Frontiers in Immunology,
Journal Year:
2023,
Volume and Issue:
14
Published: Nov. 20, 2023
A
real-world
population-based
longitudinal
study,
aimed
at
determining
the
magnitude
and
duration
of
immunity
induced
by
different
types
vaccines
against
COVID-19,
started
in
2021
enrolling
a
cohort
2,497
individuals
time
their
first
vaccination.
The
study
included
both
healthy
adults
aged
≤65
years
elderly
subjects
>65
with
two
or
more
co-morbidities.
Here,
patterns
anti-SARS-CoV-2
humoral
cell-mediated
specific
immune
response,
assessed
on
1,182
remaining
subjects,
6
(T6)
12
months
(T12)
after
vaccine
dose,
are
described.
At
T12
median
anti-Spike
IgG
antibody
levels
were
increased
compared
to
T6.
determinants
receipt
third
dose
between
T6
being
positive
for
anti-Nucleocapside
T12,
marker
recent
infection,
while
age
had
no
significant
effect.
capacity
sera
neutralize
vitro
ancestral
B
strain
Omicron
BA.5
variant
was
subgroup
vaccinated
subjects.
correlation
anti-S
neutralizing
identified
higher
evident
frail
those
who
T12.
Remarkably,
one
from
negative
older
unable
strain.
Finally,
evaluation
T-cell
mediated
showed
that
most
analysed
independently
comorbidity,
displayed
Spike-specific
responses
high
degree
polyfunctionality,
especially
CD8
compartment.
In
conclusion,
circulating
antibodies
SARS-CoV-2
Spike
protein
primary
vaccination,
which
as
enhancing
effect
could
be
attributable
administration
but
also
occurrence
breakthrough
infection.
Older
individuals,
negative,
an
impaired
responses,
able
sustain
maintain
ability
fight
present
younger
assayed
New England Journal of Medicine,
Journal Year:
2023,
Volume and Issue:
389(17), P. 1590 - 1600
Published: Oct. 25, 2023
Passive
immunization
with
plasma
collected
from
convalescent
patients
has
been
regularly
used
to
treat
coronavirus
disease
2019
(Covid-19).
Minimal
data
are
available
regarding
the
use
of
in
Covid-19-induced
acute
respiratory
distress
syndrome
(ARDS).
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: Feb. 18, 2025
Since
early
2020,
several
SARS-CoV-2
variants
of
concern
(VOCs)
continue
to
emerge,
evading
waning
antibody
mediated
immunity
produced
by
the
current
Spike-alone
based
COVID-19
vaccines.
This
caused
a
prolonged
and
persistent
pandemic
that
is
going
enter
its
fifth
year.
Thus,
need
remains
for
innovative
next
generation
vaccines
would
incorporate
protective
Spike-derived
B-cell
epitopes
resist
immune
evasion.
Towards
goal,
in
this
study
we
(i)
Screened
sequences
Spike
among
many
VOCs
identified
conserved
non-conserved
linear
epitopes;
(ii)
Compared
titers
neutralization
antibodies
specific
these
from
serum
symptomatic
asymptomatic
patients
were
exposed
multiple
across
5-year
pandemic,
(iii)
efficacy
versus
against
most
pathogenic
Delta
variant
"humanized"
ACE-2/HLA
transgenic
mouse
model.
We
found
robust
epitope-specific
sera
patients.
In
contrast,
contained
weaker
responses
epitopes.
A
multi-epitope
vaccine
incorporated
epitopes,
but
not
significantly
protected
ACE2/HLA
mice
infection
like
symptoms
variant.
These
findings
underscore
importance
generating
severe
various
VOCs,
providing
valuable
insights
development
broad-spectrum
Coronavirus
capable
conferring
cross-variant
immunity.
Antibody
persistence
and
safety
up
to
12
months
of
heterologous
orally
administered
adenovirus
type-5
vector-based
COVID-19
vaccine
(Ad5-nCoV)
in
individuals
who
were
primed
with
two-dose
inactivated
SARS-CoV-2
(CoronaVac)
previously,
has
not
been
reported
yet.
This
randomized,
open-label,
single-centre
trial
included
Chinese
adults
have
received
CoronaVac
randomized
low-dose
or
high-dose
aerosolised
Ad5-nCoV
group,
group.
In
this
report,
we
mainly
evaluated
the
geometric
mean
titres
(GMTs)
neutralizing
antibodies
(NAbs)
against
live
wild-type
virus
omicron
BA.4/5
pseudovirus
at
after
booster
dose
incidence
serious
adverse
events
(SAEs)
till
month
12.
Of
419
participants,
all
analysis
120
(28.64%)
immunogenicity
analysis.
Serum
NAb
GMT
was
204.36
(95%
CI
152.91,
273.14)
group
171.38
121.27,
242.19)
12,
significantly
higher
than
(8.00
[95%
4.22,
15.17],
p
<
0.0001).
40.97
30.15,
55.67)
35.08
26.31,
46.77)
whereas
below
lower
limit
detection.
No
vaccine-related
SAEs
observed.
Orally
following
priming
a
good
profile
is
persistently
more
immunogenic
three-dose
within
dose.Trial
registration:
ClinicalTrials.gov
identifier:
NCT05043259..
Medicines,
Journal Year:
2023,
Volume and Issue:
10(4), P. 27 - 27
Published: April 20, 2023
Background:
The
rise
in
antibody
titers
against
the
novel
coronavirus
(SARS-CoV-2)
and
its
duration
are
considered
an
important
indicator
for
confirming
effect
of
a
COVID-19
vaccine,
self-paid
tests
titer
conducted
many
facilities
nationwide.
Methods:
relationship
between
number
days
after
second
third
dose
vaccines,
age,
was
determined
from
medical
records
general
internal
medicine
clinics
that
testing
SARS-CoV-2
using
Elecsys
Anti-SARS-CoV-2
S
(Roche
Diagnostics);
two
or
more
doses
vaccines
also
determined.
We
examined
cases
spontaneous
infection
with
vaccine.
Results:
Log-transformed
measured
within
1
month
vaccine
showed
negative
correlation
age
(p
<
0.05).
In
addition,
log-transformed
trend
=
0.055);
however,
there
were
no
significant
correlations
median
vaccination
18,300
U/mL,
than
10
times
1185
U/mL.
There
some
fourth
tens
thousands
U/ml
infection,
but
patients
still
received
further
booster
vaccinations
infection.
Conclusions:
did
not
attenuate
short
follow-up
period
one
month,
while
they
tended
to
vaccination.
It
is
people
Japan
even
though
already
had
U/mL
due
"hybrid
immunity"
following
clinical
significance
this
population
needs
be
thoroughly
investigated
should
prioritized
those
low
titers.
Frontiers in Immunology,
Journal Year:
2023,
Volume and Issue:
14
Published: May 2, 2023
Introduction
The
duration
and
timing
of
immunity
conferred
by
COVID-19
vaccination
in
sub-Saharan
Africa
are
crucial
for
guiding
pandemic
policy
interventions,
but
systematic
data
this
region
is
scarce.
This
study
investigated
the
antibody
response
after
AstraZeneca
convalescent
Ugandans.
Methods
We
recruited
86
participants
with
a
previous
rt-PCR-confirmed
mild
or
asymptomatic
infection
measured
prevalence
levels
spike-directed
IgG,
IgM,
IgA
antibodies
at
baseline,
14
28
days
first
dose
(priming),
second
(boosting),
six-
nine-months
post-priming.
also
nucleoprotein-directed
to
assess
breakthrough
infections.
Results
Within
two
weeks
priming,
substantially
increased
concentrations
(p
<
0.0001,
Wilcoxon
signed
rank
test),
97.0%
66%
vaccinated
individuals
possessing
S-IgG
S-IgA
before
administering
booster
dose.
S-IgM
changed
marginally
initial
barely
booster,
consistent
an
already
primed
immune
system.
However,
we
observed
rise
nucleoprotein
seroprevalence,
indicative
breakthroughs
six
months
vaccination.
Discussion
Our
results
suggest
that
vaccine
induces
robust
differential
response.
highlights
value
as
effective
method
inducing
previously
infected
importance
doses
maintain
protective
immunity.
Monitoring
anti-spike
IgG
when
assessing
vaccine-induced
responses
suggested
population;
will
underestimate
valuable
tool
fight
against
COVID-19.
Further
research
needed
determine
durability
potential
need
doses.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Feb. 15, 2024
ABSTRACT
The
first-generation
Spike-alone-based
COVID-19
vaccines
have
successfully
contributed
to
reducing
the
risk
of
hospitalization,
serious
illness,
and
death
caused
by
SARS-CoV-2
infections.
However,
waning
immunity
induced
these
failed
prevent
immune
escape
many
variants
concern
(VOCs)
that
emerged
from
2020
2024,
resulting
in
a
prolonged
pandemic.
We
hypothesize
next-generation
Coronavirus
(CoV)
vaccine
incorporating
highly
conserved
non-Spike
antigens
would
confer
stronger
broader
cross-protective
against
multiple
VOCs.
In
present
study,
we
identified
ten
are
8.7
million
strains,
twenty-one
VOCs,
SARS-CoV,
MERS-CoV,
Common
Cold
CoVs,
animal
CoVs.
Seven
10
were
preferentially
recognized
CD8
+
CD4
T-cells
unvaccinated
asymptomatic
patients,
irrespective
VOC
infection.
Three
out
seven
T
cell
belong
early
expressed
Replication
Transcription
Complex
(RTC)
region,
when
administered
golden
Syrian
hamsters,
combination
with
Spike,
as
nucleoside-modified
mRNA
encapsulated
lipid
nanoparticles
(LNP)
(i.e.,
combined
mRNA/LNP-based
pan-CoV
vaccine):
(
i
)
Induced
high
frequencies
lung-resident
antigen-specific
CXCR5
follicular
helper
(T
FH
cells,
GzmB
cytotoxic
cells
CYT
),
CD69
IFN-γ
TNFα
effector
EFF
);
ii
Reduced
viral
load
COVID-19-like
symptoms
various
including
pathogenic
B.1.617.2
Delta
variant
transmittable
heavily
Spike-mutated
XBB1.5
Omicron
sub-variant.
could
be
rapidly
adapted
for
clinical
use
emerging
mutated
IMPORTANCE
As
January
over
1500
individuals
United
States
alone
still
dying
each
week
despite
implementation
vaccines.
emergence
transmissible
(VOCs),
such
currently
circulating
BA.2.86
JN.1
sub-variants,
constantly
overrode
Here
report
next
generation
broad
spectrum
multi-antigen
consists
delivers
three
protein
together
Spike
B-cell
antigen.
Compared
side-by-side
clinically
proven
Spike-alone
vaccine,
vaccine-induced
higher
specific-neutralizing
antibodies.
This
was
associated
potent
cross-reactive
protection
sub-variants.
Our
findings
suggest
an
alternative
broad-spectrum
pan-Coronavirus
capable
disrupting
current
booster
paradigm;
outpacing
bivalent
variant-adapted
vaccines;
iii
ending
apparent
Frontiers in Cellular and Infection Microbiology,
Journal Year:
2024,
Volume and Issue:
14
Published: March 20, 2024
Background
The
aim
of
the
study
was
to
evaluate
humoral
and
cellular
immunity
after
SARS-CoV-2
infection
and/or
vaccination
according
type
vaccine,
number
doses
combination
vaccines.
Methods
Volunteer
subjects
were
sampled
between
September
2021
July
2022
in
Hospital
Clínico
San
Carlos,
Madrid
(Spain).
Participants
had
different
immunological
status
against
SARS-CoV-2:
vaccinated
unvaccinated,
with
or
without
previous
COVID-19
infection,
including
healthy
immunocompromised
individuals.
Determination
IgG
spike
protein
S1
subunit
receptor-binding
domain
(RBD)
performed
by
chemiluminescence
microparticle
immunoassay
(CMIA)
using
Architect
i10000sr
platform
(Abbott).
SARS-CoV-2-specific
T-cell
responses
assessed
quantification
interferon
gamma
release
QuantiFERON
assay
(Qiagen).
Results
A
total
181
samples
collected,
170
from
individuals
11
unvaccinated.
Among
participants,
41
aware
having
previously
been
infected
SARS-CoV-2.
Vaccinated
people
received
one
two
following
vaccines
ChAdOx1-S
(University
Oxford—AstraZeneca)
(AZ)
and/orBNT162b2
(Pfizer—BioNTech)(PZ).
Subjects
immunized
a
third-booster
dose
PZ
mRNA-1273
(Moderna—NIAID)(MD)
All
vaccinees
developed
positive
response
(>7.1
BAU/ml),
but
varied
depending
on
regimen.
Only
AZ/PZ
3
elicited
(median
concentration
IFN-
γ
>
0.3
IU/ml).
Regarding
two-dose
regimen,
induced
highest
immunity.
booster
mRNA
vaccine
resulted
increases
median
levels
IgG-Spike
antibodies
IFN-γ
as
compared
those
any
vaccine.
Humoral
significantly
higher
participants
infection.
Conclusion
Heterologous
(AZ/PZ)
strongest
among
regimens.
offered
depends
not
only
administered
also
prior
Previous
exposure
antigens
strongly
affect
Frontiers in Immunology,
Journal Year:
2023,
Volume and Issue:
14
Published: March 3, 2023
In
China,
the
long-term
immunogenicity
and
adverse
effects
of
inactivated
vaccines
produced
by
different
or
same
manufacturer
remain
unclear.
Therefore,
objective
this
study
was
to
evaluate
cellular
immune
responses
neutralizing
antibody
kinetics
homologous
heterologous
administrations
an
coronavirus
disease
2019
(COVID-19)
vaccine
240
days
after
second
vaccination.This
prospective,
multicenter,
observational,
longitudinal
involved
595
participants
with
a
negative
SARS-CoV-2
polymerase
chain
reaction
result
who
were
serologically
tested
followed
for
8
months
vaccination.
Neutralizing
antibodies,
interferon-gamma
(IFN-γ),
interleukin
(IL)-6,
CD4+
T-lymphocyte,
B-lymphocyte
counts
evaluated
in
serum
samples
stimulation
2
μg/mL
spike
protein
16
h
at
follow-up
intervals
months.Most
[582/595;
146
male
participants,
449
female
participants;
mean
age
35
(26-50
years)]
rapidly
developed
antibodies
two
doses
administered
3-weeks
apart.
The
positive
rate
peaked
97.7%
60-90
days,
decreased,
stabilized
82.9%
181-240
post-vaccination.
Lower
concentrations
correlated
older
age,
longer
duration
vaccination,
non-health
care
workers,
mixed-manufacturer
vaccinations,
less
than
40
between
whereas
lower
IFN-γ
levels
associated
blood
type
A,
workers.
A
higher
IL-6
level
medical
staff.
Adverse
reactions
mild
moderate
self-limited,
no
serious
events
reported.Two
Chinese
induced
robust
rapid
expression
responses.
Boosting
vaccination
is
considered
important,
as
reduced
susceptible
populations.
Vaccines,
Journal Year:
2023,
Volume and Issue:
11(4), P. 860 - 860
Published: April 17, 2023
Objective:
Severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
antibody
titers
level
and
duration
of
elevated
levels
are
considered
important
indicators
for
confirming
the
efficacy
disease
2019
(COVID-19)
vaccines.
The
objective
this
study
was
to
demonstrate
changes
in
after
second
third
doses
COVID-19
vaccine,
determine
cases
spontaneous
infection
with
SARS-CoV-2
vaccination.
Materials
Methods:
From
June
2021
February
2023,
IgG-type
were
measured
127
participants,
including
74
outpatients
53
members
staff,
at
Osaka
Dental
University
Hospital
(64
males
63
females,
mean
age
52.3
±
19.0
years).
Results:
Consistent
previous
reports,
titer
decreased
time,
not
only
dose
but
also
vaccine
if
there
no
infection.
We
confirmed
that
booster
vaccination
effective
increasing
titer.
A
total
21
natural
infections
observed
administering
two
or
more
vaccine.
Thirteen
these
patients
had
post-infection
exceeding
40,000
AU/mL,
some
continued
maintain
tens
thousands
AU/mL
even
than
6
months
passed
since
Conclusions:
rise
against
novel
longitudinal
follow-up
larger
studies
is
warranted.