International Immunopharmacology,
Год журнала:
2024,
Номер
143, С. 113362 - 113362
Опубликована: Окт. 18, 2024
Here,
we
report
that
four
functional
fragments
of
the
Severe
Acute
Respiratory
Syndrome
Coronavirus-2
(SARS-CoV-2)
spike
protein
including
receptor
binding
motif
(RBM),
fusion
peptide
(FP),
heptad
repeat
1
(HR1)
and
2
(HR2)
were
chosen
to
develop
a
recombinant
S
subunit
vaccine.
This
consisting
S230
amino
acids
(aa)
(S230)
bound
specifically
antibody
from
COVID-19-patients
serum,
which
showed
very
strong
antigenicity.
The
was
then
engineered
present
on
surface
Hepatitis
B
core
(HBc)
virus-like
particles
(VLPs)
HBc-S230
chimeric
VLPs
Both
vaccines
induced
humoral
cellular
immune
responses
in
mice,
however,
elicited
significantly
higher
immunogenicity
than
S230.
promoted
generate
not
only
dramatically
levels
S230-specific
serum
antibodies,
but
also
marked
CD4+/CD8
+
T
cells
ratio
substantially
yields
IFN-γ
IL-6.
Furthermore,
antibodies
could
effectively
neutralize
infection
with
three
SARS-CoV-2
pseudoviruses
(Wild
type,
Delta
Omicron).
Our
results
demonstrated
immunization
conveyed
immunity,
lasted
longer
six
months.
Clearly,
enhanced
S230,
provide
potent
durable
protection
against
infection,
indicating
possessed
great
potential
for
developing
highly
immunogenic
SARS-CoV-2.
Allergy,
Год журнала:
2022,
Номер
78(2), С. 369 - 388
Опубликована: Ноя. 24, 2022
Abstract
There
has
been
an
important
change
in
the
clinical
characteristics
and
immune
profile
of
Coronavirus
disease
2019
(COVID‐19)
patients
during
pandemic
thanks
to
extensive
vaccination
programs.
Here,
we
highlight
recent
studies
on
COVID‐19,
from
immunological
protective
risk
factors
for
severity
mortality
COVID‐19.
The
efficacy
COVID‐19
vaccines
potential
allergic
reactions
after
administration
are
also
discussed.
occurrence
new
variants
concerns
such
as
Omicron
BA.2,
BA.4,
BA.5
global
have
changed
scenario
Multisystem
inflammatory
syndrome
children
(MIS‐C)
may
cause
severe
heterogeneous
but
with
a
lower
rate.
Perturbations
immunity
T
cells,
B
mast
well
autoantibodies
metabolic
reprogramming
contribute
long‐term
symptoms
is
conflicting
evidence
about
whether
atopic
diseases,
asthma
rhinitis,
associated
susceptibility
better
outcomes
At
beginning
pandemic,
European
Academy
Allergy
Clinical
Immunology
(EAACI)
developed
guidelines
that
provided
timely
information
management
diseases
preventive
measures
reduce
transmission
clinics.
distribution
emerging
acute
respiratory
coronavirus
2
(SARS‐CoV‐2)
reduced
pathogenic
dramatically
decreased
morbidity,
severity,
Nevertheless,
breakthrough
infection
remains
challenge
control.
Hypersensitivity
(HSR)
low
compared
other
vaccines,
these
were
addressed
EAACI
statements
indications
reactions,
including
anaphylaxis
vaccines.
We
gained
depth
knowledge
experience
over
years
since
start
yet
full
eradication
SARS‐CoV‐2
not
horizon.
Novel
strategies
warranted
prevent
high‐risk
groups,
development
MIS‐C
long
Allergy,
Год журнала:
2024,
Номер
79(9), С. 2482 - 2501
Опубликована: Июль 14, 2024
SARS-CoV-2
has
triggered
a
pandemic
and
contributes
to
long-lasting
morbidity.
Several
studies
have
investigated
immediate
cellular
humoral
immune
responses
during
acute
infection.
However,
little
is
known
about
long-term
effects
of
COVID-19
on
the
system.
International Journal of Molecular Sciences,
Год журнала:
2023,
Номер
24(6), С. 5352 - 5352
Опубликована: Март 10, 2023
More
than
three
years
ago,
the
Severe
Acute
Respiratory
Syndrome
Coronavirus
2
(SARS-CoV-2)
caused
unforeseen
COVID-19
pandemic
with
millions
of
deaths.
In
meantime,
SARS-CoV-2
has
become
endemic
and
is
now
part
repertoire
viruses
causing
seasonal
severe
respiratory
infections.
Due
to
several
factors,
among
them
development
immunity
through
natural
infection,
vaccination
current
dominance
seemingly
less
pathogenic
strains
belonging
omicron
lineage,
situation
stabilized.
However,
challenges
remain
possible
new
occurrence
highly
variants
remains
a
threat.
Here
we
review
development,
features
importance
assays
measuring
neutralizing
antibodies
(NAbs).
particular
focus
on
in
vitro
infection
molecular
interaction
studying
binding
receptor
domain
(RBD)
its
cognate
cellular
ACE2.
These
assays,
but
not
measurement
SARS-CoV-2-specific
per
se,
can
inform
us
whether
produced
by
convalescent
or
vaccinated
subjects
may
protect
against
thus
have
potential
predict
risk
becoming
newly
infected.
This
information
extremely
important
given
fact
that
considerable
number
subjects,
vulnerable
persons,
respond
poorly
production
antibodies.
Furthermore,
these
allow
determine
evaluate
virus-neutralizing
capacity
induced
vaccines
administration
plasma-,
immunoglobulin
preparations,
monoclonal
antibodies,
ACE2
synthetic
compounds
be
used
for
therapy
assist
preclinical
evaluation
vaccines.
Both
types
relatively
quickly
adapted
emerging
virus
about
magnitude
cross-neutralization,
which
even
estimate
infected
appearing
variants.
Given
paramount
discuss
their
specific
features,
advantages
disadvantages,
technical
aspects
yet
fully
resolved
issues,
such
as
cut-off
levels
predicting
degree
vivo
protection.
Expert Review of Vaccines,
Год журнала:
2023,
Номер
22(1), С. 422 - 439
Опубликована: Май 10, 2023
Introduction
The
Coronavirus
Disease
2019
(COVID-19)
pandemic
has
caused
devastating
human
and
economic
costs.
Vaccination
is
an
important
step
in
controlling
the
pandemic.
Severe
acute
respiratory
coronavirus-2
(SARS-CoV-2),
causative
agent
of
COVID-19,
infects
cells
by
binding
a
cellular
receptor
through
receptor-binding
domain
(RBD)
within
S1
subunit
spike
(S)
protein.
Viral
entry
membrane
fusion
are
mediated
S2
subunit.Areas
covered
SARS-CoV-2
S
protein,
particularly
RBD,
serves
as
target
for
vaccines.
Here
we
review
structure
function
protein
its
summarize
current
COVID-19
vaccines
targeting
outline
potential
strategies
improving
RBD-based
Overall,
this
provides
information
that
will
facilitate
rational
design
development
safer
more
effective
vaccines.Expert
opinion
harbors
numerous
mutations,
mostly
resulting
multiple
variant
strains.
Although
many
RBD
original
virus
strain
(and
previous
variants)
can
prevent
infection
these
strains,
their
ability
against
recent
dominant
variants,
Omicron
offspring,
significantly
reduced.
Collective
efforts
needed
to
develop
broad-spectrum
control
future
variants
have
potential.
Allergy,
Год журнала:
2022,
Номер
77(8), С. 2431 - 2445
Опубликована: Март 31, 2022
Severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
is
responsible
for
the
ongoing
global
COVID-19
pandemic.
One
possibility
to
control
pandemic
induce
sterilizing
immunity
through
induction
and
maintenance
of
neutralizing
antibodies
preventing
SARS-CoV-2
from
entering
human
cells
replicate
in.
EBioMedicine,
Год журнала:
2023,
Номер
92, С. 104574 - 104574
Опубликована: Май 4, 2023
The
SARS-CoV-2
global
pandemic
has
fuelled
the
generation
of
vaccines
at
an
unprecedented
pace
and
scale.
However,
many
challenges
remain,
including:
emergence
vaccine-resistant
mutant
viruses,
vaccine
stability
during
storage
transport,
waning
vaccine-induced
immunity,
concerns
about
infrequent
adverse
events
associated
with
existing
vaccines.We
report
on
a
protein
subunit
comprising
receptor-binding
domain
(RBD)
ancestral
spike
protein,
dimerised
immunoglobulin
IgG1
Fc
domain.
These
were
tested
in
conjunction
three
different
adjuvants:
TLR2
agonist
R4-Pam2Cys,
NKT
cell
glycolipid
α-Galactosylceramide,
or
MF59®
squalene
oil-in-water
adjuvant,
using
mice,
rats
hamsters.
We
also
developed
RBD-human
RBD
sequence
immuno-evasive
beta
variant
(N501Y,
E484K,
K417N).
as
heterologous
third
dose
booster
following
priming
whole
vaccine.Each
formulation
RBD-Fc
drove
strong
neutralising
antibody
(nAb)
responses
provided
durable
highly
protective
immunity
against
lower
upper
airway
infection
mouse
models
COVID-19.
'beta
variant'
vaccine,
combined
induced
protection
mice
strain
well
strain.
Furthermore,
when
used
booster,
increased
titres
nAb
other
variants
including
alpha,
delta,
delta+,
gamma,
lambda,
mu,
omicron
BA.1,
BA.2
BA.5.These
results
demonstrated
that
subunit/MF59®
adjuvanted
can
induce
high
levels
broadly
reactive
nAbs,
prior
immunisation
ancestral-strain
vaccines.
This
platform
offers
potential
approach
to
augment
some
currently
approved
face
emerging
concern,
it
now
entered
phase
I
clinical
trial.This
work
was
supported
by
grants
from
Medical
Research
Future
Fund
(MRFF)
(2005846),
Jack
Ma
Foundation,
National
Health
Council
Australia
(NHMRC;
1113293)
Singapore
(MOH-COVID19RF-003).
Individual
researchers
NHMRC
Senior
Principal
Fellowship
(1117766),
Investigator
Awards
(2008913
1173871),
Australian
Discovery
Early
Career
Award
(ARC
DECRA;
DE210100705)
philanthropic
awards
IFM
investors
A2
Milk
Company.
Vaccines,
Год журнала:
2023,
Номер
11(4), С. 874 - 874
Опубликована: Апрель 20, 2023
The
vast
majority
of
SARS-CoV-2
vaccines
which
are
licensed
or
under
development
focus
on
the
spike
(S)
protein
and
its
receptor
binding
domain
(RBD).
However,
S
shows
considerable
sequence
variations
among
variants
concern.
aim
this
study
was
to
develop
characterize
a
vaccine
targeting
highly
conserved
nucleocapsid
(N)
protein.
Recombinant
N
expressed
in
Escherichia
coli,
purified
homogeneity
by
chromatography
characterized
SDS-PAGE,
immunoblotting,
mass
spectrometry,
dynamic
light
scattering
differential
scanning
calorimetry.
vaccine,
formulated
as
squalane-based
emulsion,
used
immunize
Balb/c
mice
NOD
SCID
gamma
(NSG)
engrafted
with
human
PBMCs,
rabbits
marmoset
monkeys.
Safety
immunogenicity
assessed
via
ELISA,
cytokine
titer
assays
CFSE
dilution
assays.
protective
effect
studied
SARS-CoV-2-infected
Syrian
hamsters.
Immunization
induced
sustainable
N-specific
IgG
responses
an
mixed
Th1/Th2
response.
In
monkeys,
CD4+/CD8+
T
cell
response
observed.
Vaccinated
hamsters
showed
reduced
lung
histopathology,
lower
virus
proliferation,
weight
relative
body,
faster
body
recovery.
Convacell®
thus
is
shown
be
effective
may
augment
existing
armamentarium
against
COVID-19.
Frontiers in Immunology,
Год журнала:
2024,
Номер
15
Опубликована: Март 27, 2024
Background
The
house
dust
mite
(HDM)
is
widely
recognized
as
the
most
prevalent
allergen
in
allergic
diseases.
Allergen-specific
immunotherapy
(AIT)
has
been
successfully
implemented
clinical
treatment
for
HDM.
Hypoallergenic
B-cell
epitope-based
vaccine
designed
by
artificial
intelligence
(AI)
represents
a
significant
progression
of
recombinant
hypoallergenic
derivatives.
Method
three-dimensional
protein
structure
Der
f
36
was
constructed
using
Alphafold2.
AI-based
tools
were
employed
to
predict
epitopes,
which
subsequently
verified
through
IgE-reaction
testing.
then
synthesized,
expressed,
and
purified.
reduced
allergenicity
assessed
enzyme-linked
immunosorbent
assay
(ELISA),
immunoblotting,
basophil
activation
test.
T-cell
response
evaluated
based
on
cytokine
expression
peripheral
blood
mononuclear
cells
(PBMCs)
patients.
immunogenicity
compared
rabbit
immunization
with
36,
respectively.
inhibitory
effect
blocking
IgG
antibody
specific
IgE-binding
activity
also
examined.
Results
final
selected
non-allergic
epitopes
25–48,
57–67,
107–112,
142–151,
176–184.
showed
reduction
activity.
competitive
inhibition
investigated
only
20%
could
be
achieved,
greatly
when
(98%).
exhibited
low
basophil-stimulating
ratio
similar
that
negative
control,
it
induce
an
increasing
level
IFN‐γ
but
not
Th2
cytokines
IL-5
IL-13
PBMCs.
vaccine-specific
antibodies
inhibit
patients’
IgE
binding
stimulation
Derf
36.
Conclusion
This
study
first
application
AI
strategy
facilitate
development
vaccine,
may
become
promising
HDM-allergic
patients
due
its
high
inducing
IgG.
Journal of Medical Virology,
Год журнала:
2024,
Номер
96(4)
Опубликована: Апрель 1, 2024
This
study
aimed
to
examine
the
safety,
immunogenicity
and
protective
effective
of
inhaled
COVID-19
vaccines
(ICVs).
Literature
research
was
done
through
EMBASE,
Cochrane,
PubMed,
Web
Science
up
10
March
2024.
Pooled
estimates
with
corresponding
95%
confidence
intervals
(CI)
were
computed
compared
using
random
effects
common
model.
Of
15
studies,
11
analyzed
13
immunogenicity,
3
effective.
The
results
showed
a
favorable
safety
profile
ICVs
for
primary
vaccination
series,
however
it
does
not
always
seem
produce
expected
immune
response
Meta-analysis
booster
vaccinations
(BVs)
that
levels
neutralizing
antibody
Geometric
mean
titer
(nAb-GMT)
aerosolised
Ad5-nCoV
(AAd5-nCoV)
all
higher
than
those
inactivated
vaccine
(INA-nCoV)
(standard
difference
(SMD)
=
2.32;
CI:
1.96-2.69)
intramuscular
(IMAd5-nCoV)
(SMD
0.31;
0.14-0.48)
against
original
strain
SARS-CoV-2.
Importantly,
we
also
observed
similar
in
omicron
variant.
In
addition,
ICV
BVs
has
high
mucosal
immunity
IgA
antibodies.
risk
adverse
events
comparable
or
lower
AAd5-nCoV
INA-nCoV
IMAd5-nCoV.
Current
evidence
shows
well.
dose
had
(including
immunity)
provided
protection
caused
by
SARS-CoV-2
Further
studies
are
needed
investigate
long-term
intranasal
various
types
ICVs.