PLoS ONE,
Journal Year:
2025,
Volume and Issue:
20(4), P. e0320744 - e0320744
Published: April 28, 2025
During
the
COVID-19
pandemic,
hematopoietic
stem
cell
transplant
(HSCT)
recipients
had
elevated
mortality
rates
from
SARS-CoV-2
infection,
ranging
between
10–40%.
mRNA
vaccines
are
important
tools
in
preventing
severe
disease,
yet
their
efficacy
post-transplant
remains
unclear,
especially
patients
subjected
to
myeloablative
chemotherapy
and
immunosuppression.
We
evaluated
humoral
adaptive
immune
responses
vaccination
series
42
HSCT
5
healthy
controls.
Post-vaccination
were
assessed
by
anti-spike
IgG
nucleocapsid
levels,
antigen
specific
T
activity.
Immune
profiling
was
performed
using
clinical
flow
mass
cytometry.
Patients
selected
based
on
cellular
for
single-cell
RNA
with
TCR
BCR
sequencing.
Our
studies
revealed
defects
memory
cells
that
correlated
an
absence
of
response
despite
nearly
universal
response.
Several
a
robust
antibody
developed
but
none
disease
or
died
infection.
Journal of Medical Virology,
Journal Year:
2023,
Volume and Issue:
95(2)
Published: Feb. 1, 2023
Abstract
Messenger
RNA
(mRNA)
vaccines
against
COVID‐19
are
the
first
authorized
biological
preparations
developed
using
this
platform.
During
pandemic,
their
administration
has
been
proven
to
be
a
life‐saving
intervention.
Here,
we
review
main
advantages
of
mRNA
vaccines,
identify
further
technological
challenges
met
during
development
platform,
and
provide
an
update
on
clinical
progress
leading
vaccine
candidates
different
viruses
that
include
influenza
viruses,
human
immunodeficiency
virus
1,
respiratory
syncytial
virus,
Nipah
Zika
cytomegalovirus,
Epstein‐Barr
virus.
The
prospects
manufacturing
in
low‐income
countries
also
discussed.
ongoing
interest
research
technology
likely
overcome
some
existing
for
(e.g.,
related
storage
conditions
immunogenicity
components
lipid
nanoparticles)
enhance
portfolio
diseases
which
classical
formulations
already
authorized.
It
may
open
novel
pathways
protection
infections
consequences
no
safe
efficient
immunization
methods
currently
available.
Vaccines,
Journal Year:
2024,
Volume and Issue:
12(1), P. 71 - 71
Published: Jan. 11, 2024
The
concept
of
DNA
vaccination
was
introduced
in
the
early
1990s.
Since
then,
advancements
augmentation
immunogenicity
vaccines
have
brought
this
technology
to
market,
especially
veterinary
medicine,
prevent
many
diseases.
Along
with
successful
COVID
mRNA
vaccines,
first
vaccine
for
human
use,
Indian
ZyCovD
against
SARS-CoV-2,
approved
2021.
In
current
review,
we
give
an
overview
focusing
on
science,
including
adjuvants
and
delivery
methods.
We
then
cover
some
emerging
science
field
notably
efforts
optimize
systems,
better
engineer
apparatuses,
identify
optimal
sites,
personalize
cancer
immunotherapy
through
vaccination,
enhance
adjuvant
gene
adjuvants,
off-target
heritable
immunity
epigenetic
modification,
predict
epitopes
bioinformatic
approaches.
also
discuss
major
limitations
aim
address
theoretical
concerns.
BMJ Medicine,
Journal Year:
2023,
Volume and Issue:
2(1), P. e000468 - e000468
Published: Nov. 1, 2023
The
T
cell
memory
response
is
a
crucial
component
of
adaptive
immunity
responsible
for
limiting
or
preventing
viral
reinfection.
after
infection
with
the
SARS-CoV-2
virus
vaccination
broad,
and
spans
multiple
proteins
epitopes,
about
20
in
each
individual.
So
far
long
lasting
provides
high
level
cross
reactivity
hence
resistance
to
escape
by
variants
virus,
such
as
omicron
variant.
All
current
vaccine
regimens
tested
produce
robust
responses,
heterologous
will
probably
enhance
protective
responses
through
increased
breadth.
could
have
major
role
protecting
against
severe
covid-19
disease
rapid
clearance
early
presentation
presence
reactive
cells
might
this
protection.
likely
provide
ongoing
protection
admission
hospital
death,
development
pan-coronovirus
future
proof
new
pandemic
strains.
Science Advances,
Journal Year:
2024,
Volume and Issue:
10(8)
Published: Feb. 23, 2024
Messenger
RNA
(mRNA)
vaccines
were
highly
effective
against
the
ancestral
SARS-CoV-2
strain,
but
efficacy
of
bivalent
mRNA
boosters
XBB
variants
was
substantially
lower.
Here,
we
show
limited
durability
neutralizing
antibody
(NAb)
responses
and
isotype
switching
to
immunoglobulin
G4
(IgG4)
following
boosting.
Bivalent
boosting
elicited
modest
XBB.1-,
XBB.1.5-,
XBB.1.16-specific
NAbs
that
waned
rapidly
within
3
months.
In
contrast,
induced
more
robust
sustained
WA1/2020
suggesting
immune
imprinting.
Following
boosting,
serum
primarily
IgG2
IgG4
with
poor
Fc
functional
activity.
a
third
monovalent
immunization
boosted
all
isotypes
including
IgG1
IgG3
These
data
substantial
imprinting
for
spike
important
implications
future
booster
designs
strategies.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 10, 2025
SUMMARY
The
long-term
effects
of
repeated
COVID-19
vaccinations
on
adaptive
immunity
remain
incompletely
understood.
Here,
we
conducted
a
comprehensive
three-year
longitudinal
study
examining
T
cell
and
antibody
responses
in
78
vaccinated
individuals
without
reported
symptomatic
infections.
We
observed
distinct
dynamics
Spike-specific
humoral
cellular
immune
across
multiple
vaccine
doses.
While
titers
incrementally
increased
stabilized
with
each
booster,
rapidly
plateaued,
maintaining
remarkable
stability
CD4+
CD8+
subsets.
Notably,
approximately
30%
participants
showed
reactivity
to
non-Spike
antigens,
consistent
asymptomatic
Single-cell
RNA
sequencing
revealed
diverse
landscape
phenotypes,
no
evidence
exhaustion
or
significant
functional
impairment.
However,
qualitative
changes
were
infection,
exhibiting
unique
immunological
characteristics,
including
frequencies
Th17-like
cells
GZMKhi/IFNR
Remarkably,
this
group
associated
progressive
increase
regulatory
cells,
potentially
indicating
balanced
response
that
may
mitigate
immunopathology.
By
regularly
stimulating
memory,
boosters
contribute
stable
enhanced
response,
which
provide
better
protection
against
Journal of Virology,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 3, 2025
ABSTRACT
The
COVID-19
pandemic
has
greatly
enhanced
our
understanding
of
CD8+
T
cell
immunity
and
their
role
in
natural
infection
vaccine-induced
protection.
Rapid
early
SARS-CoV-2-specific
responses
have
been
associated
with
efficient
viral
clearance
mild
disease.
Virus-specific
can
compensate
for
waning,
morbidity-related,
iatrogenic
reduction
humoral
immunity.
After
or
vaccination,
memory
cells
are
formed,
which
mount
an
recall
response
the
event
breakthrough
help
to
protect
from
severe
Due
breadth
ability
target
mainly
highly
conserved
epitopes,
also
able
cross-recognize
epitopes
variants,
thus
maintaining
even
after
emergence
evolution.
In
some
cases,
however,
may
contribute
pathogenesis
COVID-19.
particular,
delayed
uncontrolled,
e.g.,
nonspecific
hyperactivated,
cytotoxic
linked
poor
outcomes.
this
minireview,
we
summarize
tremendous
knowledge
about
SARS-CoV-2
vaccination
that
gained
over
past
5
years,
while
highlighting
critical
gaps
remain.