Vaccines,
Journal Year:
2023,
Volume and Issue:
11(2), P. 278 - 278
Published: Jan. 28, 2023
This
study
pictures
the
humoral
response
of
100
vaccinees
to
Pfizer/BioNTech
COVID-19
vaccine
over
a
year,
with
particular
focus
on
influence
booster
shot
administered
around
10
months
after
primary
immunization.
The
vaccination
was
assessed
Diasorin’s
SARS-CoV-2
TrimericSpike
IgG.
Abbott’s
Nucleocapsid
IgG
immunoassay
used
identify
contact,
even
asymptomatic.
In
contrast
gradual
decline
anti-spike
between
30
and
240
days
first
dose,
an
increase
noted
360
in
whole
cohort.
However,
statistically
significant
rise
seen
only
boosted
individuals,
this
effect
decreased
time.
An
also
observed
non-boosted
but
recently
infected
participants
decrease
reported
non-boosted,
non-infected
subjects.
These
changes
were
not
significant.
On
day
360,
percentage
new
infections
lower
vs.
subgroups.
immunization
is
most
efficient
way
stimulating
production
anti-spike,
potentially
neutralizing
antibodies.
additionally
enhanced
by
natural
contact
virus.
Individuals
low
level
antibodies
may
benefit
from
dose
administration.
The Journal of Infectious Diseases,
Journal Year:
2022,
Volume and Issue:
226(6), P. 983 - 994
Published: May 10, 2022
Third
coronavirus
disease
2019
(COVID-19)
vaccine
doses
are
broadly
recommended,
but
immunogenicity
data
remain
limited,
particularly
in
older
adults.We
measured
circulating
antibodies
against
the
severe
acute
respiratory
syndrome
2
(SARS-CoV-2)
spike
protein
receptor-binding
domain,
ACE2
displacement,
and
virus
neutralization
ancestral
omicron
(BA.1)
strains
from
prevaccine
up
to
1
month
following
third
dose,
151
adults
aged
24-98
years
who
received
COVID-19
mRNA
vaccines.Following
doses,
humoral
immunity
was
weaker,
less
functional,
durable
adults,
where
a
higher
number
of
chronic
health
conditions
key
correlate
weaker
responses
poorer
durability.
One
after
antibody
concentrations
function
exceeded
post-second-dose
levels,
were
comparable
magnitude
those
younger
at
this
time.
Humoral
universally
than
strain
both
second
doses.
Nevertheless,
3
anti-omicron
reached
equivalence
adults.
conditions,
not
age,
strongest
consistent
responses.Results
underscore
immune
benefits
Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: Feb. 23, 2024
Coronavirus
disease
2019
(COVID-19),
which
is
caused
by
the
novel
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2),
has
a
global
pandemic.
The
Omicron
variant
(B.1.1.529)
was
first
discovered
in
November
2021
specimens
collected
from
Botswana,
South
Africa.
become
dominant
worldwide,
and
several
sublineages
or
subvariants
have
been
identified
recently.
Compared
to
those
of
other
mutants,
most
highly
expressed
amino
acid
mutations,
with
almost
60
mutations
throughout
genome,
are
spike
(S)
protein,
especially
receptor-binding
domain
(RBD).
These
increase
binding
affinity
variants
for
ACE2
receptor,
may
also
lead
immune
escape.
Despite
causing
milder
symptoms,
epidemiological
evidence
suggests
that
exceptionally
higher
transmissibility,
rates
reinfection
greater
spread
than
prototype
strain
as
well
preceding
variants.
Additionally,
overwhelming
amounts
data
suggest
levels
specific
neutralization
antibodies
against
decrease
vaccinated
populations,
although
CD4
+
CD8
T-cell
responses
maintained.
Therefore,
mechanisms
underlying
evasion
still
unclear.
In
this
review,
we
surveyed
current
epidemic
status
potential
escape
Especially,
focused
on
roles
viral
epitope
antigenic
drift,
hybrid
immunity,
“original
sin”
mediating
evasion.
insights
might
supply
more
valuable
concise
information
us
understand
spreading
Human Vaccines & Immunotherapeutics,
Journal Year:
2022,
Volume and Issue:
18(5)
Published: May 2, 2022
There
is
a
wealth
of
data
suggesting
that
the
effectiveness
existing
vaccines
against
Omicron
variant,
most
mutated
SARS-CoV-2
variant
to
date,
has
been
substantially
reduced
if
only
primary
vaccination
administered.
Therefore,
booster
become
topic
current
interest.
We
conducted
comprehensive
search
in
PubMed,
Embase,
and
Cochrane
Library
collect
various
pseudovirus
neutralization
tests
or
live
virus
for
with
serum
specimens
from
vaccinees.
extracted
titers
original
strain,
other
variants
before
after
vaccination,
then
manually
calculated
fold
increase
decrease
relative
variants,
compared
vaccination.
In
two-dose
regimen,
decreased
strain
variants.
However,
both
homologous
heterologous
antibodies
was
significantly
improved,
although
still
lower
than
The
program
based
on
can
produce
broad
but
incomplete
immunity
variant.
MedComm,
Journal Year:
2022,
Volume and Issue:
3(3)
Published: Aug. 16, 2022
Abstract
Since
the
start
of
coronavirus
disease
2019
(COVID‐19)
pandemic,
new
variants
severe
acute
respiratory
syndrome
2
(SARS‑CoV‑2)
have
emerged,
accelerating
spread
virus.
Omicron
was
defined
by
World
Health
Organization
in
November
2021
as
fifth
“variant
concern”
after
Alpha,
Beta,
Gamma,
and
Delta.
In
recent
months,
has
become
main
epidemic
strain.
Studies
shown
that
carries
more
mutations
than
Delta,
wild‐type,
facilitating
immune
escape
its
transmission.
This
review
focuses
on
variant's
origin,
transmission,
biological
features,
subvariants,
mutations,
escape,
vaccination,
detection
methods.
We
also
discuss
appropriate
preventive
therapeutic
measures
should
be
taken
to
address
challenges
posed
variant.
is
valuable
guide
surveillance,
prevention,
development
vaccines
other
therapies
for
variants.
It
desirable
develop
a
efficient
vaccine
against
variant
take
effective
constrain
promote
public
health.
Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: Feb. 2, 2024
Background
Previous
studies
have
demonstrated
enhanced
efficacy
of
vaccine
formulations
that
incorporate
the
chemokine
macrophage
inflammatory
protein
3α
(MIP-3α)
to
direct
antigens
immature
dendritic
cells.
To
address
reduction
in
associated
with
a
mutation
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
mutants,
we
examined
ability
receptor-binding
domain
vaccines
incorporating
MIP-3α
sustain
higher
concentrations
antibody
when
administered
intramuscularly
(IM)
and
more
effectively
elicit
lung
T-cell
responses
intranasally
(IN).
Methods
BALB/c
mice
aged
6–8
weeks
were
immunized
or
DNA
constructs
consisting
SARS-CoV-2
alone
fused
MIP-3α.
In
small-scale
(
n
=
3/group)
experiment,
IM
electroporation
followed
up
for
serum
over
period
1
year
bronchoalveolar
levels
at
termination
study.
Following
IN
immunization
unencapsulated
plasmid
6/group),
evaluated
11
concentrations,
quantities
T
cells
lungs,
IFN-γ-
TNF-α-expressing
antigen-specific
lungs
spleen.
Results
At
12
months
postprimary
vaccination,
recipients
had
significantly,
approximately
threefold,
than
not
The
area-under-the-curve
analyses
12-month
observation
interval
significantly
greater
time
formulation.
immunization,
only
fusion
serum-neutralizing
activity
deemed
be
effective.
After
intranasal
developed
above
those
PBS
controls.
Low
obtained
following
immunization.
Conclusion
Although
requiring
separate
immunizations
optimal
construct
potential
stable
easily
produced
formulation
provide
extended
may
required
protection
setting
emerging
variants.
Without
electroporation,
simple,
uncoated
elicited
responses.
Scientific Reports,
Journal Year:
2022,
Volume and Issue:
12(1)
Published: July 26, 2022
Waning
of
the
immune
response
upon
vaccination
in
SARS-CoV-2
infection
is
an
important
subject
evaluation
this
pandemic,
mostly
healthcare
workers
(HCW)
that
are
constantly
contact
with
infected
samples
and
patients.
Therefore,
our
study
aimed
to
establish
specific
humoral
IgG
IgA
antibodies
vaccination,
during
second
year
pandemic
evaluating
booster
shot
same
vaccine
type.
A
group
103
HCW
documented
exposure
virus
were
monitored
for
levels
prior
after
first
round,
following
8
months
After
post-vaccination
both
decreased,
2.4
times
IgG,
2.7
IgA.
Although
significantly
no
was
registered
group.
shot,
entire
group,
displayed
increased
levels,
immediately
followed
by
increase
post-second
round
statistically
higher
compared
while
restored
at
levels.
Within
or
routine
a
multiple
waves'
generating
new
variants,
populational
immunity
remains
issue
future
implementation
prevention/control
measures.
PLoS ONE,
Journal Year:
2024,
Volume and Issue:
19(4), P. e0298033 - e0298033
Published: April 16, 2024
This
study
determined
the
seropositive
rates
and
levels
of
antibodies
to
severe
acute
respiratory
syndrome
coronavirus-2
in
50
patients
108
vaccinees
using
microneutralization
test
(MNT),
surrogate
virus
neutralization
(sVNT),
chemiluminescent
microparticle
immunoassay
(CMIA),
electrochemiluminescence
(ECLIA).
MNT,
as
reference
method,
employed
living
clade
S
Delta
viruses
measure
neutralizing
(NT)
antibodies,
while
sVNT
wild
type
strain
receptor-binding
domains
(RBD)
antigens
antibodies.
CMIA
ECLIA
only
one
version
RBD
binding
Our
performed
gene
sequencing
exclude
undesired
mutants
that
might
lead
changes
antibody
MNT
assay.
We
showed
spike
protein
amino
acid
sequences
our
contained
13
changes,
with
3
related
reduced
neutralization.
The
assay
a
significant
reduction
patients’
sera
when
variant
replaced
virus.
In
contrast,
by
were
non-significantly
different,
suggesting
could
not
identify
difference
between
antigenicity
RBD.
Furthermore,
correlation
NT
was
moderate
but
modest
post-vaccination
sera.
patients,
or
ECLIA,
different
from
S,
Delta,
all
analyses,
correlations
measured
other
assays
moderate,
r
-values
0.3500–0.7882.
PLoS ONE,
Journal Year:
2024,
Volume and Issue:
19(4), P. e0301367 - e0301367
Published: April 16, 2024
Background
Understanding
the
immune
response
kinetics
to
SARS-CoV-2
infection
and
COVID-19
vaccination
is
important
in
nursing
home
(NH)
residents,
a
high-risk
population.
Methods
An
observational
longitudinal
evaluation
of
37
consenting
vaccinated
NH
residents
with/without
from
October
2020
July
2022
was
conducted
characterize
spike
protein
due
and/or
mRNA
vaccine.
Antibodies
(IgG)
full-length
spike,
nucleocapsid,
receptor
binding
domain
antigens
were
measured,
surrogate
virus
neutralization
capacity
assessed
using
Meso
Scale
Discovery
immunoassays.
The
participant’s
exposure
status
varied
depending
on
acquisition
or
receipt
vaccine
dose.
Longitudinal
linear
mixed
effects
modeling
used
describe
trajectories
based
last
vaccination;
primary
series
considered
two
exposures.
Mean
antibody
titer
values
participants
who
developed
an
post
compared
with
those
did
not.
In
subset
(n
=
15),
memory
B
cell
(MBC)
S-specific
IgG
(%S
IgG)
responses
ELISPOT
assay.
Results
median
age
at
enrollment
70.5
years;
30
(81%)
had
prior
infection,
76%
received
Pfizer-BioNTech
24%
Moderna
homologous
vaccines.
After
observed
augmented
effect
each
exposure,
decline
response,
including
%S
MBCs,
over
time;
percent
decreased
increasing
Participants
least
weeks
post-receipt
have
lower
humoral
levels
than
not
develop
post-receipt.
Conclusions
These
findings
suggest
that
understanding
durability
this
vulnerable
population
can
help
inform
public
health
policy
regarding
timing
booster
vaccinations
as
new
variants
display
escape.