Science Translational Medicine,
Journal Year:
2022,
Volume and Issue:
14(636)
Published: Feb. 1, 2022
Transplant
recipients,
who
receive
therapeutic
immunosuppression
to
prevent
graft
rejection,
are
characterized
by
high
coronavirus
disease
2019
(COVID-19)-related
mortality
and
defective
response
vaccines.
We
observed
that
previous
infection
with
severe
acute
respiratory
syndrome
2
(SARS-CoV-2),
but
not
the
standard
two-dose
regimen
of
vaccination,
provided
protection
against
symptomatic
COVID-19
in
kidney
transplant
recipients.
therefore
compared
cellular
humoral
immune
responses
these
two
groups
patients.
Neutralizing
anti-receptor-binding
domain
(RBD)
immunoglobulin
G
(IgG)
antibodies
were
identified
as
primary
correlate
for
Analysis
virus-specific
B
T
cell
suggested
generation
neutralizing
anti-RBD
IgG
may
have
depended
on
cognate
T-B
interactions
took
place
germinal
center,
potentially
acting
a
limiting
checkpoint.
High-dose
mycophenolate
mofetil,
an
immunosuppressive
drug,
was
associated
fewer
antigen-specific
follicular
helper
(TFH)
cells
after
vaccination;
this
patients
recently
infected
SARS-CoV-2.
Last,
we
that,
independent
prospective
cohorts,
administration
third
dose
SARS-CoV-2
mRNA
vaccine
restored
titers
about
40%
individuals
had
previously
responded
doses
vaccine.
Together,
findings
suggest
improves
RBD-specific
treated
drugs.
Science,
Journal Year:
2021,
Volume and Issue:
374(6572)
Published: Oct. 15, 2021
Immune
memory
after
vaccination
Vaccination
against
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
has
proven
highly
effective
at
preventing
COVID-19.
However,
the
evolution
of
viral
variants,
and
waning
antibody
levels
over
time,
raise
questions
regarding
longevity
vaccine-induced
immune
protection.
Goel
et
al
.
examined
B
T
lymphocyte
responses
in
individuals
who
received
SARS-CoV-2
messenger
RNA
vaccines.
They
performed
a
6-month
longitudinal
study
never
had
infection
compared
with
people
recovered
from
SARS-CoV-2.
Humoral
cellular
was
observed
vaccinated
individuals,
as
were
functional
Alpha
(B.1.1.7),
Beta
(B.1.351),
Delta
(B.1.617.2)
variants.
Analysis
cell
activity
suggested
that
robust
may
prevent
hospitalization
by
limiting
development
disease.
—PNK
Cell,
Journal Year:
2022,
Volume and Issue:
185(6), P. 1025 - 1040.e14
Published: Jan. 25, 2022
During
the
SARS-CoV-2
pandemic,
novel
and
traditional
vaccine
strategies
have
been
deployed
globally.
We
investigated
whether
antibodies
stimulated
by
mRNA
vaccination
(BNT162b2),
including
third-dose
boosting,
differ
from
those
generated
infection
or
adenoviral
(ChAdOx1-S
Gam-COVID-Vac)
inactivated
viral
(BBIBP-CorV)
vaccines.
analyzed
human
lymph
nodes
after
for
correlates
of
serological
differences.
Antibody
breadth
against
variants
is
lower
compared
with
all
vaccines
evaluated
but
improves
over
several
months.
Viral
variant
elicits
variant-specific
antibodies,
prior
imprints
responses
toward
Wuhan-Hu-1
rather
than
antigens.
In
contrast
to
disrupted
germinal
centers
(GCs)
in
during
infection,
stimulates
robust
GCs
containing
spike
antigen
up
8
weeks
postvaccination
some
cases.
antibody
specificity,
breadth,
maturation
are
affected
imprinting
exposure
history
distinct
histological
antigenic
contexts
vaccination.
Immunological Reviews,
Journal Year:
2022,
Volume and Issue:
310(1), P. 6 - 26
Published: June 5, 2022
Antibodies
against
epitopes
in
S1
give
the
most
accurate
CoP
infection
by
SARS-CoV-2
coronavirus.
Measurement
of
those
antibodies
neutralization
or
binding
assays
both
have
predictive
value,
with
antibody
titers
giving
highest
statistical
correlation.
However,
protective
functions
are
multiple.
multiple
other
than
influence
efficacy.
The
role
cellular
responses
can
be
discerned
respect
to
CD4
Science,
Journal Year:
2022,
Volume and Issue:
378(6622), P. 899 - 904
Published: Nov. 24, 2022
Seasonal
influenza
vaccines
offer
little
protection
against
pandemic
virus
strains.
It
is
difficult
to
create
effective
prepandemic
because
it
uncertain
which
subtype
will
cause
the
next
pandemic.
In
this
work,
we
developed
a
nucleoside-modified
messenger
RNA
(mRNA)-lipid
nanoparticle
vaccine
encoding
hemagglutinin
antigens
from
all
20
known
A
subtypes
and
B
lineages.
This
multivalent
elicited
high
levels
of
cross-reactive
subtype-specific
antibodies
in
mice
ferrets
that
reacted
encoded
antigens.
Vaccination
protected
challenged
with
matched
mismatched
viral
strains,
was
at
least
partially
dependent
on
antibodies.
Our
studies
indicate
mRNA
can
provide
antigenically
variable
viruses
by
simultaneously
inducing
multiple
Immunological Reviews,
Journal Year:
2022,
Volume and Issue:
310(1), P. 27 - 46
Published: June 22, 2022
Immunological
memory
is
the
basis
of
protective
immunity
provided
by
vaccines
and
previous
infections.
can
develop
from
multiple
branches
adaptive
immune
system,
including
CD4
T
cells,
CD8
B
long-lasting
antibody
responses.
Extraordinary
progress
has
been
made
in
understanding
to
SARS-CoV-2
infection
COVID-19
vaccines,
addressing
development;
quantitative
qualitative
features
different
cellular
anatomical
compartments;
durability
each
component
antibodies.
Given
sophistication
measurements;
size
human
studies;
use
longitudinal
samples
cross-sectional
head-to-head
comparisons
between
or
for
1
year
already
supersedes
that
any
other
acute
infectious
disease.
This
knowledge
may
help
inform
public
policies
regarding
as
well
scientific
development
future
against
diseases.
Annual Review of Immunology,
Journal Year:
2023,
Volume and Issue:
41(1), P. 343 - 373
Published: Feb. 8, 2023
A
large
body
of
evidence
generated
in
the
last
two
and
a
half
years
addresses
roles
T
cells
SARS-CoV-2
infection
following
vaccination.
Infection
or
vaccination
induces
multi-epitope
CD4
CD8
cell
responses
with
polyfunctionality.
Early
have
been
associated
mild
COVID-19
outcomes.
In
concert
animal
model
data,
these
results
suggest
that
while
antibody
are
key
to
prevent
infection,
may
also
play
valuable
reducing
disease
severity
controlling
infection.
memory
after
is
sustained
for
at
least
six
months.
While
neutralizing
impacted
by
variants,
most
preserved.
This
review
highlights
extensive
progress
made,
data
knowledge
gaps
remain,
our
understanding
vaccines.