iScience,
Journal Year:
2024,
Volume and Issue:
27(8), P. 110470 - 110470
Published: July 8, 2024
Besides
neutralizing
antibodies,
which
are
considered
an
important
measure
for
vaccine
immunogenicity,
Fc-mediated
antibody
functions
can
contribute
to
antibody-mediated
protection.
They
strongly
influenced
by
structural
properties
such
as
subclass
and
Fc
glycan
composition.
We
here
applied
a
systems
serology
approach
dissect
humoral
immune
responses
induced
MVA-MERS-S,
MVA-vectored
against
the
Middle
East
respiratory
syndrome
coronavirus
(MERS-CoV).
Building
on
preceding
studies
reporting
safety
immunogenicity
of
our
study
highlights
potential
late
boost,
administered
one
year
after
prime,
enhance
both
functionality
compared
primary
vaccination
series.
Distinct
characteristics
were
observed
antibodies
specific
MERS-CoV
spike
protein
S1
S2
subunits,
regarding
compositions
well
functionality.
These
findings
highlight
benefit
homologous
booster
with
MVA-MERS-S
may
be
interest
design
future
vaccines.
Biosensors,
Journal Year:
2024,
Volume and Issue:
14(3), P. 146 - 146
Published: March 15, 2024
The
global
challenges
posed
by
the
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
pandemic
have
underscored
critical
importance
of
innovative
and
efficient
control
systems
for
addressing
future
pandemics.
most
effective
way
to
is
rapidly
suppress
spread
virus
through
early
detection
using
a
rapid,
accurate,
easy-to-use
diagnostic
platform.
In
biosensors
that
use
bioprobes,
binding
affinity
molecular
recognition
elements
(MREs)
primary
factor
determining
dynamic
range
sensing
Furthermore,
sensitivity
relies
mainly
on
bioprobe
quality
with
sufficient
functionality.
This
comprehensive
review
investigates
aptamers
nanobodies
recently
developed
as
advanced
MREs
SARS-CoV-2
therapeutic
applications.
These
bioprobes
might
be
integrated
into
organic
bioelectronic
materials
devices,
promising
enhanced
specificity.
offers
valuable
insights
advancing
biosensing
technologies
infectious
disease
diagnosis
treatment
new
bioprobes.
Currently,
SARS-CoV-2
has
evolved
into
various
variants,
including
the
numerous
highly
mutated
Omicron
sub-lineages,
significantly
increasing
immune
evasion
ability.
The
development
raises
concerns
about
possibly
diminished
effectiveness
of
available
vaccines
and
antibody-based
therapeutics.
Here,
we
describe
those
representative
categories
broadly
neutralizing
antibodies
(bnAbs)
that
retain
prominent
against
emerging
variants
sub-lineages.
molecular
characteristics,
epitope
conservation,
resistance
mechanisms
these
are
further
detailed,
aiming
to
offer
suggestion
or
direction
for
therapeutic
antibodies,
facilitate
vaccine
design
with
broad-spectrum
potential.
Vaccines,
Journal Year:
2023,
Volume and Issue:
11(11), P. 1644 - 1644
Published: Oct. 26, 2023
Herein,
we
review
established
clinical
use
cases
for
SARS-CoV-2
antibody
measures,
which
include
diagnosis
of
recent
prior
infection,
isolating
high
titer
convalescent
plasma,
diagnosing
multisystem
inflammatory
syndrome
in
children
(MIS-C),
and
booster
dosing
the
immunosuppressed
other
populations.
We
then
address
whether
an
correlate
protection
(CoP)
has
been
successfully
defined
with
following
considerations:
Antibody
responses
immunocompetent,
vaccine
type,
variants,
binding
tests
vs.
neutralization
tests,
endpoint
measures.
In
transition
from
COVID-19
pandemic
to
endemic,
there
much
interest
defining
CoP.
Due
mutability
respiratory
viruses
our
current
knowledge
variants
a
CoP
prevention
infection
is
unrealistic.
However,
may
be
severe
disease
requiring
hospitalization
and/or
death.
Most
research
focused
on
measurements.
can
significant
differences
test
methods,
disparate
new
depending
format.
Furthermore,
assays
are
often
impractical
throughput
applications
(e.g.,
assessing
humoral
immune
response
populations
or
large
cohorts).
Nevertheless,
studies
using
measures
reviewed
determine
where
consensus.
Alternatively,
could
used
define
Binding
tend
highly
automatable,
throughput,
therefore
practical
population
applications.
Again,
consensus
vaccines,
focusing
standardized
results.
antibodies
directed
against
S1
receptor
domain
(S1-RBD)
viral
spike
protein
provide
practical,
indirect
measure
neutralization.
Initially,
S1-RBD
selected
that
reflects
peak
immunocompetent
serve
as
target
immunocompromised.
From
existing
reporting
units,
approximate
range
1372–2744
BAU/mL
mRNA
recombinant
vaccines
was
extracted
initial
target.
This
would
need
confirmed
potentially
adjusted
updated
almost
certainly
formats
(i.e.,
vector).
threshold
based
outcomes
over
time
disease).
also
discuss
precedent
measurement
vaccine-preventable
diseases
hepatitis
B).
Lastly,
cellular
immunity
briefly
addressed
its
importance
nature
durability
protection.
iScience,
Journal Year:
2024,
Volume and Issue:
27(4), P. 109363 - 109363
Published: Feb. 29, 2024
Highlights•Anti-SARS-CoV-2
bispecific
Abs
can
be
generated
by
combining
non-neutralizing
Abs•Anti-S2
antibody
CvMab-62
recognizes
a
novel
epitope
upstream
of
S2
stem
helix•Bispecific
antibodies
inhibit
spike-mediated
membrane
fusogenic
mechanism•Bispecific
restore
antiviral
activity
against
bebtelovimab-resistant
BQ.1.1SummaryA
current
challenge
is
the
emergence
SARS-CoV-2
variants,
such
as
BQ.1.1
and
XBB.1.5,
that
evade
immune
defenses,
thereby
limiting
drug
effectiveness.
Emergency-use
drugs,
including
widely
effective
bebtelovimab,
are
losing
their
benefits.
One
potential
approach
to
address
this
issue
which
combine
targeting
abilities
two
with
distinct
epitopes.
We
engineered
neutralizing
in
IgG-scFv
format
from
initially
antibodies,
CvMab-6
(which
binds
receptor-binding
domain
[RBD])
(targeting
spike
protein
subunit
adjacent
known
anti-S2
epitope).
Furthermore,
we
created
incorporating
scFv
bebtelovimab
our
antibody,
demonstrating
significant
restoration
effectiveness
variants.
This
study
highlights
existing
less
anti-RBD
revive
therapeutics
compromised
immune-evading
variants.Graphical
abstract
Biological and Pharmaceutical Bulletin,
Journal Year:
2024,
Volume and Issue:
47(5), P. 917 - 923
Published: April 30, 2024
The
global
coronavirus
disease
2019
(COVID-19)
pandemic,
caused
by
severe
acute
respiratory
syndrome
2
(SARS-CoV-2),
has
devastated
public
health
and
the
economy.
New
variants
are
continually
emerging
because
of
amino
acid
mutations
within
SARS-CoV-2
spike
protein.
Existing
neutralizing
antibodies
(nAbs)
that
target
receptor-binding
domain
(RBD)
protein
have
been
shown
to
reduced
activity
against
these
variants.
In
particular,
recently
expanding
omicron
subvariants
BQ
1.1
XBB
resistant
nAbs
approved
for
emergency
use
United
States
Food
Drug
Administration.
Therefore,
it
is
essential
develop
broad
combat
contrast
massive
accumulation
RBD,
S2
subunit
remains
highly
conserved
among
targeting
region
may
provide
effective
cross-protection
novel
Here,
we
a
detailed
summary
subunit:
fusion
peptide,
stem
helix,
heptad
repeats
1
2.
addition,
prospects
solve
problems
such
as
weak
potency
subunit.
Viruses,
Journal Year:
2024,
Volume and Issue:
16(6), P. 900 - 900
Published: June 1, 2024
Currently,
SARS-CoV-2
has
evolved
into
various
variants,
including
the
numerous
highly
mutated
Omicron
sub-lineages,
significantly
increasing
immune
evasion
ability.
The
development
raises
concerns
about
possibly
diminished
effectiveness
of
available
vaccines
and
antibody-based
therapeutics.
Here,
we
describe
those
representative
categories
broadly
neutralizing
antibodies
(bnAbs)
that
retain
prominent
against
emerging
variants
sub-lineages.
molecular
characteristics,
epitope
conservation,
resistance
mechanisms
these
are
further
detailed,
aiming
to
offer
suggestion
or
direction
for
therapeutic
antibodies,
facilitate
design
with
broad-spectrum
potential.
PLoS Pathogens,
Journal Year:
2024,
Volume and Issue:
20(8), P. e1012383 - e1012383
Published: Aug. 2, 2024
The
SARS-CoV-2
virus
responsible
for
the
COVID-19
global
pandemic
has
exhibited
a
striking
capacity
viral
evolution
that
drives
continued
evasion
from
vaccine
and
infection-induced
immune
responses.
Mutations
in
receptor
binding
domain
of
S1
subunit
spike
glycoprotein
have
led
to
considerable
escape
antibody
responses,
reducing
efficacy
vaccines
monoclonal
(mAb)
therapies.
Therefore,
there
is
need
interrogate
more
constrained
regions
spike,
such
as
S2
subdomain.
Here,
we
present
collection
mAbs
two
convalescent
individuals
target
multiple
S2,
including
outside
those
commonly
reported.
One
mAbs,
C20.119,
which
bound
highly
conserved
epitope
fusion
peptide,
was
able
broadly
neutralize
across
variants,
SARS-CoV-1,
closely
related
zoonotic
sarbecoviruses.
majority
were
non-neutralizing;
however,
many
them
could
mediate
antibody-dependent
cellular
cytotoxicity
(ADCC)
at
levels
similar
S1-targeting
mAb
S309
previously
authorized
treatment
infections.
Several
with
ADCC
function
also
trimers
other
human
coronaviruses
(HCoVs),
MERS-CoV
HCoV-HKU1.
Our
findings
suggest
can
diverse
epitopes
functional
HCoV
sarbecovirus
breadth
likely
functionally
spike.
These
be
developed
potential
future
pandemics,
while
providing
insight
into
ideal
eliciting
broad
response.
Epidemiology and Vaccinal Prevention,
Journal Year:
2025,
Volume and Issue:
23(6), P. 169 - 176
Published: Jan. 15, 2025
Relevance
.
COVID-19,
caused
by
the
SARS-CoV-2
virus,
remains
a
global
public
health
threat
despite
end
of
pandemic.
In
four
years
since
onset
pandemic,
genome
has
undergone
significant
changes,
particularly
in
gene
encoding
spike
(S)
protein.
These
changes
resulted
from
accumulation
immune
responses
human
population,
allowing
virus
to
evade
response.
A
proportion
population
was
infected
early
pandemic
or
vaccinated
with
vaccines
based
on
earlier
variants
virus.
The
emergence
new
mutant
raises
concerns
about
potential
for
severe
COVID-19
previously
individuals.
Аim
To
examine
specifics
antibody
formation,
as
well
spectrum
and
functional
activity
these
antibodies
patients
COVID-19.
Conclusion
s.
Antibodies
produced
response
infection
vaccination
show
diversity
activity.
Changes
viral
may
reduce
effectiveness,
highlighting
importance
monitoring
developing
adapted
vaccines.
data
will
be
key
shaping
treatment
strategies
changing
epidemiological
situation.