Vaccines,
Год журнала:
2024,
Номер
12(7), С. 801 - 801
Опубликована: Июль 19, 2024
(1)
Background:
Compared
to
medical
personnel,
SARS-CoV-2mRNA
vaccination-related
positive
immunity
rates,
levels,
and
preservation
over
time
in
dialysis
kidney
transplant
patients
are
reduced.
We
hypothesized
that
COVID-19
pre-exposure
influences
both
vaccination-dependent
development
a
group-dependent
manner.
(2)
Methods:
evaluated
2-
9-month
follow-up
data
our
observational
Dia-Vacc
study,
exploring
specific
cellular
(interferon-γ
release
assay
=
IGRA)
and/or
humoral
immune
responses
(IgA/IgG/RBD
antibodies)
after
two
vaccinations
2630
participants,
including
personnel
(301-MP),
(1841-DP),
recipients
(488-KTR).
Study
participants
were
also
separated
into
(hybrid
immunity)
(n
407)
versus
negative
2223)
groups.
(3)
Results:
improved
most
rates
KTR
DP
at
2
months
but
not
MP,
where
reached
almost
100%
independent
of
hybrid
immunity.
In
the
COVID-19-negative
patients’
faded
between
nine
months,
via
percentage
with
an
RBD
antibody
decrease
>50%,
was
markedly
group-
(MP-17.8%,
DP-52.2%,
KTR-38.6%)
vaccine
type-dependent.
contrast,
all
patient
groups
COVID-19,
decreases
>50%
similarly
rare
(MP-4.3%,
DP-7.2%,
KTR-0%)
still
type-dependent,
numerically
reduced
numbers
mRNA-1273-
BNT162b2mRNA-treated
patients.
Multivariable
regression
analysis
changes
by
interval
scale
categorization
confirmed
as
factor
inhibiting
strong
Ab
fading.
MP
T-cell
DP,
symptomatic
(versus
asymptomatic)
identified
reducing
fading
vaccination.
(4)
Conclusions:
After
mRNA
vaccination,
positivity
well
MP/DP/KTR,
prior
infection.
compared
asymptomatic
disease
particularly
effective
blocking
The
emergence
of
new
SARS-CoV-2
variants
and
the
waning
immunity
raise
concerns
about
vaccine
effectiveness
protection
against
COVID-19.
While
antibody
response
has
been
shown
to
correlate
with
risk
infection
original
variant
earlier
concern,
antibody-mediated
Omicron
factors
associated
remain
uncertain.
Nature Communications,
Год журнала:
2024,
Номер
15(1)
Опубликована: Апрель 10, 2024
Several
studies
have
suggested
the
imprinting
of
SARS-CoV-2
immunity
by
original
immune
challenge
without
addressing
formation
de
novo
response
to
successive
antigen
exposures.
As
this
is
crucial
for
development
antigenic
sin,
we
assessed
against
mutated
epitopes
omicron
after
vaccine
breakthrough.
Our
data
demonstrate
a
robust
humoral
in
thrice-vaccinated
individuals
following
breakthrough
which
recall
vaccine-induced
memory.
The
and
memory
B
cell
responses
altered
regions
surface
proteins
are
impaired.
T
spike
protein
present
due
high
cross-reactivity
cells
rather
than
response.
findings,
therefore,
underpin
speculation
that
vaccination
may
lead
sin
if
future
variants
overcome
immunity.
Viruses,
Год журнала:
2024,
Номер
16(5), С. 697 - 697
Опубликована: Апрель 28, 2024
Since
the
SARS-CoV-2
Omicron
virus
has
gained
dominance
worldwide,
its
continual
evolution
with
unpredictable
mutations
and
patterns
revoked
all
authorized
immunotherapeutics.
Rapid
viral
also
necessitated
several
rounds
of
vaccine
updates
in
order
to
provide
adequate
immune
protection.
It
remains
imperative
understand
how
evolves
into
different
subvariants
causes
escape
as
this
could
help
reevaluate
current
intervention
strategies
mostly
implemented
clinics
emergency
measures
counter
pandemic
and,
importantly,
develop
new
solutions.
Here,
we
a
review
focusing
on
major
events
evolution,
including
features
spike
mutation
that
lead
evasion
against
monoclonal
antibody
(mAb)
therapy
vaccination,
suggest
alternative
durable
options
such
ACE2-based
experimental
therapies
superior
mAbs
address
unprecedented
virus.
In
addition,
type
unique
virus-trapping
molecules
can
zoonotic
SARS
coronaviruses,
either
from
unknown
animal
hosts
or
established
wild-life
reservoirs
SARS-CoV-2,
even
seasonal
alpha
coronavirus
NL63
depends
human
ACE2
for
infection.
Journal of Proteome Research,
Год журнала:
2025,
Номер
24(2), С. 515 - 525
Опубликована: Янв. 7, 2025
In
the
past
decade,
a
major
goal
in
biomedical
research
has
been
to
understand
why
individuals
differ
disease
susceptibility,
dynamics,
and
progression.
many
pathologies,
this
variability
stems
from
evolved
immune
mechanisms
that
resist
inflammatory
stress
various
diseases
have
encountered
throughout
life.
These
may
provide
advantages
against
other
diseases,
reduce
comorbidities,
enhance
longevity.
This
study
evaluates
prior
immunity
as
prognostic
factor
COVID-19
patients,
crucial
for
understanding
plasmatic
signaling
cascades
different
stages
their
impact
on
COVID-19,
caused
by
SARS-CoV-2,
primarily
affects
respiratory
system
presents
wide
range
of
symptoms,
posing
significant
challenges
medicine.
systematically
analyzed
inflammation
two
independent
cohorts
infected
patients.
A
serological
profile
is
determined
protein
microarrays,
which
identify
IgM
IgG
responses
37
prevalent
microbial
pathogens
comprehensive
plasma
analysis
21
acute-phase
proteins.
Our
results
reveal
distinct
profiles
correlating
with
severity,
indicating
dysregulation
patients
linked
existing
immunity.
findings
highlight
relevance
monitoring
progression,
particularly
infections
vaccine
failure,
underscore
importance
functional
proteomics
determining
biomarkers.
Emerging Microbes & Infections,
Год журнала:
2025,
Номер
unknown
Опубликована: Фев. 20, 2025
The
unanticipated
emergence
of
the
COVID-19
pandemic
and
rapid
spread
mpox
epidemic
in
2022
2024
brought
unforeseen
challenges
to
public
health.
While
distinct
nature,
these
outbreaks
share
some
similarities
offer
valuable
insights
into
responding
novel
virus
dissemination
vulnerable
populations.
In
light
two
experiences,
we
aim
discern
prioritization
medical
countermeasures
(MCM)
among
antivirals,
antibodies
vaccines.
BMC Infectious Diseases,
Год журнала:
2025,
Номер
25(1)
Опубликована: Фев. 28, 2025
The
continuous
emergence
of
SARS-CoV-2
variants
and
subvariants
poses
significant
public
health
challenges.
latest
designated
subvariant
JN.1,
with
all
its
descendants,
shows
more
than
30
mutations
in
the
spike
gene.
JN.1
has
raised
concerns
due
to
genomic
diversity
potential
enhance
transmissibility
immune
evasion.
This
study
aims
analyse
molecular
characteristics
JN.1-related
lineages
(JN.1*)
identified
Italy
from
October
2023
April
2024
evaluate
neutralization
activity
against
a
subsample
sera
individuals
vaccinated
XBB.1.5
mRNA.
gene
794
JN.1*
strain
was
evaluated
phylogenetic
analysis
conducted
compare
distance
XBB.1.5.
Moreover,
serum
assays
were
performed
on
19
healthcare
workers
(HCWs)
monovalent
mRNA
booster
assess
neutralizing
capacity
JN.1.
Sequence
displayed
high
variability
between
investigation
confirmed
substantial
differentiation
regions
29
shared
mutations,
which
17
located
within
RBD
region.
Pre-booster
observed
42%
HCWs
sera,
increasing
significantly
post-booster,
showing
three
months
after
vaccination.
A
correlation
found
anti-trimeric
Spike
IgG
levels
titers
highlights
Italy.
Results
vaccine
suggested
enhanced
The
emergence
of
COVID-19
necessitated
the
rapid
development
vaccines.
While
highly
effective
at
reducing
severe
disease
and
death,
breakthrough
infections
remain
a
problem
as
virus
continues
to
mutate.
To
help
address
this
issue,
we
show
utility
multiplex
immunoassay
in
measuring
multiple
aspects
antibody
response
generated
by
SARS-CoV-2
We
use
platform
measure
spike-specific
IgG
concentration,
avidity,
receptor-binding
inhibition.
In
addition,
correlate
results
from
an
ACE-2
inhibition
assay
with
corresponding
data
microneutralization
establish
inhibitory
potential
predictor
neutralization.
studied
these
responses
SARS-CoV-2-naïve
-convalescent
vaccinees.
Our
showed
increased
concentrations,
following
vaccination
both
groups.
were
also
able
differentiate
immune
between
two
groups
using
look
diversity.
has
strong
correlations
cell-based
pseudovirus
neutralization
well
WT
Washington
Delta
variant
PRNT50
assays.
This
suggests
that
may
be
simultaneously
predict
different
variants.
Overall,
developed
custom
several
experimental
variations
is
powerful
tool
assessing
vaccinated
individuals.
Vaccines,
Год журнала:
2025,
Номер
13(4), С. 424 - 424
Опубликована: Апрель 17, 2025
Vaccination
has
been
instrumental
in
curbing
the
transmission
of
SARS-CoV-2
and
mitigating
severity
clinical
manifestations
associated
with
COVID-19.
Numerous
COVID-19
vaccines
have
developed
to
this
effect,
including
BioNTech-Pfizer
Moderna’s
mRNA
vaccines,
as
well
adenovirus
vector-based
such
Oxford–AstraZeneca.
However,
emergence
new
variants
subvariants
SARS-CoV-2,
characterized
by
enhanced
transmissibility
immune
evasion,
poses
significant
challenges
efficacy
current
vaccination
strategies.
In
review,
we
aim
comprehensively
outline
landscape
emerging
concern
(VOCs)
sub-lineages
that
recently
surfaced
post-pandemic
years.
We
assess
effectiveness
existing
their
booster
doses,
against
these
subvariants,
BA.2-derived
sub-lineages,
XBB
BA.2.86
(Pirola).
Furthermore,
discuss
latest
advancements
vaccine
technology,
multivalent
pan-coronavirus
approaches,
along
development
several
next-generation
coronavirus
exosome-based,
virus-like
particle
(VLP),
mucosal,
nanomaterial-based
vaccines.
Finally,
highlight
key
critical
areas
for
future
research
address
evolving
threat
develop
strategies
combating
viral
threats,
thereby
improving
preparedness
pandemics.
Frontiers in Immunology,
Год журнала:
2024,
Номер
15
Опубликована: Янв. 31, 2024
Introduction
This
study
sought
to
elucidate
the
long-term
antibody
responses
Moderna
mRNA-1273
COVID-19
vaccine
within
a
Ugandan
cohort,
aiming
contribute
sparse
data
on
m-RNA
immunogenicity
in
Sub-Saharan
Africa.
Methods
We
tracked
development
and
persistence
of
elicited
antibodies
19
participants
aged
18
67,
who
received
two
doses
vaccine.
A
validated
enzyme-linked
immunosorbent
assay
(ELISA)
was
used
quantify
SARS-CoV-2-specific
IgG,
IgM,
IgA
against
spike
(S)
nucleoproteins
(N).
The
study’s
temporal
scope
extended
from
baseline
one
year,
capturing
immediate
immune
responses.
Statistical
analyses
were
performed
using
Wilcoxon
test
evaluate
changes
levels
across
predetermined
intervals
with
Hochberg
correction
for
multiple
comparisons.
Results
Our
results
showed
significant
initial
rise
spike-directed
IgG
(S-IgG)
(S-IgA)
levels,
which
remained
elevated
duration
study.
S-IgG
concentrations
peaked
14
days
afterboosting,
while
IgM
(S-IgM)
transient,
aligning
their
early
response
role.
Notably,
post-booster
did
not
significantly
change.
Prior
status
influenced
post-priming
S-IgA
dynamics,
positive
individuals
maintaining
higher
responses,
difference
that
reach
statistical
post-boost.
Three
instances
breakthrough
infections:
among
exhibited
seropositivity
S-IgG,
participant
initially
seronegative
S-IgG.
Discussion
In
conclusion,
robust
persistent
particularly
after
first
dose,
indicating
potential
immunity.
viral
exposure
enhances
post-vaccination
compared
naive
individuals,
aligned
prior-naïve,
stable
observed
remaining
high
over
an
period,
no
secondary
rise,
by
exposure,
suggest
vaccination
may
sufficiently
prime
system
prolonged
protection
this
population,
allowing
delay
booster
schedules
as
at
time
boosting.
finding
calls
reassessment
dose
scheduling
demographic.