Science Translational Medicine,
Journal Year:
2022,
Volume and Issue:
14(634)
Published: Jan. 14, 2022
Multiple
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
variants
that
have
mutations
associated
with
increased
transmission
and
antibody
escape
arisen
over
the
course
of
current
pandemic.
Although
vaccines
largely
been
effective
against
past
variants,
number
found
on
Omicron
(B.1.1.529)
spike
protein
appear
to
diminish
protection
conferred
by
preexisting
immunity.
Using
vesicular
stomatitis
virus
(VSV)
pseudoparticles
expressing
several
SARS-CoV-2
we
evaluated
magnitude
breadth
neutralizing
response
time
in
individuals
after
infection
mRNA-vaccinated
individuals.
We
observed
boosting
increases
wild-type
(D614),
Beta,
Delta,
variants;
however,
variant
was
most
resistant
neutralization.
further
vaccinated
healthy
adults
had
robust
broad
responses,
whereas
responses
may
reduced
pregnant
women,
underscoring
importance
learning
how
maximize
mRNA
vaccine
populations.
Findings
from
this
study
show
substantial
heterogeneity
vaccination
support
addition
more
conserved
viral
antigens
existing
vaccines.
Journal of Clinical Investigation,
Journal Year:
2021,
Volume and Issue:
131(17)
Published: Aug. 31, 2021
Defining
the
correlates
of
protection
necessary
to
manage
COVID-19
pandemic
requires
analysis
both
antibody
and
T
cell
parameters,
but
complexity
traditional
tests
limits
virus-specific
measurements.
We
tested
sensitivity
performance
a
simple
rapid
SARS-CoV-2
spike
protein–specific
test
based
on
stimulation
whole
blood
with
peptides
covering
protein,
followed
by
cytokine
(IFN-γ,
IL-2)
measurement
in
different
cohorts
including
BNT162b2-vaccinated
individuals
(n
=
112),
convalescent
asymptomatic
symptomatic
patients
130),
SARS-CoV-1–convalescent
12).
The
this
is
comparable
that
methods
(ELISPOT,
activation-induced
marker).
Using
test,
we
observed
similar
mean
magnitude
responses
between
vaccinees
convalescents
3
months
after
vaccination
or
virus
priming.
However,
wide
heterogeneity
spike-specific
characterized
individual
responses,
irrespective
time
analysis.
these
cannot
be
predicted
from
neutralizing
levels.
Hence,
humoral
cellular
spike–specific
immunity
should
define
evaluate
current
vaccine
strategies.
Clinical Infectious Diseases,
Journal Year:
2021,
Volume and Issue:
75(1), P. e1037 - e1045
Published: Nov. 15, 2021
Abstract
Background
Patients
treated
with
anti-CD20
therapy
are
particularly
at
risk
of
developing
severe
coronavirus
disease
2019
(COVID-19);
however,
little
is
known
regarding
COVID-19
vaccine
effectiveness
in
this
population.
Methods
This
prospective
observational
cohort
study
assesses
humoral
and
T-cell
responses
after
vaccination
2
doses
mRNA-based
vaccines
patients
rituximab
for
rheumatic
diseases
or
ocrelizumab
multiple
sclerosis
(n
=
37),
compared
to
immunocompetent
individuals
22).
Results
Severe
acute
respiratory
syndrome
(SARS-CoV-2)-specific
antibodies
were
detectable
only
69.4%
levels
that
significantly
lower
controls
who
all
seroconverted.
In
contrast
antibodies,
Spike
(S)-specific
CD4
T
cells
equally
detected
(85–90%)
mostly
a
Th1
phenotype.
Response
rates
S-specific
CD8
higher
(96.2%)
rituximab-treated
(81.8%)
as
(66.7%).
polyfunctional
but
expressed
more
effector
molecules
than
controls.
During
follow-up,
3
MS
without
SARS-CoV-2-specific
antibody
response
had
mild
breakthrough
infection.
One
them
no
vaccination.
Conclusions
Our
suggests
on
treatment
able
mount
potent
mRNA
vaccines,
despite
impaired
responses.
could
play
an
important
role
the
reduction
complications
COVID-19.
Science Translational Medicine,
Journal Year:
2022,
Volume and Issue:
14(634)
Published: Jan. 14, 2022
Multiple
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
variants
that
have
mutations
associated
with
increased
transmission
and
antibody
escape
arisen
over
the
course
of
current
pandemic.
Although
vaccines
largely
been
effective
against
past
variants,
number
found
on
Omicron
(B.1.1.529)
spike
protein
appear
to
diminish
protection
conferred
by
preexisting
immunity.
Using
vesicular
stomatitis
virus
(VSV)
pseudoparticles
expressing
several
SARS-CoV-2
we
evaluated
magnitude
breadth
neutralizing
response
time
in
individuals
after
infection
mRNA-vaccinated
individuals.
We
observed
boosting
increases
wild-type
(D614),
Beta,
Delta,
variants;
however,
variant
was
most
resistant
neutralization.
further
vaccinated
healthy
adults
had
robust
broad
responses,
whereas
responses
may
reduced
pregnant
women,
underscoring
importance
learning
how
maximize
mRNA
vaccine
populations.
Findings
from
this
study
show
substantial
heterogeneity
vaccination
support
addition
more
conserved
viral
antigens
existing
vaccines.