SARS-CoV-2 XBB.1.5 mRNA booster vaccination elicits limited mucosal immunity
Science Translational Medicine,
Journal Year:
2024,
Volume and Issue:
16(770)
Published: Oct. 23, 2024
Current
COVID-19
vaccines
provide
robust
protection
against
severe
disease
but
minimal
acquisition
of
infection.
Intramuscularly
administered
induce
serum
neutralizing
antibodies
(NAbs),
their
ability
to
boost
mucosal
immune
responses
remains
be
determined.
In
this
study,
we
show
that
the
XBB.1.5
messenger
RNA
(mRNA)
boosters
result
in
increased
neutralization
multiple
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
variants
humans,
including
dominant
circulating
variant
JN.1.
contrast,
found
mRNA
booster
did
not
augment
NAbs
or
IgA
responses,
although
SARS-CoV-2
XBB
infection
substantially
antibody
responses.
These
data
demonstrate
current
enhance
peripheral
do
robustly
increase
Our
highlight
a
separation
between
and
systems
humans
emphasize
importance
developing
next-generation
immunity
protect
virus
infections.
Language: Английский
A SARS-CoV-2 mucosal nanovaccine based on assembly of maltodextrin, STING agonist and polyethyleneimine
International Journal of Biological Macromolecules,
Journal Year:
2025,
Volume and Issue:
unknown, P. 139395 - 139395
Published: Jan. 1, 2025
Language: Английский
Evaluation of a novel intramuscular prime/intranasal boost vaccination strategy against influenza in the pig model
PLoS Pathogens,
Journal Year:
2024,
Volume and Issue:
20(8), P. e1012393 - e1012393
Published: Aug. 8, 2024
Live-attenuated
influenza
vaccines
(LAIV)
offer
advantages
over
the
commonly
used
inactivated
split
vaccines.
However,
finding
optimal
balance
between
sufficient
attenuation
and
immunogenicity
has
remained
a
challenge.
We
recently
developed
an
alternative
LAIV
based
on
2009
pandemic
H1N1
virus
with
truncated
NS1
protein
lacking
PA-X
expression
(NS1(1-126)-ΔPAX).
This
showed
blunted
replication
elicited
strong
innate
immune
response.
In
present
study,
we
evaluated
efficacy
of
this
vaccine
candidate
in
porcine
animal
model
as
pertinent
vivo
system.
Immunization
pigs
via
nasal
route
novel
NS1(1-126)-ΔPAX
did
not
cause
disease
mucosal
response
that
completely
blocked
homologous
challenge
respiratory
tract.
observed
prolonged
shedding
our
from
upper
To
improve
safety,
prime/boost
vaccination
strategy
combining
primary
intramuscular
immunization
haemagglutinin-encoding
propagation-defective
vesicular
stomatitis
(VSV)
replicon,
followed
by
secondary
route.
two-step
procedure
significantly
reduced
shedding,
increased
production
specific
serum
IgG,
neutralizing
antibodies,
Th1
memory
cells,
resulted
sterilizing
immunity
against
conclusion,
prime/intranasal
boost
regimen
interferes
transmission,
feature
will
help
combat
epidemics
pandemics.
Language: Английский