Frontiers in Immunology,
Journal Year:
2023,
Volume and Issue:
13
Published: Jan. 10, 2023
Patients
with
hematological
malignancies
are
prioritized
for
COVID-19
vaccine
due
to
their
high
risk
severe
SARS-CoV-2
infection-related
disease
and
mortality.
To
understand
T
cell
immunity,
its
long-term
persistence,
correlation
antibody
response,
we
evaluated
the
BNT162b2
mRNA
vaccine-specific
immune
response
in
chronic
lymphocytic
leukemia
(CLL)
myeloid
dysplastic
syndrome
(MDS)
patients.
Longitudinal
analysis
of
CD8
+
cells
using
DNA-barcoded
peptide-MHC
multimers
covering
full
Spike-protein
(415
peptides)
showed
activation
persistence
memory
up
six
months
post-vaccination.
Surprisingly,
a
higher
frequency
vaccine-induced
antigen-specific
was
observed
patient
group
compared
healthy
donor
group.
Furthermore,
importantly,
immunization
second
booster
dose
significantly
increased
as
well
total
number
specificities.
Altogether
59
vaccine-derived
immunogenic
responses
were
identified,
which
23
established
strong
immunodominance
NYNYLYRLF
(HLA-A24:02)
YLQPRTFLL
(HLA-A02:01)
epitopes.
In
summary,
mapped
booster-specific
enrichment
that
could
be
important
protection
this
Infectious Diseases and Therapy,
Journal Year:
2023,
Volume and Issue:
12(2), P. 367 - 387
Published: Jan. 9, 2023
Vaccines
developed
against
SARS-CoV-2
have
proven
to
be
highly
effective
in
preventing
symptomatic
infection.
Similarly,
prior
infection
with
has
been
shown
provide
substantial
protection
reinfection.
However,
it
become
apparent
that
the
provided
an
individual
after
either
vaccination
or
wanes
over
time.
Waning
is
driven
by
both
waning
immunity
time
since
initial
infection,
and
evolution
of
new
variants
SARS-CoV-2.
Both
antibody
T/B-cells
levels
investigated
as
potential
correlates
post-vaccination
post-infection.
The
activity
antibodies
some
insight
into
underlying
causes
protection.
This
review
seeks
summarise
what
currently
known
about
and/or
well
current
information
on
respective
T/B-cell
responses.
Nature Cancer,
Journal Year:
2021,
Volume and Issue:
2(12), P. 1321 - 1337
Published: Oct. 27, 2021
Patients
with
cancer
have
higher
COVID-19
morbidity
and
mortality.
Here
we
present
the
prospective
CAPTURE
study,
integrating
longitudinal
immune
profiling
clinical
annotation.
Of
357
patients
cancer,
118
were
SARS-CoV-2
positive,
94
symptomatic
2
died
of
COVID-19.
In
this
cohort,
83%
had
S1-reactive
antibodies
82%
neutralizing
against
wild
type
SARS-CoV-2,
whereas
antibody
titers
Alpha,
Beta
Delta
variants
substantially
reduced.
levels
decreased
in
13%
patients,
remained
stable
for
up
to
329
days.
also
detectable
SARS-CoV-2-specific
T
cells
CD4
Frontiers in Immunology,
Journal Year:
2022,
Volume and Issue:
13
Published: Aug. 29, 2022
To
evaluate
the
immunogenicity
of
COVID-19
vaccines
in
patients
with
diabetes
mellitus
(DM)
through
a
systematic
approach.A
comprehensive
search
was
conducted
PubMed,
Scopus,
and
Web
Science
no
time
restrictions.
The
based
on
three
main
concepts:
Covid-19,
Vaccine
Diabetes
Mellitus.After
excluding
irrelevant
studies,
16
studies
remained
for
quantitative
assay.
Among
sixteen
eleven
had
controls.
Type
specifically
mentioned
six
(T2DM;
n=4,
T1DM
T2DM;
n=2).
Twelve
included
were
that
mRNA
(i.e.
BNT162b2
mRNA-1273)
DM,
five
vector-based
Ad5-nCoV
ChAdOx1-S),
assessed
including
inactivated
BBV-152,
CoronaVac,
Sinopharm
or
SinoVac).
Most
current
indicate
lower
antibody
response
DM
compared
to
individuals
without
after
second
dose
vaccine
irrespective
type.
Several
have
shown
higher
age
BMI
are
associated
response,
while
optimum
glycemic
control
GFR
among
DM.Immunogenicity
has
mostly
been
reported
be
healthy
There
also
few
assessing
variables
significantly
affect
this
association,
age,
type
diabetes,
BMI,
eGFR.
Investigating
these
associations
could
help
us
provide
most
advantageous
condition
before,
during
vaccination
response.
Many
unresolved
issues
concerning
potential
factors
affecting
immunogenicity,
vaccine,
numbers
administered
doses,
re-vaccination
intervals
hyperglycemia
need
addressed
future
research.
Pathogens and Global Health,
Journal Year:
2022,
Volume and Issue:
116(5), P. 269 - 281
Published: Jan. 31, 2022
This
study
aims
to
estimate
the
prevalence
and
longevity
of
detectable
SARS-CoV-2
antibodies
T
B
memory
cells
after
recovery.
In
addition,
COVID-19
reinfection
preventive
efficacy
previous
infection
with
were
investigated.
A
synthesis
existing
research
was
conducted.
The
Cochrane
Library,
China
Academic
Journals
Full
Text
Database,
PubMed,
Scopus,
preprint
servers
searched
for
studies
conducted
between
1
January
2020
April
2021.
Included
assessed
methodological
quality
pooled
estimates
relevant
outcomes
obtained
in
a
meta-analysis
using
bias
adjusted
method.
Proportions
synthesized
Freeman-Tukey
double
arcsine
transformation
binary
odds
ratio
(OR).
Heterogeneity
I2
Cochran's
Q
statistics
publication
Doi
plots.
Fifty-four
from
18
countries,
around
12,000,000
individuals,
followed
up
8
months
recovery,
included.
At
6–8
specific
immunological
remained
high;
IgG
–
90.4%
(95%CI
72.2–99.9,
=
89.0%),
CD4+
91.7%
78.2–97.1y),
80.6%
65.0–90.2)
0.2%
0.0–0.7,
98.8).
Individuals
previously
infected
had
an
81%
reduction
(OR
0.19,
95%
CI
0.1–0.3,
90.5%).
Around
90%
recovered
individuals
evidence
SARS-CoV-2,
at
recovery
low
risk
reinfection.RegistrationPROSPERO:
CRD42020201234
Viruses,
Journal Year:
2022,
Volume and Issue:
14(7), P. 1493 - 1493
Published: July 8, 2022
Emerging
and
re-emerging
viral
diseases
have
increased
in
number
geographical
extent
during
the
last
decades.
Examples
include
current
COVID-19
pandemic
recent
epidemics
of
Chikungunya,
Ebola,
Zika
viruses.
Immune
responses
to
viruses
been
well-characterised
within
innate
adaptive
immunity
pathways
with
outcome
following
infection
predominantly
attributed
properties
virus
circumstances
infection.
Perhaps
belief
that
immune
system
is
often
considered
as
a
reactive
component
host
defence,
springing
into
action
when
threat
detected,
has
contributed
poorer
understanding
inherent
differences
an
individual’s
absence
any
pathology.
In
this
review,
we
focus
on
how
these
factors
(age,
ethnicity,
underlying
pathologies)
may
skew
T
helper
cell
response,
thereby
influencing
but
also
whether
can
use
biases
predict
patients
at
risk
deviant
response
apply
strategies
avoid
or
overcome
them.