemination,
emergence
new
variants
that
can
evade
vaccine-induced
protective
immunity
poses
challenges
current
vaccination
strategies
highlights
necessity
develop
better
improved
vaccines.
In
this
review,
we
summarize
elaborately
discuss
strategies,
focusing
those
use
worldwide
combat
or
stages
clinical
development
humans.
medRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2024,
Номер
unknown
Опубликована: Ноя. 13, 2024
ABSTRACT
Background
Pemivibart
received
emergency-use
authorization
for
prevention
of
symptomatic
COVID-19
in
moderate-to-severe
immunocompromised
individuals
based
on
immunobridging
analysis
the
phase
3
CANOPY
trial.
We
report
an
interim
safety
and
efficacy
pemivibart
with
(cohort
A)
or
without
B)
significant
immunocompromise
over
a
contemporary
variant
landscape.
Methods
Eligible
participants
(aged
≥18
years;
SARS-CoV-2-negative)
2
intravenous
4500-mg
infusions
blinded
placebo
(2:1,
cohort
90
days
apart.
Safety
was
primary
endpoint.
Composite
incidence
reverse
transcription-polymerase
chain
reaction
(RT-PCR)-confirmed
COVID-19,
hospitalization,
all-cause
mortality
evaluated
through
month
6
12
B).
Results
In
September-November
2023,
306
A;
317
162
B.
The
most
common
study
drug-related
adverse
event
infusion-related
reactions
A:
11/306
[3.6%];
B:
7/317
[2.2%,
pemivibart]
0/162
[placebo]).
Four
623
(0.6%)
who
experienced
anaphylactic
(2
non-serious;
serious)
within
24
hours
dosing.
A,
composite
endpoint
(day
180)
11/298
(3.7%;
deaths
[suicide
unknown
cause])
first
full
dose
pemivibart.
B,
6/317
(1.9%)
group
19/160
(11.9%)
group,
representing
84.1%
standardized
relative
risk
reduction
(RRR)
(95%
CI,
60.9-93.5;
nominal
P
<.0001)
Through
12,
15/317
(4.7%;
1
death
[cardiac
failure])
29/160
(18.1%)
met
clinical
endpoint,
respectively
demonstrating
73.9%
RRR
52.8-85.6;
<.0001).
Conclusions
provided
pre-exposure
prophylactic
against
well-tolerated
by
immunocompromise.
Anaphylaxis
important
risk.
Clinical
Trials
Registration
NCT06039449
Key
points
Pre-exposure
administration
doses
approximately
apart
generally
protection
months
Antibody Therapeutics,
Год журнала:
2023,
Номер
6(4), С. 277 - 297
Опубликована: Окт. 1, 2023
Abstract
Background
Due
to
COVID-19,
pandemic
preparedness
emerges
as
a
key
imperative,
necessitating
new
approaches
accelerate
development
of
reagents
against
infectious
pathogens.
Methods
Here,
we
developed
an
integrated
approach
combining
synthetic,
computational
and
structural
methods
with
in
vitro
antibody
selection
vivo
immunization
design,
produce
validate
nature-inspired
nanoparticle-based
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2).
Results
Our
resulted
two
innovations:
(i)
thermostable
nasal
vaccine
called
ADDoCoV,
displaying
multiple
copies
SARS-CoV-2
receptor
binding
motif
derived
epitope
(ii)
multivalent
nanoparticle
superbinder,
Gigabody,
including
immune-evasive
variants
concern
(VOCs).
In
generated
neutralizing
nanobodies
electron
cryo-microscopy
established
authenticity
accessibility
epitopes
displayed
by
ADDoCoV.
Gigabody
comprising
multimerized
prevented
virion
attachment
picomolar
EC50.
Vaccinating
mice
antibodies
cross-reacting
VOCs
Delta
Omicron.
Conclusion
study
elucidates
Adenovirus-derived
dodecamer
(ADDomer)-based
nanoparticles
for
use
active
passive
provides
blueprint
crafting
combat
viral
infections.
American Journal of Forensic Medicine & Pathology,
Год журнала:
2023,
Номер
44(3), С. 157 - 165
Опубликована: Май 26, 2023
Abstract
The
King
County
Medical
Examiner's
Office
in
Seattle,
Wash,
initiated
a
surveillance
project
with
dedicated
team
and
database
tracking
the
spread
of
severe
acute
respiratory
syndrome
coronavirus
2,
deaths
due
to
disease
2019
(COVID-19),
occurring
within
28
days
COVID-19
vaccination.
From
January
2020
through
July
2022,
results
13,801
nasal/nasopharyngeal
swabs
from
7606
decedents
tested
for
virus
were
assembled
database.
Generally,
2
samples
collected
separately
by
different
laboratories.
Positive
rates
increased
5.7%
14.3%
2022.
Of
744
positive
virus,
autopsies
performed
on
418
(56%);
these,
106
(25%)
died
as
either
primary
or
contributing
cause.
Comparison
autopsy
findings
those
dying
but
other
causes
demonstrated
risk
preexisting
conditions.
1035
reported
vaccination,
thrombotic
complications
myocarditis
no
higher
than
decedents.
This
study
provides
evidence
value
public
health
an
adequately
resourced
medical
examiner
office
viral
community,
understanding
mortality,
assessing
vaccine
safety.
Current Topics in Medicinal Chemistry,
Год журнала:
2023,
Номер
23(26), С. 2436 - 2451
Опубликована: Авг. 30, 2023
The
COVID-19
pandemic
was
the
most
significant
public
healthcare
crisis
worldwide.
It
estimated
that
80%
of
infected
patients
with
have
not
fully
recovered
and
developed
one
or
more
long-term
symptoms,
referred
to
as
post-acute
sequelae
(PASC).
Seeking
a
treatment
strategy
for
PASC
has
become
concerning
topic
since
can
cause
irreversible
multiple
organ
damage
severely
compromise
quality
life.
is
indicated
may
be
closely
related
lung
injury-induced
hypoxia,
excessive
immune
response,
cytokine
storm,
gut
bacteria
imbalance,
endothelial
dysfunction.
Also,
research
angiotensin-converting
enzyme
2
(ACE2)
receptor,
transient
receptor
potential
ankyrin
1
vanillin
(TRPA1/V1),
nuclear
factor
erythroid
2-related
(Nrf2)
considered
targets
treat
PASC.
There
currently
still
no
proven
medication
due
its
complexity.
Many
clinical
practices
studies
shown
natural
products
great
in
preventing
treating
Therefore,
we
intended
provide
comprehensive
review
current
literature
on
role
ingredients
management.
Meanwhile,
this
provided
meaningful
insight
further
study
improve
application.
Viruses,
Год журнала:
2024,
Номер
16(3), С. 391 - 391
Опубликована: Март 1, 2024
The
surface
spike
(S)
glycoprotein
mediates
cell
entry
of
SARS-CoV-2
into
the
host
through
fusion
at
plasma
membrane
or
endocytosis.
Omicron
lineages/sublineages
have
acquired
extensive
mutations
in
S
to
gain
transmissibility
advantages
and
altered
antigenicity.
fusogenicity,
antigenicity,
evasion
subvariants
been
extensively
investigated
unprecedented
speed
align
with
mutation
rate
S.
Cells
that
overexpress
receptors/cofactors
are
mostly
used
as
hosts
amplify
infection
sensitivity
tested
variants.
However,
systematic
comparisons
most
prior
dominant
using
human
lung
epithelium
cells
yet
be
well-studied.
Here,
bronchial
BEAS-2B
host,
we
compared
single-round
virus-to-cell
cell-to-cell
BA.1,
BA.5,
BQ.1.1,
CH.1.1,
XBB.1.5,
XBB.1.16
based
upon
split
NanoLuc
readout
assays
S-pseudotyped
lentivirus
system.
Virus-to-cell
variants
exhibited
cell-type
dependence.
parental
BA.1
required
more
time
develop
full
HEK293T-ACE2-TMPRSS2
than
cells.
Compared
unchanged
P681,
S-cleavage
constructs
P681H/R
did
not
any
noticeable
entry.
its
descendants
entered
efficiently
D614G,
it
was
slightly
less
comparable
Delta.
Serine
protease-pretreated
enhanced
a
dose-dependent
manner,
suggesting
persists
productive
route.
Spike-mediated
total
S1/S2
processing
were
similar.
Our
results
indicate
no
obvious
recent
over
preceding
since
Delta,
thus
supporting
immune
conferred
by
antigenicity
shifts
due
sequences
probably
primary
viral
fitness
driver.
Since
the
reports
of
first
cases
COVID-19,
in
less
than
5
years
a
huge
number
documents
regarding
that
disease
and
coronavirus
(SARS-CoV-2),
responsible
for
infection,
have
been
published.
The
tremendous
scientific
covers
many
topics
on
different
issues
directly
related
to
COVID-19/SARS-CoV-2.
It
includes
studies
about
efficacy
vaccines
prevent
disease.
However,
only
comparatively
low
nonclinical
-conducted
experimental
animals-
focused
potential
adverse/toxic
effects
COVID-19
vaccines.
present
review
was
aimed
at
revising
literature
laboratory
animals
toxic/adverse
In
addition,
investigations
reported
those
specific
toxicology
journals
with
highest
impact
factors
examined
one
by
one.
results
indicate
most
nonclinical/experimental
and/or
candidates
showed
-in
general
terms-
good
safety
profile.
Only
some
animal
were
certain
adverse
found.
rather
surprising
result
has
limited
available
(in
databases
PubMed
Scopus)
performed
companies
largest
manufacturers
mRNA
world
[https://www.google.com/search?sca_esv=ba085665fbb45bd4&sca_upv=1&q=Who+is+the+largest+manufacturer+of+vaccines+in+the+world%3F&sa=X&sqi=2&ved=2ahUKEwj6nMbAi-qGAxVLaqQEHTPwDcIQzmd6BAgZEAY].
Why
these
-assuming,
course,
they
conducted-
not
published
journals,
allowing
judgment
international
community,
including
toxicologists?
Biomarkers in Medicine,
Год журнала:
2024,
Номер
18(10-12), С. 555 - 565
Опубликована: Июнь 17, 2024
Methods:
Demographic
characteristics,
clinical
and
laboratory
data,
thorax
computed
tomography
(CT)
images,
second-year
survival
status,
causes
of
death
were
analyzed.