Kinetics of specific anti-SARS-CoV-2 IgM, IgA, and IgG responses during the first 12 months after SARS-CoV-2 infection: A prospective longitudinal study
PLoS ONE,
Journal Year:
2023,
Volume and Issue:
18(7), P. e0288557 - e0288557
Published: July 12, 2023
Coronavirus
2019
(COVID-19)
is
a
global
health
threat.
The
kinetics
of
antibodies
against
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
need
to
be
assessed,
as
the
long-term
duration
these
immunoglobulins
remains
largely
controversial.
aim
this
study
was
assess
longitudinal
dynamics
anti-SARS-CoV-2
nucleocapsid
(N)
protein
and
receptor-binding
domain
(RBD)
spike
up
one
year
in
cohort
190
COVID-19
patients.
Between
March
September
2021,
we
enrolled
patients
from
two
regional
hospitals
Casablanca,
Morocco.
Blood
samples
were
collected
analyzed
for
antibody
levels.
We
used
commercial
Euroimmun
ELISA
determination
anti-N
IgM,
Abbott
Architect
™
SARS-CoV-2
IgG
test
detection
anti-RBD
IgG,
an
in-house
kit
assay
IgA.
IgM
IgA
assessed
2–5,
9–12,
17–20
32–37
days
after
symptom
onset.
also
60,
90,
120
360
One-third
developed
(32%),
while
two-thirds
(61%).
One
month
onset,
most
with
97%
93%
positivity
respectively.
rate
remained
high
follow-up.
However,
decreased
over
time,
only
41%
testing
positive
year’s
levels
significantly
higher
older
people
(over
50
years)
than
other
participants.
found
that
who
had
received
doses
ChAdOx1
nCoV-19
vaccine
prior
infection
lower
response
unvaccinated
This
difference
statistically
significant
weeks
onset
symptoms.
present
first
Africa
measure
(IgA,
IgG)
year.
Most
participants
seropositive
but
showed
decline
titers.
Language: Английский
High-resolution kinetics and cellular determinants of antibody response to SARS-CoV-2 over two years after COVID-19 vaccination
Research Square (Research Square),
Journal Year:
2024,
Volume and Issue:
unknown
Published: Jan. 17, 2024
Abstract
Despite
widespread
COVID-19
vaccine
coverage,
breakthrough
infections
are
increasing,
mainly
driven
by
waning
immunity
and
the
emergence
of
SARS-CoV-2
Omicron
variants.
Here,
we
characterized
IgM,
IgA
IgG
kinetics
in
55
visits
over
two
years
post-COVID-19
vaccination,
T-cell
responses
six
months
post-booster,
31
healthy
adults.
Antibodies
to
Wuhan
antigens
Alpha,
Delta
variants
were
quantified
Luminex.
SARS-CoV-2-specific
measured
activation-induced
marker
(AIM)
IFN-γ/IL-2
FluoroSpot
assays.
Antibody
trajectories
varied
among
isotypes.
decayed
slowly
during
first
subsequently
slowed
down.
exhibited
a
rapid
initial
decay
rate
that
decelerated
stabilizing
above
seropositivity
threshold.
Contrarily,
IgM
rapidly
dropped
undetectable
levels
after
primary
vaccination.
Importantly,
three
doses
induced
higher
more
persistent
anti-spike
(S)
compared
doses,
whereas
infection
led
superior
longer-lasting
anti-S
or
doses.
subvariants
had
shorter
persistence
than
ancestral
virus.
Finally,
polyfunctional
T
cells
correlated
positively
with
subsequent
responses.
These
results
revealed
distinct
isotype
non-constant
highlighted
benefits
booster
enhancing
sustaining
antibody
Language: Английский
High-resolution kinetics and cellular determinants of SARS-CoV-2 antibody response over two years after COVID-19 vaccination
Microbes and Infection,
Journal Year:
2024,
Volume and Issue:
unknown, P. 105423 - 105423
Published: Sept. 1, 2024
Severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
studies
usually
rely
on
cross-sectional
data
of
large
cohorts
but
limited
repeated
samples,
overlooking
significant
inter-individual
antibody
kinetic
differences.
By
combining
Luminex,
activation-induced
marker
(AIM)
and
IFN-γ/IL-2
Fluorospot
assays,
we
characterized
the
IgM,
IgA,
IgG
kinetics
using
610
samples
from
31
healthy
adults
over
two
years
after
COVID-19
vaccination,
T-cell
responses
six
months
post-booster.
Antibody
trajectories
varied
among
isotypes:
decayed
slowly,
IgA
exhibited
an
initial
sharp
decline,
which
gradually
slowed
down
stabilized
above
seropositivity
threshold.
Contrarily,
IgM
rapidly
dropped
to
undetectable
levels
primary
vaccination.
Importantly,
three
vaccine
doses
induced
higher
more
durable
anti-spike
compared
doses,
whereas
infection
led
highest
peak
slowest
decay
rate
Comparing
with
ancestral
virus,
recognizing
Omicron
subvariants
had
a
faster
decay.
Finally,
polyfunctional
T
cells
were
positively
associated
subsequent
responses.
These
results
revealed
distinctive
patterns
by
isotype
highlight
benefits
booster
in
enhancing
sustaining
Language: Английский
Comparable and sustained levels of S1-RBD-IgG and S1-RBD-IgA in BNT162b2 homologous and CoronaVac-BNT162b2 heterologous booster vaccination: A 22-month prospective study in Malaysia
Vaccine,
Journal Year:
2024,
Volume and Issue:
42(26), P. 126471 - 126471
Published: Oct. 28, 2024
Language: Английский
Induction of Fc-dependent functional antibodies against different variants of SARS-CoV-2 varies by vaccine type and prior infection
Alexander W. Harris,
No information about this author
Liriye Kurtovic,
No information about this author
Jeane Nogueira
No information about this author
et al.
Communications Medicine,
Journal Year:
2024,
Volume and Issue:
4(1)
Published: Dec. 19, 2024
SARS-CoV-2
transmission
and
COVID-19
disease
severity
is
influenced
by
immunity
from
natural
infection
and/or
vaccination.
Population-level
complicated
the
emergence
of
viral
variants.
Antibody
Fc-dependent
effector
functions
are
as
important
mediators
in
immunity.
However,
their
induction
populations
with
diverse
vaccination
histories
against
variants
remains
poorly
defined.
We
evaluated
functional
antibodies
following
two
widely
used
vaccines,
AstraZeneca
(AZ)
Sinovac
(SV),
including
antibody
binding
Fcγ-receptors
complement-fixation
vaccinated
Brazilian
adults
(n
=
222),
some
who
were
previously
infected
SARS-CoV-2,
well
only
200).
IgG,
IgM,
IgA,
IgG
subclasses
also
quantified.
AZ
induces
greater
Fcγ-receptor-binding
(types
I,
IIa,
IIIa/b)
than
SV
or
infection.
Previously
individuals
have
significantly
vaccine-induced
responses
compared
to
naïve
counterparts.
highest
among
a
prior
infection,
for
all
receptor
types,
substantial
complement-fixing
activity
seen
this
group.
higher
IgM
AZ,
but
does
not
drive
better
activity.
Some
associated
subject
age,
whereas
not.
Importantly,
retained
Omicron
BA.1
S
protein,
being
best
Fcγ-receptor-1
binding,
SV.
Hybrid
immunity,
combined
exposure
vaccination,
generates
strong
Fc-mediated
which
may
contribute
evolving
Understanding
determinants
enable
future
vaccines
efficacy
different
Antibodies
proteins
produced
part
immune
response
that
identify
prevent
negative
consequences
infections.
studied
adults,
whom
had
COVID-19.
Differences
produced,
more
active
people
There
differences
how
effective
This
improved
understanding
could
inform
development
improve
impact
Harris
et
al.
evaluate
COVID
adults.
Vaccine
underlie
observed
IIIa/b),
IgA
production,
antibodies.
Language: Английский
IGG and IGM response in a group of Iraqi health care worker following SARS-CoV-2 mRNA vaccine
Amar Kasim Muhamad,
No information about this author
Russell Abo-Altemen,
No information about this author
Amar Muhamad
No information about this author
et al.
Journal of Population Therapeutics and Clinical Pharmacology,
Journal Year:
2023,
Volume and Issue:
30(6)
Published: Jan. 1, 2023
The
global
pandemic
of
coronavirus
disease
2019
(COVID-19)
is
caused
by
infection
with
the
SARS-CoV-2
virus.Positive
detection
IgM
and
IgG
antibodies
specific
to
has
been
recognized
as
an
evidence
for
confirmed
or
vaccination.Method:
One
hundred
healthy
health
care
workers
from
both
genders
over
eighteen
years
old
were
participated
test
their
humeral
response
(IgG,
IgM)
after
vaccinated
Pfizer
vaccine
in
vaccination
center
Baghdad
Teaching
Hospital
one
week
second
shot,
matched
age
gender
had
before
they
get
(control),
groups
deny
recent
COVID-19
infection.Result:
Our
finding
shows
that
increase
antibody
responses
following
lesser
extent
titer
than
obvious
our
entire
participant
compared
control.Conclusion
result
support
successful
production
humoral
immunity
protection
against
infection.
Language: Английский
Fc-dependent functional activity of ChAdOx1-S and CoronaVac vaccine-induced antibodies to the SARS-CoV-2 spike protein
Alexander W. Harris,
No information about this author
Liriye Kurtovic,
No information about this author
Jeane Nogueira
No information about this author
et al.
medRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2023,
Volume and Issue:
unknown
Published: Oct. 25, 2023
Abstract
Ongoing
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
transmission
and
COVID-19
disease
severity
is
influenced
by
immunity
acquired
natural
exposure
and/or
vaccination,
whereby
most
vaccines
are
formulated
on
the
Ancestral
strain.
However,
population-level
complicated
emergence
of
variants
concern
(VOCs),
such
as
Omicron
that
dominant
variant
currently
in
circulation.
Antibody
Fc-dependent
effector
functions
being
increasingly
recognised
important
mediators
immunity,
especially
against
VOCs.
induction
these
populations
with
diverse
infection
vaccination
histories,
remains
poorly
defined.
Here,
we
evaluated
functional
antibodies
following
two
widely
used
vaccines:
AstraZeneca
(AZ;
ChAdOx1-S)
Sinovac
(SV).
We
quantified
FcγR-binding
C1q-fixing
spike
(S)
proteins
Brazilian
adults
vaccinated
AZ
or
SV
(n=222),
some
which
were
previously
exposed
to
SARS-CoV-2.
induced
greater
responses
S
than
vaccine.
Previously
individuals
had
significantly
vaccine-induced
compared
their
naïve
counterparts,
notably
high
C1q-fixation
levels,
irrespective
vaccine
type.
was
highest
among
a
prior
exposure,
well
retained
protein.
Overall,
findings
contribute
our
understanding
its
effectiveness
evolving
variants.
Language: Английский