medRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2024,
Номер
unknown
Опубликована: Май 28, 2024
Abstract
People
living
with
HIV
(PLWH)
despite
having
appreciable
depletion
of
CD4
+
T-cell
show
a
good
SARS-
CoV-2
vaccination
response.
The
underlying
mechanism(s)
are
currently
not
understood.
We
studied
serological
and
polyfunctional
responses
in
PLWH
receiving
anti-retroviral
therapy
stratified
on
counts
as
PLWH-high
(CD4
≥500
cells/μL)
PLWH-low
(<500
cells/μL).
Responses
were
assessed
longitudinally
before
the
first
(T0),
1-month
after
dose
(T1),
3-
months
(T2),
6-months
(T3)
second
dose.
Expectedly,
both
-low
groups
developed
similar
T2,
which
also
non-significantly
different
to
age
vaccination-matched
HIV-negative
controls
at
T3.
IgG
titers
protective
showing
correlation
ACE2-neutralizations
(R=0.628,
P=0.005).
While
no
difference
T3
was
observed
between
activated
CD154
memory
T-cells,
spike-
specific
cytokine
expression
analysis
showed
that
preferentially
express
IL-2
(P<0.001)
controls,
IFN-γ
(P=0.017).
negatively
correlated
IL-2-
expressing
T-cells
including
(Spearman
ρ:
-0.85
-0.80,
respectively;
P<0.001).
Our
results
suggest
durable
developing
vaccinated
associated
IL-2-mediated
activation
likely
compensates
for
PLWH.
Immunosenescence
increases
the
risk
and
severity
of
diseases
in
elderly
individuals
leads
to
impaired
vaccine-induced
immunity.
With
aging
global
population
emerging
epidemics,
developing
adjuvants
vaccines
for
improve
their
immune
protection
is
pivotal
healthy
worldwide.
Deepening
our
understanding
role
immunosenescence
vaccine
efficacy
could
accelerate
research
focused
on
optimizing
delivery
individuals.
In
this
review,
we
analyzed
characteristics
at
cellular
molecular
levels.
Strategies
vaccination
potency
are
summarized,
including
increasing
antigen
dose,
preparing
multivalent
vaccines,
adding
appropriate
adjuvants,
inhibiting
chronic
inflammation,
immunosenescence.
We
hope
that
review
can
provide
a
new
findings
with
regards
impacts
vaccine-mediated
inspire
development
individualized
Human Vaccines & Immunotherapeutics,
Год журнала:
2024,
Номер
20(1)
Опубликована: Авг. 16, 2024
Immune
imprinting
is
a
phenomenon
that
stems
from
the
fundamentals
of
immunological
memory.
Upon
recurrent
exposures
to
an
evolving
pathogen,
immune
system
must
weigh
benefits
rapidly
recalling
established
antibody
repertoires
with
greater
affinity
initial
variant
or
invest
additional
time
and
energy
in
producing
de
novo
responses
specific
emerging
variant.
In
this
review,
we
delve
into
mechanistic
complexities
its
role
shaping
subsequent
responses,
both
recall,
against
respiratory
viruses
such
as
influenza
coronaviruses.
By
exploring
duality
imprinting,
examine
potential
enhance
hinder
protection
disease,
while
emphasizing
host
viral
factors.
Finally,
explore
how
different
vaccine
platforms
may
affect
comment
on
strategies
can
favor
variant-specific
responses.
Signal Transduction and Targeted Therapy,
Год журнала:
2025,
Номер
10(1)
Опубликована: Фев. 25, 2025
Abstract
The
emergence
of
XBB-
and
JN.1-lineages
with
remarkable
immune
evasion
characteristics
have
led
to
rises
in
breakthrough
infections
within
populations.
In
addition,
the
unfavorable
impacts
imprinting,
stemming
from
continuous
exposure
antigens
circulated
viruses,
been
observed
incline
response
against
earlier
lineages,
thereby
declining
neutralization
newly
emerged
Omicron
subvariants.
this,
advancement
next-generation
vaccines
COVID-19
targeting
components
new
subvariants
such
as
XBB-lineage
is
imperative.
current
study,
a
self-assembled
trimeric
recombinant
protein
(RBD
XBB.1.5
-HR)
was
generated
by
concatenating
sequences
receptor
binding
domain
(RBD)
derived
heptad-repeat
1
(HR1)
HR2
spike
S2
subunit.
Adjuvanted-RBD
-HR
induced
robust
humoral
cellular
responses,
characterized
elevated
JN.1-inculuded
substantial
population
antigen-specific
T
memory
cells.
Protective
immunity
conferred
RBD
vaccine
preserved
post-immunization,
evidenced
germinal
center
B
(GC
B)
follicular
helper
(Tfh)
sustained
potency,
an
increase
cells
(MBCs)
long-lived
plasma
(LLPCs).
showed
favorable
boosting
effect
when
administered
heterologously
after
three
doses
inactivated
virus
(IV)
mRNA
vaccines.
Significantly,
it
provided
protection
live
EG.5.1
viruses
vivo.
monovalent
safety
immunogenicity,
neutralizing
antibodies
JN.1-
individuals
prior
vaccinations.
These
findings
highlight
its
clinical
potential
safeguarding
circulating
Nature Communications,
Год журнала:
2024,
Номер
15(1)
Опубликована: Июль 3, 2024
Abstract
As
the
new
SARS-CoV-2
Omicron
variants
and
subvariants
emerge,
there
is
an
urgency
to
develop
intranasal,
broadly
protective
vaccines.
Here,
we
developed
highly
efficacious,
intranasal
trivalent
vaccine
candidates
(TVC)
based
on
three
components
of
MMR
vaccine:
measles
virus
(MeV),
mumps
(MuV)
Jeryl
Lynn
(JL1)
strain,
MuV
JL2
strain.
Specifically,
MeV,
MuV-JL1,
MuV-JL2
strains,
each
expressing
prefusion
spike
(preS-6P)
from
a
different
variant
concern
(VoC),
were
combined
generate
TVCs.
Intranasal
immunization
IFNAR1
−/−
mice
female
hamsters
with
TVCs
generated
high
levels
S-specific
serum
IgG
antibodies,
broad
neutralizing
mucosal
IgA
antibodies
as
well
tissue-resident
memory
T
cells
in
lungs.
The
immunized
protected
challenge
original
WA1,
B.1.617.2,
B.1.1.529
strains.
preexisting
MeV
immunity
does
not
significantly
interfere
efficacy
TVC.
Thus,
platform
promising
next-generation
candidate.
European journal of medical research,
Год журнала:
2025,
Номер
30(1)
Опубликована: Янв. 6, 2025
The
SARS-CoV-2
Omicron
variant,
since
its
initial
detection,
has
rapidly
spread
across
the
globe,
becoming
dominant
strain.
It
is
important
to
study
immune
response
of
variant
due
remarkable
ability
escape
majority
existing
neutralizing
antibodies.
surge
in
infections
among
most
Chinese
residents
by
end
2022
provides
a
unique
opportunity
understand
system's
populations
with
limited
exposure
prior
variants.
We
tested
levels
IgG,
IgA,
and
IgM
specific
prototype
RBD
(receptor-binding
domain)
blood
samples
from
636
individuals
chemical
luminescence
assay,
ELISA
pseudovirus-based
neutralization
assay.
Inoculation
inactivated
vaccines
or
recombinant
protein
showed
higher
IgG
after
infection
than
unvaccinated
individuals.
Moreover,
age
resulted
different
as
level
patients
aged
>
60
years
was
lower
that
<
years.
This
indicates
induced
breakthrough
between
old
young
found
booster
dose
vaccine
led
significant
increase
against
helped
induce
antibodies
BA.5
BF.7
variants
an
individuals,
which
previous
report
on
older
people.
These
data
suggest
vaccination
helps
high
Trial
registration:
purely
observational
study.
Research Square (Research Square),
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 8, 2025
Abstract
The
objective
of
this
study
was
to
investigate
the
features
immune
protection
against
SARS-CoV-2
infection
in
a
single
cohort
during
6–17
months
following
booster
immunization
with
an
mRNA-based
vaccine.
results
illustrate
influence
humoral
and
cellular
immunity
on
efficacy
Notably,
neutralizing
antibody
titers
were
found
serve
as
reasonably
reliable
correlate
prior
immunization.
However,
predictive
power
largely
lost
after
boosting.
loss
appears
be
due
critical
remodeling
response
Our
findings
support
hypothesis
that
both
conserved
non-conserved
epitopes
viral
Spike
protein's
receptor-binding
domain
(RBD)
is
crucial
for
optimal
long-term
Omicron
infection.
While
may
provide
cross-variant
protection,
antibodies
targeting
RBD
play
pivotal
role
achieving
maximum
protection.
These
observations
highlight
repeated
shaping
landscape
reinforce
necessity
considering
components,
alongside
intended
use
considerations,
when
assessing
vaccine
developing
future
strategies.
Vaccines,
Год журнала:
2025,
Номер
13(2), С. 101 - 101
Опубликована: Янв. 21, 2025
Background/Objectives:
Understanding
the
behavior
of
B
cells
during
infection
and
vaccination
is
important
for
determining
protective
humoral
immunity.
We
evaluated
profile
immunity
cell
pool
in
individuals
who
were
acutely
infected
with
SARS-CoV-2,
recovered
from
COVID-19,
or
received
two
doses
AZD1222
vaccine.
Methods:
Peripheral
blood
mononuclear
(PBMCs)
these
subjected
to
vitro
stimulation
promote
differentiation
into
antibody-secreting
(ASCs),
ELISpot
abundance
pan
SARS-CoV-2
Spike
S1-reactive
IgG+
ASC.
Stimulated
PBMCs
characterized
using
flow
cytometry.
Culture
supernatants
assessed
soluble
B-cell-activating
factors.
The
IgA
IgG
S1
through
ELISA.
Results:
displayed
a
robust
ASC
compared
acute
vaccinated
individuals.
Although
frequency
total
subsets
did
not
vary
among
groups,
plasmablast
increased
naïve
double-negative
acute,
recovered,
Similar
production
appeared
be
present
During
vaccination,
more
produced
than
IgA.
In
patients,
BAFF
levels
positively
correlated
but
negatively
IgA+
cells.
Conclusions:
Vaccination
natural
COVID-19
induce
differential
functionality
suggest
that
new
vaccines
against
incorporate
molecular
adjuvants
regulate
lymphocyte
consider
beneficial
aspects
response
addition
IgG.
One Health Journal,
Год журнала:
2025,
Номер
3(I), С. 5 - 21
Опубликована: Янв. 25, 2025
Over
a
period
of
5
years,
the
emergent
SARS-CoV-2
virus
underwent
process
adaptation
to
human
body
as
species
host
and
acquired
evolutionary
changes
that
bring
it
closer
routine
respiratory
viruses
in
terms
epidemic
clinical
characteristics.
The
work
presents
systematized
information
on
molecular
genetics
antigenic
characteristics
variants
virus,
categories
their
potential
danger
with
detailed
description
spike
mutations
current
sub-variants
Omicron
(Variants
Interest
(VOI)
-
BA.2.86,
JN.1;
Variants
under
Monitoring
(VUM)
JN.1.7,
JN.1.18,
KP.2,
KP.3,
KP.3.1.1,
LB.1
XEC)
its
de-escalated
subvariants.
effect
some
or
combinations
properties
is
characterized.
trends
prevalence
priority
VOI
VUM
world
are
estimated
trend
rapid
increase
intensity
circulation
KP.3.1.1
XEC
against
background
decrease
other
fall
2024
shown.
issue
immune
imprinting
for
COVID-19
associated
both
natural
infection
vaccination
depending
vaccine
strain
considered.
characterization
FDA-recommended
vaccines
2024/2025
season
provided,
taking
into
account
manufacturing
technology,
strains,
purpose.
Based
analysis
data
effectiveness
relation
risks
infection,
severity
course
disease
mortality,
need
vaccinate
individuals
only
from
risk
groups,
is,
according
medical
age
indications,
emphasized
order
reduce
mortality.
However,
composition
these
must
correspond
epidemically
relevant
virus.
Journal of Nanobiotechnology,
Год журнала:
2025,
Номер
23(1)
Опубликована: Фев. 18, 2025
The
continuous
emergence
of
severe
acute
respiratory
syndrome
coronavirus-2
(SARS-CoV-2)
variants
highlights
the
need
to
update
coronavirus
2019
disease
(COVID-19)
vaccine
components.
Epitope-based
designs
targeting
conserved
and
immunorecessive
regions
SARS-CoV-2
are
critically
needed.
Here,
we
report
an
engineered
epitope-focused
immunogen
design
based
on
a
novel
horseshoe-shaped
natural
protein
scaffold,
named
ribonuclease
inhibitor
1
(RNH1),
that
can
multiply
display
neutralizing
epitopes
from
S2
stem
helix.
designed
RNH1-S1139
demonstrates
high
binding
affinity
S2-specific
antibodies
elicits
robust
epitope-targeted
antibody
responses
either
through
homologous
or
heterologous
vaccination
regimens.
immune
serum
has
been
proven
have
similar
ability
against
SARS-CoV,
its
variants,
providing
broad-spectrum
protection
as
membrane
fusion
inhibitor.
Further
studies
showed
RNH1
potential
serve
versatile
scaffold
displays
other
helical
various
antigens,
including
syncytial
virus
(RSV)
F
glycoprotein.
Our
proposed
engineering
strategy
via
tailored
horseshoe-shape
nano-scaffold
supports
continued
development
vaccines
part
next-generation
design.
Journal of Medical Virology,
Год журнала:
2025,
Номер
97(2)
Опубликована: Фев. 1, 2025
Multiple
studies
demonstrate
the
existence
of
attenuated
neutralizing
activity
to
Omicron
variants
in
original
SARS-CoV-2
strain
vaccinated
population
undergoing
breakthrough
infection,
which
reflects
a
phenomenon
immune
imprinting
humoral
immunity.
Herein,
through
designing
spike
protein
peptide
pools
from
four
subvariants
and
wild
type
(WT)
counterpart,
we
intended
determine
antiviral
T
cell
immunoreactivity
Omicron-infected
COVID-19
patients
with
or
without
previous
vaccination.
We
have
demonstrated
that
IFN-γ
producing
cells
against
subvariants-derived
were
significantly
less
than
those
WT
counterpart
BA.5/BA.7
infected
receiving
inactivated
vaccination
whereas
comparable
unvaccinated
group.
Notably,
reinfection
restored
viral-specific
immunity
strains
individuals.
Therefore,
similar
strain-derived
vaccines
induces
when
infection.
Since
can
restore
strains,
it
is
necessary
design
multivalent
immunogens
for
vaccine
development
overcome
both
B
other
highly
mutant
pathogens.