Vaccines,
Journal Year:
2024,
Volume and Issue:
12(12), P. 1401 - 1401
Published: Dec. 12, 2024
The
research
conducted
in
this
preclinical
study
assesses
QazCovid-live,
a
live
attenuated
COVID-19
vaccine
created
Kazakhstan,
by
conducting
evaluations
of
safety,
immunogenicity,
and
allergenicity
various
animal
models,
including
mice,
rats,
hamsters,
guinea
pigs.
vaccine,
developed
attenuating
SARS-CoV-2
via
numerous
Vero
cell
passages,
had
no
significant
adverse
effects
acute
subacute
toxicity
assessments,
even
at
elevated
dosages.
Allergenicity
testing
indicated
the
absence
both
immediate
delayed
hypersensitivity
reactions.
Immunogenicity
revealed
strong
virus-neutralizing
antibody
responses,
especially
following
intranasal
intratracheal
delivery.
Studies
on
reversibility
transmission
further
validated
vaccine’s
stability
non-pathogenicity.
data
indicate
that
QazCovid-live
is
safe,
immunogenic,
prepared
for
clinical
trials,
presenting
potential
strategy
prevention.
iScience,
Journal Year:
2024,
Volume and Issue:
27(9), P. 110174 - 110174
Published: June 5, 2024
Antibodies
represent
a
primary
mediator
of
protection
against
respiratory
viruses.
Serum
neutralizing
antibodies
(NAbs)
are
often
considered
correlate
protection.
However,
detailed
antibody
profiles
including
characterization
functions
in
different
anatomic
compartments
poorly
understood.
Here
we
show
that
correlates
severe
acute
syndrome
coronavirus
2
(SARS-CoV-2)
challenge
systemic
versus
mucosal
rhesus
macaques.
In
serum,
NAbs
were
the
strongest
and
linked
to
spike-specific
binding
other
extra-NAb
create
larger
protective
network.
bronchiolar
lavage
(BAL),
antibody-dependent
cellular
phagocytosis
(ADCP)
proved
rather
than
NAbs.
Within
BAL,
ADCP
was
immunoglobulin
(Ig)G,
IgA/secretory
IgA,
Fcγ-receptor
antibodies.
Our
results
support
model
which
with
mediate
at
sites.
Vaccines,
Journal Year:
2024,
Volume and Issue:
12(10), P. 1126 - 1126
Published: Sept. 30, 2024
The
innate
and
adaptive
immune
systems
collaborate
to
detect
SARS-CoV-2
infection,
minimize
the
viral
spread,
kill
infected
cells,
ultimately
leading
resolution
of
infection.
system
develops
a
memory
previous
encounters
with
virus,
providing
enhanced
responses
when
rechallenged
by
same
pathogen.
Such
immunological
is
basis
vaccine
function.
Here,
we
review
current
knowledge
on
response
infection
vaccination,
focusing
pivotal
role
T
cells
in
establishing
protective
immunity
against
virus.
After
an
overview
describe
main
features
SARS-CoV-2-specific
CD4
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: March 1, 2024
Abstract
Antibodies
represent
a
primary
mediator
of
protection
against
respiratory
viruses
such
as
SARS-CoV-2.
Serum
neutralizing
antibodies
(NAbs)
are
often
considered
correlate
protection.
However,
detailed
antibody
profiles
including
characterization
functions
in
different
anatomic
compartments
not
well
understood.
Here
we
show
that
correlates
SARS-CoV-2
challenge
systemic
versus
mucosal
rhesus
macaques.
In
serum,
were
the
strongest
and
linked
to
Spike-specific
binding
other
extra-neutralizing
create
larger
protective
network.
contrast,
bronchiolar
lavage
(BAL),
antibody-dependent
cellular
phagocytosis
(ADCP)
proved
rather
than
NAbs.
Within
BAL,
ADCP
was
IgG,
IgA/secretory
IgA,
Fcγ-receptor
antibodies.
Our
results
support
model
which
with
mediate
at
sites.
The
correlation
Fc
functional
responses
BAL
suggests
these
may
be
critical
for
Omicron
mucosa.
Vaccines,
Journal Year:
2024,
Volume and Issue:
12(10), P. 1089 - 1089
Published: Sept. 24, 2024
Correlates
of
Protection
(CoP)
are
biomarkers
above
a
defined
threshold
that
can
replace
clinical
outcomes
as
primary
endpoints,
predicting
vaccine
effectiveness
to
support
the
approval
new
vaccines
or
follow
up
studies.
In
context
COVID-19
vaccination,
CoPs
help
address
challenges
such
demonstrating
in
special
populations,
against
emerging
SARS-CoV-2
variants
determining
durability
vaccine-elicited
immunity.
While
anti-spike
IgG
titres
and
viral
neutralising
capacity
have
been
characterised
for
contribution
other
components
humoral
immune
response
immediate
long-term
protective
immunity
is
less
well
characterised.
This
review
examines
evidence
supporting
use
trials,
how
they
be
used
define
It
also
highlights
alternative
biomarkers,
including
Fc
effector
function,
mucosal
immunity,
generation
long-lived
plasma
memory
B
cells
discuss
these
applied
studies
tools
available
study
them.
Vaccines,
Journal Year:
2024,
Volume and Issue:
12(10), P. 1191 - 1191
Published: Oct. 18, 2024
Background:
Long-lived,
re-activatable
immunity
to
SARS-CoV-2
and
its
emerging
variants
will
rely
on
T
cells
recognizing
conserved
regions
of
viral
proteins
across
strains.
Heterologous
prime–boost
regimens
can
elicit
elevated
levels
circulating
CD8+
that
provide
a
reservoir
first
responders
upon
infection.
Although
most
vaccines
are
currently
delivered
intramuscularly
(IM),
the
initial
site
infection
is
nasal
cavity.
Methods:
Here,
we
tested
hypothesis
heterologous
prime
boost
vaccine
regimen
intranasally
(IN)
generate
improved
immune
responses
locally
at
virus
compared
intramuscular
vaccine/booster
regimens.
Results:
In
transgenic
human
ACE2
murine
model,
both
Spike-expressing
single-cycle
adenovirus
(SC-Ad)
an
IFNß
safety-enhanced
replication-competent
Vesicular
Stomatitis
Virus
(VSV)
platform
generated
anti-Spike
antibody
T-cell
diminished
with
age.
SC-Ad-Spike
boosted
VSV-Spike-mIFNß,
alone
induced
maximal
IgG,
IgA,
responses.
Conclusions:
There
were
significant
differences
in
spleens
lungs,
intranasal
was
significantly
superior
generating
sentinel
effectors
encounter
lungs.
These
data
show
serious
consideration
should
be
given
boosting
anti-SARS-CoV-2
vaccines.
Vaccines,
Journal Year:
2024,
Volume and Issue:
12(12), P. 1401 - 1401
Published: Dec. 12, 2024
The
research
conducted
in
this
preclinical
study
assesses
QazCovid-live,
a
live
attenuated
COVID-19
vaccine
created
Kazakhstan,
by
conducting
evaluations
of
safety,
immunogenicity,
and
allergenicity
various
animal
models,
including
mice,
rats,
hamsters,
guinea
pigs.
vaccine,
developed
attenuating
SARS-CoV-2
via
numerous
Vero
cell
passages,
had
no
significant
adverse
effects
acute
subacute
toxicity
assessments,
even
at
elevated
dosages.
Allergenicity
testing
indicated
the
absence
both
immediate
delayed
hypersensitivity
reactions.
Immunogenicity
revealed
strong
virus-neutralizing
antibody
responses,
especially
following
intranasal
intratracheal
delivery.
Studies
on
reversibility
transmission
further
validated
vaccine’s
stability
non-pathogenicity.
data
indicate
that
QazCovid-live
is
safe,
immunogenic,
prepared
for
clinical
trials,
presenting
potential
strategy
prevention.