Microorganisms,
Год журнала:
2023,
Номер
11(9), С. 2347 - 2347
Опубликована: Сен. 20, 2023
Since
the
onset
of
COVID-19
pandemic,
humanity
has
experienced
spread
and
circulation
several
SARS-CoV-2
variants
that
differed
in
transmissibility,
contagiousness,
ability
to
escape
from
vaccine-induced
neutralizing
antibodies.
However,
issues
related
differences
variant-specific
immune
responses
remain
insufficiently
studied.
The
aim
this
study
was
compare
parameters
humoral
two
groups
patients
with
acute
who
were
infected
during
period
D614G
Delta
SARS-CoV-2.
Sera
48
tested
for
binding
antibodies
using
six
assays.
We
found
serum
samples
demonstrated
3.9-
1.6-fold
increases
RBD-
spike-specific
IgG
wild-type
antigens
compared
variant
(p
<
0.01).
Cluster
analysis
showed
existence
well-separated
clusters.
first
cluster
mainly
consisted
D614G-period
second
predominantly
included
period.
results
thus
obtained
indicate
D614G-
Delta-specific
infections
can
be
characterized
by
signatures.
This
taken
into
account
when
developing
new
vaccines.
Cell Reports,
Год журнала:
2024,
Номер
43(9), С. 114684 - 114684
Опубликована: Авг. 30, 2024
Immunity
acquired
by
vaccination
following
infection,
termed
hybrid
immunity,
has
been
shown
to
confer
enhanced
protection
against
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
enhancing
the
breadth
and
potency
of
immune
responses.
Here,
we
assess
Fc-mediated
humoral
profiles
in
immunity
their
association
with
age
vaccine
type.
Participants
are
divided
into
three
groups:
infection
only,
(i.e.,
immunity).
Using
systems
serology,
profile
responses
spikes
subdomains
SARS-CoV-2
variants.
We
find
that
is
characterized
superior
Fc
receptor
binding
natural
killer
(NK)
cell-,
neutrophil-,
complement-activating
antibodies,
which
higher
than
what
can
be
expected
from
sum
infection.
These
differences
between
vaccine-induced
more
pronounced
aged
adults,
especially
for
immunoglobulin
(Ig)G1,
IgG2,
Fcγ
receptor-binding
antibodies.
Our
findings
suggest
strategies
aim
mimic
should
consider
as
an
important
modifier.
Vaccines,
Год журнала:
2024,
Номер
12(10), С. 1089 - 1089
Опубликована: Сен. 24, 2024
Correlates
of
Protection
(CoP)
are
biomarkers
above
a
defined
threshold
that
can
replace
clinical
outcomes
as
primary
endpoints,
predicting
vaccine
effectiveness
to
support
the
approval
new
vaccines
or
follow
up
studies.
In
context
COVID-19
vaccination,
CoPs
help
address
challenges
such
demonstrating
in
special
populations,
against
emerging
SARS-CoV-2
variants
determining
durability
vaccine-elicited
immunity.
While
anti-spike
IgG
titres
and
viral
neutralising
capacity
have
been
characterised
for
contribution
other
components
humoral
immune
response
immediate
long-term
protective
immunity
is
less
well
characterised.
This
review
examines
evidence
supporting
use
trials,
how
they
be
used
define
It
also
highlights
alternative
biomarkers,
including
Fc
effector
function,
mucosal
immunity,
generation
long-lived
plasma
memory
B
cells
discuss
these
applied
studies
tools
available
study
them.
Vaccines,
Год журнала:
2024,
Номер
12(10), С. 1123 - 1123
Опубликована: Сен. 30, 2024
Approximately
10-20%
of
subjects
vaccinated
with
HBsAg-based
hepatitis
B
virus
(HBV)
vaccines
are
non-responders.
BM32
is
a
recombinant
grass
pollen
allergy
vaccine
containing
the
HBV-derived
preS
surface
antigen
as
an
immunological
carrier
protein.
PreS
includes
binding
site
HBV
to
its
receptor
on
hepatocytes.
We
investigated
whether
non-responsiveness
after
repeated
vaccinations
could
be
overcome
by
immunization
VVX001
(i.e.,
alum-adsorbed
BM325,
component
BM32).
medRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2024,
Номер
unknown
Опубликована: Окт. 18, 2024
Abstract
SARS-CoV-2
vaccine-acquired
immunity
provides
robust
cross-variant
recognition,
while
infection-acquired
can
be
heterogenous,
with
disease
severity
often
modulating
post-recovery
responses.
We
assessed
antibody
waning
dynamics
between
infection-
and
vaccination-acquired
across
variants
of
concern
(VOC).
mRNA
vaccination
induced
potent,
cross-VOC
Spike
recognition
functional
responses,
but
waned
more
rapidly
for
Omicron
Spike.
Hospitalized
individuals
developed
durable
responses
lower
peaks
compared
to
vaccination,
outpatients
exhibited
slower
decay
than
inactivated
vaccine
recipients.
Humoral
the
receptor
binding
domain
tracked
neutralizing
titers,
S2-directed
antibody-dependent
myeloid
cellular
phagocytosis.
Boosting
recovered
patients
or
vaccines
expanded
humoral
breadth,
durability,
restored
eliminating
severity-
platform-associated
differences.
Therefore,
hybrid
immunization
compensates
this
distinction
broadens
highlighting
value
boosting
in
previously
infected
individuals.
One
Sentence
Summary
Infection-
COVID-19
exhibit
different
profiles,
each
characterized
by
distinct
kinetics
over
time.
Since
the
onset
of
COVID‐19
pandemic,
humanity
has
experienced
spread
and
circulation
several
SARS-CoV-2
variants
that
differed
in
transmissibility,
contagiousness,
ability
to
escape
from
vaccine-induced
neutralizing
antibodies.
However,
issues
related
differences
variant-specific
immune
responses,
remain
insufficiently
studied.
The
aim
this
study
was
compare
parameters
humoral
responses
two
groups
patients
with
acute
COVID-19
who
were
infected
during
period
D614G
Delta
SARS-CoV-2.
Sera
48
tested
for
binding
antibodies
using
six
assays.
We
found
serum
samples
demonstrated
3.9‐
1.6‐fold
increase
RBD-
Spike‐specific
IgG
Wild
type
antigens
compared
variant
(p
&lt;
0.01).
Cluster
analysis
showed
existence
well-separated
clusters.
first
cluster
mainly
consisted
second
predominantly
included
period.
results
thus
obtained
indicate
D614G-
Delta-specific
infections
can
be
characterized
by
signatures.
This
taken
into
account
when
developing
new
vaccines.
Microorganisms,
Год журнала:
2023,
Номер
11(9), С. 2347 - 2347
Опубликована: Сен. 20, 2023
Since
the
onset
of
COVID-19
pandemic,
humanity
has
experienced
spread
and
circulation
several
SARS-CoV-2
variants
that
differed
in
transmissibility,
contagiousness,
ability
to
escape
from
vaccine-induced
neutralizing
antibodies.
However,
issues
related
differences
variant-specific
immune
responses
remain
insufficiently
studied.
The
aim
this
study
was
compare
parameters
humoral
two
groups
patients
with
acute
who
were
infected
during
period
D614G
Delta
SARS-CoV-2.
Sera
48
tested
for
binding
antibodies
using
six
assays.
We
found
serum
samples
demonstrated
3.9-
1.6-fold
increases
RBD-
spike-specific
IgG
wild-type
antigens
compared
variant
(p
<
0.01).
Cluster
analysis
showed
existence
well-separated
clusters.
first
cluster
mainly
consisted
D614G-period
second
predominantly
included
period.
results
thus
obtained
indicate
D614G-
Delta-specific
infections
can
be
characterized
by
signatures.
This
taken
into
account
when
developing
new
vaccines.