Abstract
Rheumatoid
arthritis
(RA)
is
an
autoimmune
disorder
characterized
by
chronic
inflammation
of
the
synovial
joints
and
dysfunction
regulatory
T
cells
(Tregs)
in
peripheral
blood.
Therefore,
optimal
treatment
strategy
should
aim
to
eliminate
inflammatory
response
simultaneously
restore
immune
tolerance
Tregs
Accordingly,
we
developed
efferocytosis‐mimicking
nanovesicle
that
contains
three
functional
factors
for
immunomodulating
efferocytosis,
including
“find
me”
“eat
signals
professional
(macrophage)
or
non‐professional
phagocytes
(T
lymphocyte),
“apoptotic
metabolite”
metabolite
digestion.
We
showed
nanovesicles
targeted
inflamed
spleen
mice
with
collagen‐induced
arthritis,
further
recruiting
selectively
binding
macrophages
lymphocytes
induce
M2
macrophage
polarization
Treg
differentiation
helper
cell
17
(Th17)
recession.
Under
systemic
administration,
effectively
maintained
pro‐inflammatory
M1/anti‐inflammatory
balance
Treg/Th17
imbalance
blood
prevent
RA
progression.
This
study
demonstrates
potential
immunotherapy.
Abstract
Immunotherapies
have
revolutionized
the
treatment
paradigms
of
various
types
cancers.
However,
most
these
immunomodulatory
strategies
focus
on
harnessing
adaptive
immunity,
mainly
by
inhibiting
immunosuppressive
signaling
with
immune
checkpoint
blockade,
or
enhancing
immunostimulatory
bispecific
T
cell
engager
and
chimeric
antigen
receptor
(CAR)-T
cell.
Although
agents
already
achieved
great
success,
only
a
tiny
percentage
patients
could
benefit
from
immunotherapies.
Actually,
immunotherapy
efficacy
is
determined
multiple
components
in
tumor
microenvironment
beyond
immunity.
Cells
innate
arm
system,
such
as
macrophages,
dendritic
cells,
myeloid-derived
suppressor
neutrophils,
natural
killer
unconventional
also
participate
cancer
evasion
surveillance.
Considering
that
cornerstone
antitumor
response,
utilizing
immunity
provides
potential
therapeutic
options
for
control.
Up
to
now,
exploiting
agonists
stimulator
interferon
genes,
CAR-macrophage
-natural
therapies,
metabolic
regulators,
novel
exhibited
potent
activities
preclinical
clinical
studies.
Here,
we
summarize
latest
insights
into
roles
cells
discuss
advances
arm-targeted
strategies.
Biomolecules,
Год журнала:
2022,
Номер
12(5), С. 636 - 636
Опубликована: Апрель 25, 2022
Poly(α-L-glutamic
acid)
(PGA)
is
a
class
of
synthetic
polypeptides
composed
the
monomeric
unit
α-L-glutamic
acid.
Owing
to
their
biocompatibility,
biodegradability,
and
non-immunogenicity,
PGA-based
nanomaterials
have
been
elaborately
designed
for
drug
delivery
systems.
Relevant
studies
including
latest
research
results
on
discussed
in
this
work.
The
following
related
topics
are
summarized
as:
(1)
brief
description
strategies
PGAs;
(2)
an
elaborated
presentation
evolving
applications
PGA
areas
delivery,
rational
design,
precise
fabrication,
biological
evaluation;
(3)
profound
discussion
further
development
delivery.
In
summary,
unique
structures
superior
properties
enables
represent
as
enormous
potential
biomaterials-related
areas.
Abstract
Cell
membrane‐coated
nanoparticles
(CMNPs)
have
recently
emerged
as
a
promising
platform
for
cancer
therapy.
By
encapsulating
therapeutic
agents
within
cell
membrane‐derived
coating,
these
combine
the
advantages
of
synthetic
and
natural
membranes.
This
review
provides
comprehensive
overview
recent
advancements
in
utilizing
CMNPs
effective
drug
delivery
vehicles
The
synthesis
fabrication
methods
are
comprehensively
discussed.
Various
techniques,
such
extrusion,
sonication,
self‐assembly,
employed
to
coat
with
membranes
derived
from
different
types.
membrane
coating
enables
biocompatibility,
reducing
risk
an
immune
response
enhancing
stability
bloodstream.
Moreover,
functionalization
strategies
CMNPs,
primarily
chemical
modification,
genetic
engineering,
external
stimuli,
highlighted.
presence
specific
surface
markers
on
coated
allows
targeted
cells
maximizes
efficacy.
Preclinical
studies
therapy
demonstrated
successful
various
agents,
chemotherapeutic
drugs,
nucleic
acids,
immunotherapeutic
using
CMNPs.
Furthermore,
article
explores
future
directions
challenges
this
technology
while
offering
insights
into
its
clinical
potential.
The
innate
immune
system
serves
as
the
body's
first
line
of
defense,
utilizing
pattern
recognition
receptors
like
Toll-like
to
detect
pathogens
and
initiate
rapid
response
mechanisms.
Following
this
initial
response,
adaptive
immunity
provides
highly
specific
sustained
killing
via
B
cells,
T
antibodies.
Traditionally,
it
has
been
assumed
that
activates
immunity;
however,
recent
studies
have
revealed
more
complex
interactions.
This
review
a
detailed
dissection
composition
function
systems,
emphasizing
their
synergistic
roles
in
physiological
pathological
contexts,
providing
new
insights
into
link
between
these
two
forms
immunity.
Precise
regulation
both
systems
at
same
time
is
beneficial
fight
against
immune-related
diseases,
for
example,
cGAS-STING
pathway
found
play
an
important
role
infections
cancers.
In
addition,
paper
summarizes
challenges
future
directions
field
immunity,
including
latest
single-cell
sequencing
technologies,
CAR-T
cell
therapy,
checkpoint
inhibitors.
By
summarizing
developments,
aims
enhance
our
understanding
complexity
interactions
perspectives
system.
Asian Journal of Pharmaceutical Sciences,
Год журнала:
2025,
Номер
20(2), С. 101040 - 101040
Опубликована: Фев. 27, 2025
Cellular
hitchhiking
is
an
emerging
therapeutic
strategy
that
uses
endogenous
cell
migration
mechanism
to
deliver
therapeutics
specific
sites
in
the
body.
Owing
low
permeability
and
presence
of
blood-brain
barrier
(BBB),
targeted
delivery
limited,
leading
inadequate
localization
brain.
NCs
fail
extravasate
significantly
into
tumor
microenvironment
(TME),
demonstrating
poor
accumulation
penetration.
The
novel
cellular
concept
has
been
utilized
promote
systemic
half-life
targeting.
Neoplastic
neuroinflammatory
diseases
brain,
including
glioblastoma
neuroinflammation,
face
critical
hurdles
for
efficiently
delivering
entities
owing
BBB.
can
surmount
these
by
utilizing
various
populations,
such
as
stem
cells,
monocytes/macrophages,
neutrophils,
platelets,
potential
functional
carriers
cargo
through
These
carrier
cells
have
innate
capability
traverse
BBB,
transit
brain
parenchyma,
specifically
reach
disease
inflammatory
neoplastic
lesions
chemotactic
navigation,
i.e.,
movement
attributed
chemical
stimuli.
Chemotherapeutic
drugs
delivered
achieve
tumor-specific
targeting
discussed.
This
article
explores
types
TME
with
in-depth
mechanisms
characterization
techniques
decipher
backpack
dissociation
dynamics
(nanoparticle
payload
detachment
characteristics
from
hitchhiked
cells)
challenges
toward
prospective
clinical
translation.
Advances in Colloid and Interface Science,
Год журнала:
2023,
Номер
321, С. 103007 - 103007
Опубликована: Сен. 25, 2023
It
is
well
known
that
metal-organic-framework
(MOF)
nanostructures
have
unique
characteristics
such
as
high
porosity,
large
surface
areas,
and
adjustable
biofunctionalities,
so
they
are
ideal
candidates
for
developing
drug
delivery
systems
(DDSs)
theranostic
platforms
in
cancer
treatment.
Despite
the
number
of
MOF
been
discovered,
conventional
MOF-derived
nanosystems
only
a
single
biofunctional
source
poor
colloidal
stability.
Accordingly,
it
has
demonstrated
core-shell
with
good
stability
useful
method
generating
efficient
delivery,
multimodal
imaging,
synergistic
therapeutic
systems.
The
preparation
done
variety
materials,
but
inorganic
nanoparticles
(NPs)
found
to
be
more
effective
imaging-guided
tumor
Herein,
we
aimed
overview
synthesis
NPs@MOF
followed
by
application
MOFs
derived
from
magnetic,
quantum
dots
(QDs),
gold
(Au),
gadolinium
(Gd)
NPs
Afterwards,
surveyed
different
factors
affecting
prolonged
therapy,
cellular
uptake,
biocompatibility,
biodegradability,
enhanced
permeation
retention
(EPR)
effect
MOFs.
Last
not
least,
discussed
challenges
future
prospects
field.
We
envision
this
article
may
hold
great
promise
providing
valuable
insights
regarding
hybrid
promising
potential
combination
therapy.