Science Immunology,
Journal Year:
2021,
Volume and Issue:
6(66)
Published: Oct. 14, 2021
SARS-CoV-2
has
caused
a
global
pandemic
that
infected
more
than
250
million
people
worldwide.
Although
several
vaccine
candidates
have
received
emergency
use
authorization,
there
is
still
limited
knowledge
on
how
dosing
affects
immune
responses.
We
performed
mechanistic
studies
in
mice
to
understand
the
priming
dose
of
an
adenovirus-based
long-term
immunity
SARS-CoV-2.
first
primed
C57BL/6
with
adenovirus
serotype
5
encoding
spike
protein,
similar
used
CanSino
and
Sputnik
V
vaccines.
The
prime
was
administered
at
either
standard
or
1000-fold
lower
dose,
followed
by
boost
4
weeks
later.
Initially,
low
induced
responses
relative
prime.
However,
elicited
were
qualitatively
superior
and,
upon
boosting,
exhibited
substantially
potent
recall
functional
capacity.
also
report
effects
simian
immunodeficiency
virus
(SIV)
vaccine.
These
findings
show
unexpected
advantage
fractionating
doses,
warranting
reevaluation
trial
protocols
for
other
pathogens.
npj Vaccines,
Journal Year:
2023,
Volume and Issue:
8(1)
Published: March 16, 2023
Abstract
Emerging
SARS-CoV-2
Omicron
subvariants
continue
to
disrupt
COVID-19
vaccine
efficacy
through
multiple
immune
mechanisms
including
neutralizing
antibody
evasion.
We
developed
COH04S1,
a
synthetic
modified
vaccinia
Ankara
vector
that
co-expresses
Wuhan-Hu-1-based
spike
and
nucleocapsid
antigens.
COH04S1
demonstrated
against
ancestral
virus
Beta
Delta
variants
in
animal
models
was
safe
immunogenic
Phase
1
clinical
trial.
Here,
we
report
of
analogous
BA.1-
Beta-specific
vaccines
protect
Syrian
hamsters
from
subvariants.
Despite
eliciting
strain-specific
responses,
all
three
weight
loss,
lower
respiratory
tract
infection,
lung
pathology
following
challenge
with
BA.1
or
BA.2.12.1.
While
the
BA.1-specifc
affords
consistently
improved
compared
homologous
BA.1,
confer
similar
protection
heterologous
These
results
demonstrate
variant-specific
derivatives
cross-protective
immunity
Frontiers in Cellular and Infection Microbiology,
Journal Year:
2024,
Volume and Issue:
14
Published: May 23, 2024
Corona
Virus
Disease
2019
(COVID-19)
is
a
highly
prevalent
and
potent
infectious
disease
caused
by
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2).
Until
now,
the
world
still
endeavoring
to
develop
new
ways
diagnose
treat
COVID-19.
At
present,
clinical
prevention
treatment
of
COVID-19
mainly
targets
spike
protein
on
surface
SRAS-CoV-2.
However,
with
continuous
emergence
SARS-CoV-2
Variants
concern
(VOC),
targeting
therapy
shows
high
degree
limitation.
The
Nucleocapsid
Protein
(N
protein)
conserved
in
virus
evolution
involved
key
process
viral
infection
assembly.
It
most
expressed
structural
after
humans
has
immunogenicity.
Therefore,
N
as
factor
replication
basic
research
application
great
potential
value.
This
article
reviews
progress
structure
biological
function
protein,
diagnosis
drug
order
promote
researchers’
further
understanding
lay
theoretical
foundation
for
possible
outbreak
sudden
diseases
future.
medRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2021,
Volume and Issue:
unknown
Published: Aug. 9, 2021
Many
people
experiencing
long
COVID
syndrome,
or
post-acute
sequelae
of
SARS-CoV-2
infection
(PASC),
suffer
from
debilitating
neurologic
symptoms
(Neuro-PASC).
However,
whether
virus-specific
adaptive
immunity
is
affected
in
Neuro-PASC
patients
remains
poorly
understood.
We
report
that
exhibit
distinct
immunological
signatures
composed
elevated
humoral
and
cellular
responses
toward
Nucleocapsid
protein
at
an
average
6
months
post-infection
compared
to
healthy
convalescents.
also
had
enhanced
production
IL-6
diminished
activation
CD8
+
T
cells.
Furthermore,
the
severity
cognitive
deficits
quality
life
disturbances
were
associated
with
a
reduced
diversity
effector
molecule
expression
cells
but
IFN-γ
C-terminal
domain
protein.
Proteomics
analysis
showed
plasma
immunoregulatory
proteins
pro-inflammatory
antiviral
response
convalescents,
which
correlated
worse
neurocognitive
dysfunction.
These
data
provide
new
insight
into
pathogenesis
syndrome
framework
for
rational
design
predictive
biomarkers
therapeutic
interventions.Adaptive
altered
manifestations
COVID.
Science Immunology,
Journal Year:
2021,
Volume and Issue:
6(66)
Published: Oct. 14, 2021
SARS-CoV-2
has
caused
a
global
pandemic
that
infected
more
than
250
million
people
worldwide.
Although
several
vaccine
candidates
have
received
emergency
use
authorization,
there
is
still
limited
knowledge
on
how
dosing
affects
immune
responses.
We
performed
mechanistic
studies
in
mice
to
understand
the
priming
dose
of
an
adenovirus-based
long-term
immunity
SARS-CoV-2.
first
primed
C57BL/6
with
adenovirus
serotype
5
encoding
spike
protein,
similar
used
CanSino
and
Sputnik
V
vaccines.
The
prime
was
administered
at
either
standard
or
1000-fold
lower
dose,
followed
by
boost
4
weeks
later.
Initially,
low
induced
responses
relative
prime.
However,
elicited
were
qualitatively
superior
and,
upon
boosting,
exhibited
substantially
potent
recall
functional
capacity.
also
report
effects
simian
immunodeficiency
virus
(SIV)
vaccine.
These
findings
show
unexpected
advantage
fractionating
doses,
warranting
reevaluation
trial
protocols
for
other
pathogens.