Microneedle patch-involved local therapy synergized with immune checkpoint inhibitor for pre- and post-operative cancer treatment
Yue Yin,
No information about this author
Lu Tang,
No information about this author
Yuqi Cao
No information about this author
et al.
Journal of Controlled Release,
Journal Year:
2025,
Volume and Issue:
379, P. 678 - 695
Published: Jan. 24, 2025
Language: Английский
A Nano-Strategy for Advanced Triple-Negative Breast Cancer Therapy by Regulating Intratumoral Microbiota
Jifan Gao,
No information about this author
Lu Tang,
No information about this author
Cong Fu
No information about this author
et al.
Nano Letters,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 3, 2025
Intratumoral
microbiota
have
been
identified
as
a
component
of
the
tumor
microenvironment
that
regulates
metastatic
behavior
tumors.
They
serve
not
only
indicators
pathology
but
also
potential
drug
targets
in
cancer
therapy.
Herein,
multifunctional
nanoplatform
(DD@FEL)
is
prepared
by
combining
antibiotic
doxycycline
(DOXY)
can
combat
intratumoral
and
chemotherapeutic
doxorubicin
(DOX)
ergosterol-originated
liposome.
Specially,
ergosterol
utilized
substitute
for
cholesterol
liposomes
to
exert
pharmacological
activity.
Mechanistically,
DD@FEL
leveraged
DOXY
inhibit
metastasis
based
on
regulation
microbiota,
which
synergizes
with
effect
DOX,
eventually
inhibiting
progression
triple-negative
breast
(TNBC).
Verified
both
vitro
vivo,
effectively
exerts
cytotoxic
TNBC
cells,
delays
growth
primary
TNBC,
attenuates
development
its
lung
metastasis,
providing
promising
therapeutic
strategy
control
orthotopic
TNBC.
Language: Английский
Treating and Protecting against Recurrent Vulvovaginal Candidiasis Using the Vaginal Epithelial Cell Membrane-Based Photoimmunotherapeutic Nanoplatform
Ledan Wang,
No information about this author
Yijing Lin,
No information about this author
Shuangshuang Liu
No information about this author
et al.
ACS Nano,
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 15, 2025
Recurrent
vulvovaginal
candidiasis
(RVVC)
is
an
opportunistic
infection
predominantly
caused
by
Candida
albicans
(C.
albicans)
and
particularly
prevalent
among
individuals
on
immunosuppressants.
Currently,
there
are
no
FDA-approved
therapies
for
specifically
controlling
RVVC,
mainly
due
to
the
need
therapeutics
against
RVVC
that
require
both
antifungal
treatments
resolve
active
infections
strategies
prevent
recurrence.
This
study
introduces
a
biomimetic
photoimmunotherapeutic
nanoplatform
consisting
of
adjuvant-encapsulated
polymeric
core
stabilized
photosensitizer-loaded
vaginal
epithelial
cell
membrane
coating
treat
protect
RVVC.
With
its
camouflaging,
nanoplatforms
target
enhance
adherence
intravaginal
site
C.
infection,
allowing
resist
being
flushed
away
fluids.
Upon
subsequent
near-infrared
irradiation,
nanoplatform's
targeted
photothermal
power
effectively
eliminates
while
minimizing
thermal
damage
surrounding
healthy
tissue.
Postphotothermal
treatment,
generated
albicans-based
debris
candidalysin-captured
(serving
as
nanotoxoid),
along
with
adjuvant,
processed
resident
antigen-presenting
cells
promote
multiantigenic
immunity.
response
provides
protection
secondary
(RVVC
model)
albicans-induced
systemic
even
under
immunosuppressive
conditions
(septicemia
model).
Notably,
anti-C.
antibodies
produced
in
pretreated
mice
exhibit
comparable
affinity
clinically
isolated
strains,
indicating
potential
clinical
application.
Overall,
this
underscores
proposed
effective
treatment
prevention
Language: Английский
Bioorthogonal Engineering of Bacterial Outer Membrane Vesicles for NIR-II Fluorescence Imaging-Guided Synergistic Enhanced Immunotherapy
Na Li,
No information about this author
Minghui Wang,
No information about this author
Fen Liu
No information about this author
et al.
Analytical Chemistry,
Journal Year:
2024,
Volume and Issue:
96(49), P. 19585 - 19596
Published: Nov. 27, 2024
The
efficacy
of
immunotherapy
in
treating
triple-negative
breast
cancer
(TNBC)
has
been
restricted
due
to
its
low
immunogenicity
and
suppressive
immune
microenvironment.
Bacterial
outer
membrane
vesicles
(OMVs)
have
emerged
as
innovative
immunotherapeutic
agents
antitumor
therapy
by
stimulating
the
innate
system,
but
intricate
modifications
undesirable
multiple
dose
administration
severely
hinder
their
utility.
Herein,
a
two-step
bacterial
metabolic
labeling
technique
was
utilized
for
bioorthogonal
engineering
OMVs.
At
first,
d-propargylglycine
(DPG,
an
alkyne-containing
d-amino
acid)
introduced
into
incubation
process
probiotic
Escherichia
coli
1917
(Ecn)
produce
DPG-functionalized
OMVs,
which
were
subsequently
conjugated
with
azide-functionalized
new
indocyanine
green
(IR820)
yield
OMV-DPG-IR820.
combination
phototherapy
immunostimulation
OMV-DPG-IR820
effectively
arouses
adaptive
responses,
causing
maturation
dendritic
cells,
infiltration
T
repolarization
M2
macrophage
M1
macrophage,
upregulation
inflammatory
factors.
Remarkably,
demonstrated
tumor-targeting
capabilities
guidance
provided
near-infrared
II
(NIR-II)
fluorescence
imaging,
leading
remarkable
inhibition
on
both
primary
distant
tumors
preventing
metastasis
without
noticeable
adverse
reactions.
This
study
elucidates
sophisticated
strategy
design
production
functionalized
OMVs
provides
novel
perspectives
microbiome-mediated
reversal
TNBC
through
precise
efficient
immunotherapy.
Language: Английский