Theranostics,
Journal Year:
2019,
Volume and Issue:
9(25), P. 7759 - 7771
Published: Jan. 1, 2019
Cancer
immunotherapy
modulates
and
leverages
the
host
immune
system
to
treat
cancer.
The
past
decade
has
witnessed
historical
advancement
of
cancer
immunotherapy.
A
myriad
approaches
have
been
explored
elicit
or
augment
anticancer
innate
immunity
and/or
adaptive
immunity.
Recently,
activation
stimulator
interferon
(IFN)
genes
(STING),
an
intracellular
receptor
residing
in
endoplasmic
reticulum,
shown
great
potential
enhance
antitumor
through
induction
a
variety
pro-inflammatory
cytokines
chemokines,
including
type
I
IFNs.
number
natural
synthetic
STING
agonists
discovered
developed,
tested
preclinical
models
clinic
for
diseases
such
as
infectious
diseases.
Cyclic
dinucleotides
(CDNs),
cyclic
dimeric
guanosine
monophosphate
(c-di-GMP),
adenosine
(c-di-AMP),
GMP-AMP
(cGAMP),
are
class
that
can
responses.
However,
CDNs
hydrophilic
small
molecules
with
negative
charges
susceptible
enzymatic
degradation,
leading
low
bioavailability
target
tissues
yet
unwanted
toxicities
narrow
therapeutic
windows.
Drug
delivery
systems,
coupled
nucleic
acid
chemistry,
exploited
address
these
challenges.
Here,
we
will
discuss
underlying
immunological
mechanisms
activation,
focus
on
agonists,
ACS Nano,
Journal Year:
2017,
Volume and Issue:
11(10), P. 9594 - 9613
Published: Sept. 19, 2017
The
interface
of
bio–nano
science
and
cancer
medicine
is
an
area
experiencing
much
progress
but
also
beset
with
controversy.
Core
concepts
the
field—e.g.,
enhanced
permeability
retention
(EPR)
effect,
tumor
targeting
accumulation,
even
purpose
"nano"
in
medicine—are
hotly
debated.
In
parallel,
considerable
advances
neighboring
fields
are
occurring
rapidly,
including
recent
"immuno-oncology"
fundamental
impact
it
having
on
our
understanding
clinical
treatment
group
diseases
collectively
known
as
cancer.
Herein,
we
(i)
revisit
how
commonly
treated
clinic
this
relates
to
nanomedicine;
(ii)
examine
ongoing
debate
relevance
EPR
effect
targeting;
(iii)
highlight
ways
improve
next-generation
nanomedicines;
(iv)
discuss
emerging
concept
working
(and
not
against)
biology.
While
discussing
these
controversies,
challenges,
concepts,
opportunities,
explore
new
directions
for
field
nanomedicine.
Advanced Science,
Journal Year:
2019,
Volume and Issue:
6(17)
Published: June 21, 2019
Abstract
Immunotherapy
has
emerged
as
an
effective
strategy
for
the
prevention
and
treatment
of
a
variety
diseases,
including
cancer,
infectious
inflammatory
autoimmune
diseases.
Immunomodulatory
nanosystems
can
readily
improve
therapeutic
effects
simultaneously
overcome
many
obstacles
facing
method,
such
inadequate
immune
stimulation,
off‐target
side
effects,
bioactivity
loss
agents
during
circulation.
In
recent
years,
researchers
have
continuously
developed
nanomaterials
with
new
structures,
properties,
functions.
This
Review
provides
most
advances
nanotechnology
immunostimulation
immunosuppression.
cancer
immunotherapy,
play
essential
role
in
cell
activation
tumor
microenvironment
modulation,
well
combination
other
antitumor
approaches.
encouraging
outcomes
from
using
nanomaterial
vaccines
against
viral
bacterial
infections
been
reported.
addition,
nanoparticles
also
potentiate
immunosuppressive
cells
Finally,
challenges
prospects
applying
to
modulate
immunotherapy
are
discussed.
Advanced Materials,
Journal Year:
2018,
Volume and Issue:
30(22)
Published: March 26, 2018
Abstract
White
blood
cells
(WBCs)
are
a
major
component
of
immunity
in
response
to
pathogen
invasion.
Neutrophils
the
most
abundant
WBCs
humans,
playing
central
role
acute
inflammation
induced
by
pathogens.
Adhesion
vasculature
and
tissue
infiltration
neutrophils
key
processes
inflammation.
Many
inflammatory/autoimmune
disorders
cancer
therapies
have
been
found
be
involved
activation
neutrophils.
A
promising
strategy
develop
novel
targeted
drug
delivery
systems
is
targeting
exploitation
activated
Herein,
new
platform
based
on
reviewed.
There
two
types
systems:
as
carriers
neutrophil‐membrane‐derived
nanovesicles.
It
discussed
how
nanoparticles
hijack
vivo
deliver
therapeutics
across
vessel
barriers
nanovesicles
target
inflamed
vasculature.
Finally,
potential
applications
neutrophil‐based
treating
cancers
presented.
Science Advances,
Journal Year:
2019,
Volume and Issue:
5(10)
Published: Oct. 11, 2019
Erythrocytes
or
red
blood
cells
(RBCs)
represent
a
promising
cell-mediated
drug
delivery
platform
due
to
their
inherent
biocompatibility.
Here,
we
developed
an
antigen
system
based
on
the
nanoerythrosomes
derived
from
RBCs,
inspired
by
splenic
antigen-presenting
cell
targeting
capacity
of
senescent
RBCs.
Tumor
antigens
were
loaded
onto
fusing
tumor
membrane-associated
with
nanoerythrosomes.
This
antigen-loaded
(nano-Ag@erythrosome)
elicited
responses
in
vivo
and,
combination
anti-programmed
death
ligand
1
(PD-L1)
blockade,
inhibited
growth
B16F10
and
4T1
models.
We
also
generated
model
showing
that
"personalized
nano-Ag@erythrosomes"
could
be
achieved
RBCs
surgically
removed
tumors,
which
effectively
reduced
recurrence
metastasis
after
surgery.
Advanced Science,
Journal Year:
2019,
Volume and Issue:
6(10)
Published: March 13, 2019
Combined
phototherapy
and
immunotherapy
demonstrates
strong
potential
in
the
treatment
of
metastatic
cancers.
An
upconversion
nanoparticle
(UCNP)
based
antigen-capturing
nanoplatform
is
designed
to
synergize
phototherapies
immunotherapy.
In
particular,
this
constructed
via
self-assembly
DSPE-PEG-maleimide
indocyanine
green
(ICG)
onto
UCNPs,
followed
by
loading
photosensitizer
rose
bengal
(RB).
ICG
significantly
enhances
RB-based
photodynamic
therapy
efficiency
UCNP/ICG/RB-mal
upon
activation
a
near-infrared
(NIR)
laser,
simultaneously
achieving
selective
photothermal
therapy.
Most
importantly,
tumor-derived
protein
antigens,
arising
from
phototherapy-treated
tumor
cells,
can
be
captured
retained
situ,
due
functionality
maleimide,
which
further
enhance
antigen
uptake
presentation
antigen-presenting
cells.
The
synergized
photothermal,
photodynamic,
immunological
effects
using
light-activated
induces
tumor-specific
immune
response.
experiments,
intratumoral
administration
UCNP/ICG/RB-mal,
noninvasive
irradiation
with
an
NIR
destroys
primary
tumors
inhibits
untreated
distant
tumors,
poorly
immunogenic,
highly
4T1
mammary
model.
With
simultaneous
use
anti-CTLA-4,
about
84%
treated
tumor-bearing
mice
achieve
long-term
survival
34%
develop
immunity.
Overall,
provides
promising
approach
for
Advanced Materials,
Journal Year:
2019,
Volume and Issue:
31(19)
Published: March 18, 2019
Abstract
Advances
in
the
field
of
nanotechnology
together
with
an
increase
understanding
tumor
immunology
have
paved
way
for
development
more
personalized
cancer
immuno‐nanomedicines.
Nanovehicles,
due
to
their
specific
physicochemical
properties,
are
emerging
as
key
translational
moieties
tackling
tumor‐promoting,
M2‐like
tumor‐associated
macrophages
(TAMs).
Cancer
immuno‐nanomedicines
target
TAMs
primarily
by
blocking
TAM
survival
or
affecting
signaling
cascades,
restricting
macrophage
recruitment
tumors
and
re‐educating
tumor‐promoting
tumoricidal,
M1‐like
phenotype.
Here,
effector
mechanisms
strategies
targeting
summarized,
followed
a
focus
on
mechanistic
considerations
novel
Furthermore,
imaging
nanoparticles
so
forecast
patient's
clinical
outcome,
describing
treatment
options,
observing
therapy
responses
is
also
discussed.
At
present,
that
being
investigated
not
only
at
basic
research
level
but
early
trials.
The
significance
TAM‐targeting
biomaterials
highlighted,
goal
facilitating
future
translation.
Advanced Materials,
Journal Year:
2019,
Volume and Issue:
31(34)
Published: Feb. 18, 2019
Cancer
immunotherapies
that
harness
the
body's
immune
system
to
combat
tumors
have
received
extensive
attention
and
become
mainstream
strategies
for
treating
cancer.
Despite
promising
results,
some
problems
remain,
such
as
limited
patient
response
rate
emergence
of
severe
immune-related
adverse
effects.
For
most
patients,
therapeutic
efficacy
cancer
immunotherapy
is
mainly
by
immunosuppressive
tumor
microenvironment
(TME).
To
overcome
obstacles
in
TME,
immunomodulation
factors
cells
(e.g.,
T
antigen-presenting
cells)
should
be
carefully
designed
evaluated.
Nanoengineered
synthetic
niches
emerged
highly
customizable
platforms
with
a
potent
capability
reprogramming
TME.
Here,
recent
developments
nano-biomaterials
are
rationally
modulate
TME
spatiotemporal
manner
enhanced
which
highlighted.
Chemical Society Reviews,
Journal Year:
2019,
Volume and Issue:
48(22), P. 5506 - 5526
Published: Jan. 1, 2019
Cancer
immunotherapy
by
educating
or
stimulating
patients'
own
immune
systems
to
attack
cancer
cells
has
demonstrated
promising
therapeutic
responses
in
the
clinic.
However,
although
number
of
approved
immunotherapeutics
is
rapidly
increasing,
key
challenges
such
as
limited
clinical
response
rate
and
significant
autoimmunity-related
adverse
effects
remain
be
resolved.
Recently,
it
been
discovered
that
a
diverse
range
biomaterials-assisted
local
treatment
methods
including
localized
radiotherapy,
chemotherapy
phototherapy
are
able
stimulate
systems,
often
inducing
immunogenic
cell
death
(ICD).
The
triggered
tumor-specific
immunological
after
treatments,
especially
combination
with
checkpoint
blockade
(ICB)
therapy,
can
achieve
abscopal
effect
whole-body
spreading
metastatic
cells,
later
on
result
memory
inhibit
tumor
recurrence.
Moreover,
delivery
immunomodulatory
therapeutics
biomaterials
also
an
alternative
strategy
improve
reduce
side
immunotherapy.
In
this
review,
we
would
like
summarize
latest
advances,
opportunities
utilizing
strategies
for
enhancing
anticancer
immunity,
discuss
further
prospects
field
together
how
may
possibly
translated
into
use.