Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: Dec. 10, 2024
Throughout
the
COVID-19
pandemic,
emergence
of
new
viral
variants
has
challenged
public
health
efforts,
often
evading
antibody
responses
generated
by
infections
and
vaccinations.
This
immune
escape
led
to
waves
breakthrough
infections,
raising
questions
about
efficacy
durability
protection.
Here
we
focus
on
impact
SARS-CoV-2
Delta
Omicron
spike
mutations
ACE-2
receptor
binding,
protein
stability,
response
evasion.
had
3-5
times
higher
binding
affinities
than
ancestral
strain
(KD
Nature Communications,
Journal Year:
2023,
Volume and Issue:
14(1)
Published: Sept. 12, 2023
The
heterogeneity
of
the
SARS-CoV-2
immune
responses
has
become
considerably
more
complex
over
time
and
diverse
imprinting
is
observed
in
vaccinated
individuals.
Despite
vaccination,
following
emergence
Omicron
variant,
some
individuals
appear
susceptible
to
primary
infections
reinfections
than
others,
underscoring
need
elucidate
how
are
influenced
by
previous
vaccination.
IgG,
IgA,
neutralizing
antibodies
T-cell
1,325
(955
which
were
infection-naive)
investigated
before
after
three
doses
BNT162b2
vaccine,
examining
their
relation
breakthrough
context
Omicron.
Our
study
shows
that
both
humoral
cellular
vaccination
generally
higher
infection
compared
infection-naive.
Notably,
viral
exposure
was
crucial
achieving
a
robust
IgA
response.
Individuals
with
lower
antibody
postvaccination
had
significantly
risk
reinfection
future
infections.
This
not
for
responses.
A
subsequent
dampened
infection,
consistent
imprinting.
These
results
underscore
significant
impact
hybrid
immunity
general,
particularly
even
revaccination,
importance
preventing
Vaccine,
Journal Year:
2023,
Volume and Issue:
41(27), P. 4042 - 4049
Published: April 10, 2023
Coronavirus
disease-2019
(COVID-19)
is
an
ongoing
pandemic
caused
by
the
newly
emerged
virus
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2).
Currently,
COVID-19
vaccines
are
given
intramuscularly
and
they
have
been
shown
to
evoke
systemic
immune
responses
that
highly
efficacious
towards
preventing
disease
death.
However,
vaccine-induced
immunity
wanes
within
a
short
time,
booster
doses
currently
recommended.
Furthermore,
current
vaccine
formulations
do
not
adequately
restrict
infection
at
mucosal
sites,
such
as
in
nasopharyngeal
tract
and,
therefore,
limited
capacity
block
transmission.
With
these
challenges
mind,
several
being
developed
with
aim
of
inducing
long-lasting
protective
sites
where
SARS-COV-2
begins.
Past
successes
vaccinations
underscore
potential
developmental
stage
SARS-CoV-2
reduce
burden,
if
eliminate
it
altogether.
Here,
we
discuss
triggered
recent
advances
our
understanding
induced
vaccines.
We
also
highlight
or
tested
for
human
use
vaccination.
Scientific Reports,
Journal Year:
2023,
Volume and Issue:
13(1)
Published: Jan. 23, 2023
Abstract
Coronavirus
disease
2019
(COVID-19)
is
caused
by
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2).
We
evaluated
the
anti-SARS-CoV-2
antibody
levels,
anti-spike
(S)-immunoglobulin
G
(IgG)
and
anti-nucleocapsid
(N)-IgG,
neutralization
activity
of
IgG
in
COVID‑19‑convalescent
plasma
against
variants
SARS-CoV-2,
alpha,
beta,
gamma,
delta,
kappa,
omicron
R.1
strains.
The
study
included
30
patients
with
clinically
diagnosed
COVID-19.
anti-S-IgG
anti-N-IgG
levels
ranged
from
30.0
to
555.1
10.1
752.6,
respectively.
(50%
inhibition
concentration:
IC
50
)
for
wild-type
Wuhan
strain
<
6.3
81.5
µg/ml.
antibodies
were
>
100
µg/ml
18
(60%)
subjects
infected
beta
variant.
values
correlated
inversely
(
p
0.05),
but
no
such
correlation
was
noted
anti-N-IgG.
prevented
infectivity
cytopathic
effects
six
different
concern
cell-based
assays
wild-type,
kappa
strains,
not
that
considered
main
neutralizing
blood,
although
other
factors
may
be
important
body
tissues.
Journal of Controlled Release,
Journal Year:
2024,
Volume and Issue:
371, P. 179 - 192
Published: May 29, 2024
The
delivery
of
vaccines
plays
a
pivotal
role
in
influencing
the
strength
and
longevity
immune
response
controlling
reactogenicity.
Mucosal
immunization,
as
compared
to
parenteral
vaccination,
could
offer
greater
protection
against
respiratory
infections
while
being
less
invasive.
While
oral
vaccination
has
been
presumed
effective
believed
target
mainly
gastrointestinal
tract,
trans-buccal
using
mucoadhesive
films
(MAF)
may
allow
targeted
mucosa.
Here
we
present
an
strategy
for
mucosal
several
vaccine
platforms
incorporated
MAF,
including
DNA
plasmids,
viral
vectors,
lipid
nanoparticles
incorporating
mRNA
(mRNA/LNP).
mRNA/LNP
formulation
targeting
SARS-CoV-2
proof
concept
remained
stable
within
MAF
consisting
slowly
releasing
water-soluble
polymers
impermeable
backing
layer,
facilitating
enhanced
penetration
into
This
elicited
antibody
cellular
responses
comparable
intramuscular
injection,
but
also
induced
production
IgAs,
highlighting
its
efficacy,
particularly
use
booster
potential
advantage
infections.
preparation
demonstrates
significant
advantages,
such
efficient
delivery,
stability,
simple
noninvasive
administration
with
alleviate
hesitancy.
Microbiology and Immunology,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 9, 2025
The
intranasal
vaccine
against
coronavirus
disease
2019
(COVID-19)
has
gained
more
attention
because
of
its
ability
to
induce
both
mucosal
and
systemic
immune
responses.
We
have
recently
developed
a
c-GAMP-adjuvanted
bivalent
receptor-binding
domain
(RBD)
vaccine,
derived
from
the
ancestral
strain
Omicron
variant.
demonstrated
here
that
administration
this
candidate
triggers
not
only
respiratory
but
also
response
SARS-CoV-2.
immunized
mice
elicited
broadly
neutralizing
antibodies
(Wuhan-1)
variants
concern
(Delta,
BA.1,
BA.5).
This
route
vaccination
induced
potent
T
cell
responses
with
strong
cytotoxic
activity
Wuhan-1
BA.1
strains.
Additionally,
intranasally
significantly
suppressed
SARS-CoV-2
RNA
levels
in
circulation
spleens,
indicating
effective
containment
virus
beyond
tract.
These
findings
suggest
RBD
holds
promise
for
combating
infections.
Canadian Journal of Infectious Diseases and Medical Microbiology,
Journal Year:
2024,
Volume and Issue:
2024, P. 1 - 8
Published: Feb. 14, 2024
Background.
Severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
is
the
virus
that
causes
disease
2019
(COVID-19).
It
estimated
more
than
half
of
new
infections
are
transmitted
by
asymptomatic
people;
therefore,
isolation
symptomatic
people
not
enough
to
control
spread
disease.
Methods.
A
total
171
unvaccinated
young
adults
(18–35
years)
from
Sonora,
Mexico,
who
underwent
a
structured
survey
identify
prior
COVID-19
infections,
were
included
in
this
study.
qualitative
determination
anti-SARS-CoV-2
antibodies
serum
was
performed
lateral
flow
immunoassay
(Certum
IgG/IgM
Rapid
Test™
cassette
kit)
and
neutralizing
also
determined
(GenScript
cPass
assay).
Results.
36
reported
history
infection,
135
no
COVID-19.
In
contrast,
49.6%
(67/135)
individuals
had
previous
SARS-CoV-2
infection
seropositive
rapid
antibody
test,
48.1%
(65/135)
them
antibodies.
Conclusions.
These
results
suggest
adults,
could
be
high
percentage
individuals,
which
contribute
part
slow
current
pandemic
due
large
number
cases
contagious
silent
virus.
Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: Feb. 16, 2024
This
study
aimed
to
delineate
longitudinal
antibody
responses
the
Pfizer-BioNTech
BNT162b2
COVID-19
vaccine
within
Ugandan
subset
of
Sub-Saharan
African
(SSA)
demographic,
filling
a
significant
gap
in
global
datasets.
We
enrolled
48
participants
and
collected
320
specimens
over
12
months
after
primary
vaccination
dose.
A
validated
enzyme-linked
immunosorbent
assay
(ELISA)
was
used
quantify
SARS-CoV-2-specific
IgG,
IgM,
IgA
concentrations
(ng/ml)
optical
densities
(ODs).
Statistical
analyses
included
box
plots,
diverging
bar
graphs,
Wilcoxon
test
with
Bonferroni
correction.
noted
robust
S-IgG
response
14
days
dose,
which
consistent
data.
There
no
surge
levels
booster
contrasting
trends
other
populations.
The
S-IgM
transient
predominantly
below
established
thresholds
for
this
population,
reflects
its
typical
early
emergence
rapid
decline.
S-IgA
rose
initial
dose
then
decreased
six
months,
aligning
temporal
patterns
mucosal
immunity.
Eleven
breakthrough
infections
were
noted,
all
asymptomatic,
regardless
participants'
serostatus,
suggests
protective
effect
from
vaccination.
elicited
strong
SSA
demographic.
dynamics
distinctly
differed
data
highlighting
significance
region-specific
research
necessity
customised
strategies.
PLoS ONE,
Journal Year:
2024,
Volume and Issue:
19(7), P. e0307568 - e0307568
Published: July 25, 2024
COVID-19
disproportionately
affected
minorities,
while
research
barriers
to
engage
underserved
communities
persist.
Serological
studies
reveal
infection
and
vaccination
histories
within
these
communities,
however
lack
of
consensus
on
downstream
evaluation
methods
impede
meta-analyses
dampen
the
broader
public
health
impact.
To
impact
vaccine
uptake
among
diverse
develop
rigorous
serological
methods,
we
engaged
racial
ethnic
minorities
in
Massachusetts
a
cross-sectional
study
(April—July
2022),
screened
blood
saliva
for
SARS-CoV-2
human
endemic
coronavirus
(hCoV)
antibodies
by
bead-based
multiplex
assay
point-of-care
(POC)
test
developed
across-plate
normalization
classification
boundary
optimal
qualitative
assessments.
Among
290
participants,
91.4%
reported
receiving
at
least
one
dose
vaccine,
41.7%
past
infections,
which
was
confirmed
POC-
multiplex-based
IgG
seroprevalences.
We
found
significant
differences
antigen-specific
IgA
antibody
outcomes
indication
cross-reactivity
with
hCoV
OC43.
Finally,
26.5%
participants
lingering
symptoms,
mostly
middle-aged
Latinas.
Hence,
prolonged
symptoms
were
common
our
population
require
attention,
despite
high
uptake.
Saliva
served
as
less-invasive
sample-type
IgG-based
serosurveys
needed
be
evaluated
reliable
serosurvey
results.
The
use
assessment
will
help
standardize
future
beyond
SARS-CoV-2.