Scientific Reports,
Journal Year:
2022,
Volume and Issue:
12(1)
Published: Nov. 27, 2022
Abstract
Longitudinal
studies
have
revealed
large
interindividual
differences
in
antibody
responses
induced
by
SARS-CoV-2
mRNA
vaccines.
Thus,
we
performed
a
comprehensive
analysis
of
adaptive
immune
three
doses
the
BNT162b2
The
spike-specific
CD4
+
T
cells,
CD8
cells
and
serum
IgG,
neutralization
capacities
two
vaccines
declined
6
months
later.
3
rd
dose
increased
spike
IgG
neutralizing
against
wild-type
Omicron
spikes
to
higher
levels
than
2
nd
dose,
this
was
supported
memory
B
cell
responses,
which
gradually
after
were
further
enhanced
dose.
moderately
frequencies
but
remained
unchanged.
reactive
1.3-fold
fewer
those
spike.
early
responsiveness
T,
circulating
follicular
helper
peripheral
correlated
with
booster
vaccination,
also
associated
responses.
These
findings
highlight
importance
evaluating
cellular
optimize
future
vaccine
strategies.
Scientific Reports,
Journal Year:
2024,
Volume and Issue:
14(1)
Published: May 24, 2024
The
immune
effector
mechanisms
involved
in
protecting
against
severe
COVID-19
infection
elderly
nursing
home
residents
following
vaccination
or
natural
are
not
well
understood.
Here,
we
measured
SARS-CoV-2
Spike
(S)-directed
functional
antibody
responses,
including
neutralizing
antibodies
(NtAb)
and
Fc-mediated
NK
cell
activity
(degranulation
IFNγ
production),
the
Wuhan-Hu-1,
BA.4/5
(for
NtAb),
Omicron
XBB.1.5
variants
(n
=
39;
median
age,
91
years)
before
a
third
(pre-
post-3D)
fourth
post-4D)
mRNA
vaccine
dose.
Both
3D
4D
boosted
NtAb
levels
both
(sub)variants.
Likewise,
increased
ability
of
sera
to
trigger
LAMP1-
IFNγ-producing
cells,
particular
XBB.1.5.
In
contrast
titres,
frequencies
cells
activated
by
binding
Wuhan-Hu-1
S
were
comparable
at
all
testing
times.
Stronger
responses
observed
vaccine-experienced
participants
compared
vaccine-naïve
some
These
findings
can
contribute
identifying
reliable
correlate
protection
inform
future
strategies
this
population
group.
A
phase
1-2,
prospective,
multicenter,
randomized,
open-label
clinical
trial
(Code
RPCEC00000382,
https://rpcec.sld.cu/trials/RPCEC00000382-En/),
with
parallel
groups,
involving
1161
participants
was
designed
to
assess
safety
and
immunogenicity
of
two
Cuban
COVID-19
vaccines
(Mambisa
Abdala)
in
boosting
immunity
convalescent
adults
after
receiving
one
dose
either
vaccine.
The
main
outcome
severe
vaccination
adverse
events
occurring
<5%
vaccinees.
Main
success
endpoints
were
≥4-fold
anti-RBD
IgG
seroconversion
or
≥20%
increase
ACE2-RBD
inhibitory
antibodies
>55%
vaccinees
Phase
1
>70%
2.
Neutralizing
antibody
titers
against
SARS-CoV-2
variants
evaluated.
Both
safe;
no
deaths
occurred.
Mild
intensity
the
most
frequent
(>73%);
headache
predominated
for
both
vaccines.
responders
83.3%
(p
=
0.0018)
Abdala.
Mambisa
showed
similar
results.
2
88.6%
Abdala
<0.0001)
74.2%
0.0412).
In
phases,
titers,
inhibition
percentages
neutralizing
increased
significantly
booster
dose.
safe
their
surpassed
study
endpoints.
Vaccines,
Journal Year:
2024,
Volume and Issue:
12(7), P. 781 - 781
Published: July 16, 2024
Background:
Several
COVID-19
vaccines
were
developed
and
approved
in
China.
Of
these,
the
BIBB-CorV
CoronaVac
inactivated
whole-virion
widely
distributed
China
developing
countries.
However,
performance
of
two
real
world
has
not
been
summarized.
Methods:
A
living
systematic
review
based
on
findings
from
ongoing
post-licensure
studies
was
conducted,
applying
standardized
algorithms.
Articles
published
between
1
May
2020
31
2022
English
Chinese
searched
for
Medline,
Embase,
WanFang
Data,
medRxiv,
bioRxiv,
arXiv,
SSRN,
Research
Square,
using
SARS-CoV-2,
COVID-19,
vaccine
as
MeSH
terms.
Studies
with
estimates
safety,
immunogenicity,
effectiveness
receiving
or
that
met
predefined
screening
criteria
underwent
a
full-text
review.
The
Joanna
Briggs
Institute’s
Critical
Appraisal
Checklist
Cochrane
risk
bias
used
assessment
quality.
random-effects
meta-regression
model
applied
to
identify
potential
impact
factors
vaccines’
effectiveness.
Results:
In
total,
32578
articles
identified,
770
Eventually,
213
included.
pooled
occurrence
solicited
unsolicited
adverse
events
after
any
dose
either
varied
10%
40%.
top
five
commonly
reported
rare
immunization
stress-related
responses
(211
cases,
50.0%),
cutaneous
(43
10.2%),
acute
neurological
syndrome
(39
9.2%),
anaphylaxis
(17
4.0%),
stroke
(16
3.8%).
majority
(83.3%)
recovered
relieved
within
several
days.
peak
neutralization
titers
against
ancestral
strain
found
month
completion
primary
series
vaccine,
GMT
(geometric
mean
titer)
43.7
(95%
CI:
23.2–82.4),
followed
by
dramatic
decrease
3
months.
At
Month
12,
4.1
3.8–4.4).
Homologous
boosting
could
restore
humoral
immunity,
while
heterologous
elicited
around
sixfold
higher
comparison
homologous
boosting.
death
severe
disease
85%
both
shortly
series.
protection
did
decline,
decreased
~75%.
Conclusions:
Both
BIBP-CorV
are
safe.
Sustained
determined
12
months
series,
although
slightly
over
time.
booster
strengthen
waning
effectiveness;
however,
duration
incremental
additional
benefit
provided
need
be
studied.
Vaccines,
Journal Year:
2024,
Volume and Issue:
12(9), P. 1001 - 1001
Published: Sept. 1, 2024
A
phase
1–2,
prospective,
multicenter,
randomized,
open-label
clinical
trial
(Code
RPCEC00000382),
with
parallel
groups,
involving
1161
participants,
was
designed
to
assess
the
safety
and
immunogenicity
of
two
Cuban
COVID-19
vaccines
(Mambisa
Abdala)
in
boosting
immunity
convalescent
adults
after
receiving
one
dose
either
vaccine.
The
main
outcome
severe
vaccination
adverse
events
occurring
<5%
vaccinees.
Main
success
endpoints
were
a
≥4-fold
anti-RBD
IgG
seroconversion
or
≥20%
increase
ACE2-RBD
inhibitory
antibodies
>55%
vaccinees
Phase
1
>70%
2.
Neutralizing
antibody
titers
against
SARS-CoV-2
variants
evaluated.
Both
safe—no
deaths
occurred.
Mild
intensity
most
frequent
(>73%);
headaches
predominated
for
both
vaccines.
responders
83.3%
(p
=
0.0018)
Abdala.
Mambisa
showed
similar
results.
2
88.6%
Abdala
<
0.0001)
74.2%
0.0412).
In
phases,
titers,
inhibition
percentages
neutralizing
increased
significantly
booster
dose.
safe
their
surpassed
study
endpoints.
Scientific Reports,
Journal Year:
2022,
Volume and Issue:
12(1)
Published: Nov. 27, 2022
Abstract
Longitudinal
studies
have
revealed
large
interindividual
differences
in
antibody
responses
induced
by
SARS-CoV-2
mRNA
vaccines.
Thus,
we
performed
a
comprehensive
analysis
of
adaptive
immune
three
doses
the
BNT162b2
The
spike-specific
CD4
+
T
cells,
CD8
cells
and
serum
IgG,
neutralization
capacities
two
vaccines
declined
6
months
later.
3
rd
dose
increased
spike
IgG
neutralizing
against
wild-type
Omicron
spikes
to
higher
levels
than
2
nd
dose,
this
was
supported
memory
B
cell
responses,
which
gradually
after
were
further
enhanced
dose.
moderately
frequencies
but
remained
unchanged.
reactive
1.3-fold
fewer
those
spike.
early
responsiveness
T,
circulating
follicular
helper
peripheral
correlated
with
booster
vaccination,
also
associated
responses.
These
findings
highlight
importance
evaluating
cellular
optimize
future
vaccine
strategies.