Scientific Reports,
Год журнала:
2023,
Номер
13(1)
Опубликована: Май 20, 2023
Abstract
Severe
fever
with
thrombocytopenia
syndrome
virus
was
first
discovered
in
2009
as
the
causative
agent
of
severe
syndrome.
Despite
its
potential
threat
to
public
health,
no
prophylactic
vaccine
is
yet
available.
This
study
developed
a
heterologous
prime-boost
strategy
comprising
priming
recombinant
replication-deficient
human
adenovirus
type
5
(rAd5)
expressing
surface
glycoprotein,
Gn,
and
boosting
Gn
protein.
vaccination
regimen
induced
balanced
Th1/Th2
immune
responses
resulted
potent
humoral
T
cell-mediated
mice.
It
elicited
high
neutralizing
antibody
titers
both
mice
non-human
primates.
Transcriptome
analysis
revealed
that
rAd5
proteins
adaptive
innate
pathways,
respectively.
provides
immunological
mechanistic
insight
into
this
paves
way
for
future
strategies
against
emerging
infectious
diseases.
Annual Review of Immunology,
Год журнала:
2023,
Номер
41(1), С. 343 - 373
Опубликована: Фев. 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.
Frontiers in Immunology,
Год журнала:
2022,
Номер
13
Опубликована: Авг. 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.
Transplant Infectious Disease,
Год журнала:
2023,
Номер
25(S1)
Опубликована: Июль 29, 2023
Abstract
Revaccination
after
receipt
of
a
hematopoietic
cell
transplant
(HCT)
or
cellular
therapies
is
pillar
patient
supportive
care,
with
the
potential
to
reduce
morbidity
and
mortality
linked
vaccine‐preventable
infections.
This
review
synthesizes
national,
international,
expert
consensus
vaccination
schedules
post‐HCT
presents
evidence
regarding
efficacy
newer
vaccine
formulations
for
pneumococcus,
recombinant
zoster
vaccine,
coronavirus
disease
2019
in
patients
hematological
malignancy.
post‐cellular
are
less
well
defined.
highlights
important
considerations
around
poor
response,
seroprevalence
preservation
therapies,
optimal
timing
revaccination.
Future
research
should
assess
immunogenicity
real‐world
effectiveness
new
and/or
therapy,
including
analysis
response
that
relates
target
therapies.
Journal for ImmunoTherapy of Cancer,
Год журнала:
2023,
Номер
11(2), С. e006246 - e006246
Опубликована: Фев. 1, 2023
Background
Immune
checkpoint
inhibitors
(ICI)
can
cause
off-target
inflammatory
and
immune-related
adverse
events
(irAE).
Conceivably,
COVID-19
vaccination
could
trigger
an
immune
response
that
induce
or
aggravate
irAE.
Methods
The
objective
of
this
systematic
review
is
to
appraise
the
efficacy
safety
in
patients
with
cancer
treated
ICI.
literature
search
was
performed
PubMed
Embase
English
from
December
2019
February
2022.
included
clinical
trials,
observational
cohort
studies,
case
series,
reports
reporting
on
vaccines
Outcomes
interest
seroconversion,
SARS-CoV-2
infection
rate,
severe
COVID-19,
mortality
rate.
Incidence
ICI
irAEs
also
ascertained
as
well
vaccine
events.
A
meta-analysis
conducted
estimate
pooled
effect
sizes
outcomes
when
possible,
using
random
effects
models.
Results
Overall,
19
studies
were
for
analysis
(n=10
865
2477
receiving
ICI).
We
analyzed
15
1
cross-sectional
study,
3
reports.
There
no
statistically
significant
differences
seroconversion
rates
after
second
dose
comparing
without
(risk
ratio,
RR
0.97,
95%
CI
0.92
1.03)
active
treatment
(RR
1.00,
0.96
1.04).
a
higher
probability
compared
chemotherapy
1.09,
1.00
1.18).
In
single
study
ICI,
observed
risk
irAE
between
those
inactivated
unvaccinated
(pneumonitis
0.88,
0.33
2.3;
rash
1.03,
0.66
1.62;
arthralgia
0.94,
0.51
1.75).
other
types
vaccinated
vs
not
most
common
vaccine-related
local
pain
fatigue.
quality
evidence
rated
very
low.
Conclusion
appears
be
effective
safe
Although
severe
coronavirus
disease
2019
(COVID-19)
and
hospitalization
associated
with
COVID-19
are
generally
preventable
among
healthy
vaccine
recipients,
patients
immunosuppression
have
poor
immunogenic
responses
to
vaccines
remain
at
high
risk
of
infection
SARS-CoV-2
hospitalization.
In
addition,
monoclonal
antibody
therapy
is
limited
by
the
emergence
novel
variants
that
serially
escaped
neutralization.
this
context,
there
interest
in
understanding
clinical
benefit
convalescent
plasma
collected
from
persons
who
been
both
naturally
infected
vaccinated
against
("vax-plasma").
Thus,
we
report
outcome
386
immunocompromised
outpatients
were
diagnosed
received
contemporary
COVID-19-specific
therapeutics
(standard-of-care
group)
a
subgroup
also
concomitant
treatment
very
titer
(vax-plasma
specific
focus
on
rates.
The
overall
rate
was
2.2%
(5
225
patients)
vax-plasma
group
6.2%
(10
161
standard-of-care
group,
which
corresponded
relative
reduction
65%
(
Abstract
Individuals
with
hematologic
malignancies
are
at
increased
risk
for
severe
coronavirus
disease
2019
(COVID-19),
yet
profound
analyses
of
COVID-19
vaccine-induced
immunity
scarce.
Here
we
present
an
observational
study
expanded
methodological
analysis
a
longitudinal,
primarily
BNT162b2
mRNA-vaccinated
cohort
60
infection-naive
individuals
B
cell
lymphomas
and
multiple
myeloma.
We
show
that
many
these
individuals,
despite
markedly
lower
anti-spike
IgG
titers,
rapidly
develop
potent
infection
neutralization
capacities
against
several
acute
respiratory
syndrome
2
variants
concern
(VoCs).
The
observed
capacity
per
antibody
unit
was
paralleled
by
early
step
increase
in
avidity
between
the
second
third
vaccination.
All
malignancies,
including
those
depleted
cells
myeloma,
exhibited
robust
T
response
to
peptides
derived
from
spike
protein
VoCs
Delta
Omicron
(BA.1).
Consistently,
breakthrough
infections
were
mainly
mild
moderate
severity.
conclude
vaccination
can
induce
broad
antiviral
ultrapotent
neutralizing
antibodies
high
different
malignancies.