Journal of Biomedical Science,
Journal Year:
2022,
Volume and Issue:
29(1)
Published: July 7, 2022
With
the
continuous
emergence
of
new
SARS-CoV-2
variants
that
feature
increased
transmission
and
immune
escape,
there
is
an
urgent
demand
for
a
better
vaccine
design
will
provide
broader
neutralizing
efficacy.We
report
mRNA-based
using
engineered
"hybrid"
receptor
binding
domain
(RBD)
contains
all
16
point-mutations
shown
in
currently
prevailing
Omicron
Delta
variants.A
booster
dose
hybrid
mice
previously
immunized
with
wild-type
RBD
induced
high
titers
broadly
antibodies
against
tested
concern
(VOCs).
In
naïve
mice,
generated
strong
Omicron-specific
as
well
low
but
significant
other
VOCs.
Hybrid
also
elicited
CD8+/IFN-γ+
T
cell
responses
conserved
epitope
present
wild
type
VOCs.These
results
demonstrate
inclusion
different
antigenic
mutations
from
various
feasible
approach
to
develop
cross-protective
vaccines.
Immunity,
Journal Year:
2023,
Volume and Issue:
56(4), P. 864 - 878.e4
Published: March 16, 2023
T
cells
are
a
critical
component
of
the
response
to
SARS-CoV-2,
but
their
kinetics
after
infection
and
vaccination
insufficiently
understood.
Using
"spheromer"
peptide-MHC
multimer
reagents,
we
analyzed
healthy
subjects
receiving
two
doses
Pfizer/BioNTech
BNT162b2
vaccine.
Vaccination
resulted
in
robust
spike-specific
cell
responses
for
dominant
CD4
Journal of Clinical Investigation,
Journal Year:
2023,
Volume and Issue:
133(10)
Published: March 23, 2023
BackgroundMaintaining
durable
immunity
following
vaccination
represents
a
major
challenge,
but
whether
mRNA
booster
improves
durability
is
unknown.MethodsWe
measured
antibody
responses
in
55
healthy
adults,
who
received
dose
of
the
Pfizer-BioNTech
or
Moderna
vaccine
against
SARS-CoV-2
and
calculated
half-life
titers.
We
also
memory
B
T
cell
subset
28
participants.
In
13
volunteers
second
vaccine,
we
serum
titers
responses.ResultsThe
(third
immunization)
at
6
to
10
months
increased
serum-neutralizing
(nAb)
76
days
from
56
66
after
primary
2-dose
vaccination.
A
(fourth
year
further
88
days.
However,
despite
this
modestly
improved
nAb
ancestral
(WA.1)
strain,
there
was
loss
neutralization
capacity
Omicron
subvariants
BA.2.75.2,
BQ.1.1,
XBB.1.5
(48-,
71-,
66-fold
drop
titers,
respectively,
relative
WA.1
strain).
Although
only
45%
65%
participants
demonstrated
detectable
titer
newer
variants
dose),
response
declined
below
detection
limit
almost
all
individuals
by
months.
contrast,
induced
antigen-specific
cells
that
persisted
for
least
months.ConclusionThe
marginally
immunizations
with
vaccines.
Nature Immunology,
Journal Year:
2024,
Volume and Issue:
25(4), P. 633 - 643
Published: March 14, 2024
Abstract
Vaccines
have
reduced
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
morbidity
and
mortality,
yet
emerging
variants
challenge
their
effectiveness.
The
prevailing
approach
to
updating
vaccines
targets
the
antibody
response,
operating
under
presumption
that
it
is
primary
defense
mechanism
following
vaccination
or
infection.
This
perspective,
however,
can
overlook
role
of
T
cells,
particularly
when
levels
are
low
absent.
Here
we
show,
through
studies
in
mouse
models
lacking
antibodies
but
maintaining
functional
B
cells
lymphoid
organs,
immunity
conferred
by
prior
infection
mRNA
protect
against
SARS-CoV-2
independently
antibodies.
Our
findings,
using
three
distinct
inclusive
a
novel
human/mouse
ACE2
hybrid,
highlight
CD8
+
essential
for
combating
infections,
whereas
CD4
contribute
managing
milder
cases,
with
interferon-γ
having
an
important
function
this
antibody-independent
defense.
These
findings
importance
cell
responses
vaccine
development,
urging
broader
perspective
on
protective
beyond
just
Metabolism Open,
Journal Year:
2022,
Volume and Issue:
14, P. 100180 - 100180
Published: March 17, 2022
Vaccination
programs
against
SARS-CoV-2
constitute
the
mainstay
of
public
health
interventions
global
COVID-19
pandemic.
Currently
available
vaccines
have
shown
90%
or
better
rates
protection
severe
disease
and
mortality.
Barely
a
year
after
became
available,
Omicron
variant
its
unprecedented
speed
transmission
has
posed
new
challenge.
Overall,
presents
increased
immune
escape,
transmissibility,
decreased
pathogenicity.
Vaccines
do
not
offer
full
acquisition,
since
"breakthrough"
infections
may
occur
in
fully
vaccinated
individuals,
who
turn
spread
virus
to
others.
Breakthrough
be
causally
related
viral
profile
(viral
load,
incubation
period,
pathogenicity,
evasion),
immunity
characteristics
(mucosal
versus
systemic
immunity,
duration
etc.),
host
determinants
(age,
comorbidities,
status,
immunosuppressive
drugs)
vaccination
properties
(platform,
antigen
dose,
dose
number,
interval,
route
administration).
Determining
rate
breakthrough
challenging
necessitates
conduction
population-based
studies
regarding
vaccine
effectiveness
as
well
neutralizing
antibody
testing,
surrogate
protection.
In
this
review,
we
analyze
causes
infections,
their
clinical
consequences
(severity
infection
transmission),
methods
determining
incidence
challenges
perspectives.
Long
COVID
multi-inflammatory
syndrome
adolescents
significantly
reduced
infections.
The
need
for
universal
pancoranavirus
that
would
aim
at
protecting
plethora
variants
emerging
is
discussed.
Finally,
novel
strategies,
such
nasal
vaccines,
confer
robust
mucosal
protection,
reducing
efficiently
transmission.
Chemical Biology & Drug Design,
Journal Year:
2022,
Volume and Issue:
99(5), P. 769 - 788
Published: Feb. 20, 2022
Abstract
The
ongoing
COVID‐19
pandemic
caused
by
SARS‐CoV‐2
is
associated
with
high
morbidity
and
mortality.
This
zoonotic
virus
has
emerged
in
Wuhan
of
China
December
2019
from
bats
pangolins
probably
continuing
the
human‐to‐human
transmission
globally
since
last
two
years.
As
there
no
efficient
approved
treatment,
a
number
vaccines
were
developed
at
an
unprecedented
speed
to
counter
pandemic.
Moreover,
vaccine
hesitancy
observed
that
may
be
another
possible
reason
for
this
never
ending
In
meantime,
several
variants
mutations
identified
causing
multiple
waves
globally.
Now
safety
efficacy
these
are
debatable
recommended
determine
whether
able
interrupt
variant
concern
(VOC).
VOCs
continue
emerge
appear
more
transmissible
less
sensitive
virus‐specific
immune
responses.
overview,
we
have
highlighted
various
drugs
used
along
their
reported
side
effects.
preliminary
data
novel
VOC
“Omicron”
discussed
existing
animal
models.
Science Translational Medicine,
Journal Year:
2022,
Volume and Issue:
14(658)
Published: Aug. 17, 2022
Despite
the
remarkable
efficacy
of
COVID-19
vaccines,
waning
immunity
and
emergence
SARS-CoV-2
variants
such
as
Omicron
represents
a
global
health
challenge.
Here,
we
present
data
from
study
in
nonhuman
primates
demonstrating
durable
protection
against
BA.1
variant
induced
by
subunit
vaccine
comprising
receptor
binding
domain
ancestral
strain
(RBD-Wu)
on
I53-50
nanoparticle
adjuvanted
with
AS03,
which
was
recently
authorized
for
use
individuals
18
years
or
older.
Vaccination
neutralizing
antibody
(nAb)
titers
that
were
maintained
at
high
concentrations
least
1
year
after
two
doses,
pseudovirus
nAb
geometric
mean
titer
(GMT)
1978
live
virus
GMT
1331
but
not
variant.
However,
booster
dose
6
to
12
months
RBD-Wu
RBD-β
(RBD
Beta
variant)
displayed
elicited
variants.
In
addition,
observed
persistent
neutralization
panel
sarbecoviruses,
including
SARS-CoV.
Furthermore,
there
substantial
memory
T
B
cell
responses
reactive
resulted
infection
lung
suppression
viral
burden
nares
weeks
final
immunization.
Even
vaccination,
rapid
control
nares.
These
results
highlight
cross-protective
AS03-adjuvanted
RBD-I53-50
vaccine.
ChemBioChem,
Journal Year:
2022,
Volume and Issue:
23(9)
Published: March 23, 2022
The
SARS-CoV-2
virus
has
shown
increased
ability
to
mutate
over
the
past
two
years,
especially
in
regions
of
spike
protein
and
receptor
binding
sites.
Omicron
(B.1.1.529)
is
fifth
variant
concern
(VOC)
after
emergence
Alpha,
Beta,
Gamma,
Delta
VOCs
SARS-CoV-2.
This
new
now
circulated
128
countries
according
Global
Initiative
on
Sharing
All
Influenza
Data
(GISAID),
these
have
shared
650,657
genome
sequences
as
26
January,
2022.
In
this
article,
we
highlight
real
challenges
its
different
lineages.
Nature Communications,
Journal Year:
2022,
Volume and Issue:
13(1)
Published: July 30, 2022
Studies
are
needed
to
evaluate
the
safety
and
effectiveness
of
mRNA
SARS-CoV-2
vaccination
during
pregnancy,
levels
protection
provided
their
newborns
through
placental
transfer
antibodies.
Here,
we
transplacental
vaccine
products
functional
anti-SARS-CoV-2
antibodies
pregnancy
early
infancy
in
a
cohort
20
individuals
vaccinated
late
pregnancy.
We
find
no
evidence
maternal
blood,
placenta
tissue,
or
cord
blood
at
delivery.
However,
time-dependent
efficient
IgG
neutralizing
neonate
that
persists
infancy.
Additionally,
using
phage
immunoprecipitation
sequencing,
vaccine-specific
signature
Spike
protein
epitope
binding
is
transplacentally
transferred
Timing
critical
ensure
protective