Intranasal Inoculation of Cationic Crosslinked Carbon Dots‐Adjuvanted Respiratory Syncytial Virus F Subunit Vaccine Elicits Mucosal and Systemic Humoral and Cellular Immunity
Lei Hong,
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Aqu Alu,
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H. J. Yang
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et al.
MedComm,
Journal Year:
2025,
Volume and Issue:
6(4)
Published: March 24, 2025
ABSTRACT
Respiratory
syncytial
virus
(RSV)
causes
severe
acute
lower
respiratory
tract
infections,
especially
in
infants
and
the
elderly.
Developing
an
RSV
vaccine
that
promotes
a
robust
mucosal
immune
response
is
necessary
to
successfully
prevent
viral
transmission
development
of
disease.
We
previously
reported
crosslinked
carbon
dots
(CCD)
may
be
excellent
adjuvant
candidate
for
intranasal
(IN)
protein
subunit
vaccines.
Considering
strong
immunogenicity
prefused
F
(preF),
we
prepared
IN
composed
CCD
preF
as
antigen
(CCD/preF)
evaluated
induced
antigen‐specific
humoral
cellular
immunity.
found
immunization
with
CCD/preF
elicited
serum
IgG
responses
immunity,
including
secreted
IgA
antibodies,
tissue‐resident
memory
T
(T
RM
)
cells,
B
which
lasted
at
least
1
year.
In
addition,
combination
intramuscular
stronger
systemic
Together,
this
study
proved
high
vaccines
supported
university
adjuvant,
supporting
further
larger
animal
models
clinical
studies.
Language: Английский
AH-6809 mediated regulation of lung adenocarcinoma metastasis through NLRP7 and prognostic analysis of key metastasis-related genes
Feng Xu,
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Wei Wu,
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Feifei Liu
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et al.
Frontiers in Pharmacology,
Journal Year:
2024,
Volume and Issue:
15
Published: Dec. 4, 2024
Lung
adenocarcinoma
(LUAD)
has
become
one
of
the
leading
causes
cancer-related
deaths
globally,
with
metastasis
representing
most
lethal
stage
disease.
Despite
significant
advances
in
diagnostic
and
therapeutic
strategies
for
LUAD,
mechanisms
enabling
cancer
cells
to
breach
blood-brain
barrier
remain
poorly
understood.
While
genomic
profiling
shed
light
on
nature
primary
tumors,
genetic
drivers
clinical
relevance
LUAD
are
still
largely
unexplored.
Language: Английский
Paromomycin targets HDAC1-mediated SUMOylation and IGF1R translocation in glioblastoma
Min Zhong,
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Yuejie Guo,
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Ning Luo
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et al.
Frontiers in Pharmacology,
Journal Year:
2024,
Volume and Issue:
15
Published: Dec. 11, 2024
Objective
This
study
investigates
the
effects
of
Paromomycin
on
SUMOylation-related
pathways
in
glioblastoma
(GBM),
specifically
targeting
HDAC1
inhibition.
Methods
Using
TCGA
and
GTEx
datasets,
we
identified
genes
associated
with
GBM
prognosis.
Molecular
docking
analysis
suggested
as
a
potential
inhibitor.
In
vitro
assays
U-251MG
cells
were
performed
to
assess
Paromomycin’s
cell
viability,
SUMOylation
gene
expression,
IGF1R
translocation
using
CCK8
assays,
qRT-PCR,
immunofluorescence.
Results
treatment
led
dose-dependent
reduction
colony
formation,
migration.
It
modulated
SUMO1
expression
decreased
nuclear
translocation,
an
effect
reversible
by
inhibitor
Trochostatin
A
(TSA),
suggesting
involvement
SUMO1-regulated
pathways.
Conclusion
highlights
therapeutic
agent
for
HDAC1-mediated
influencing
warranting
further
investigation
its
clinical
application.
Language: Английский