International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(3), P. 1737 - 1737
Published: Feb. 1, 2024
The
advent
of
immune
checkpoint
inhibitors
(ICIs)
has
represented
a
breakthrough
in
the
treatment
many
cancers,
although
high
number
patients
fail
to
respond
ICIs,
which
is
partially
due
ability
tumor
cells
evade
system
surveillance.
Non-coding
microRNAs
(miRNAs)
have
been
shown
modulate
evasion
cells,
and
there
thus
growing
interest
elucidating
whether
these
miRNAs
could
be
targetable
or
proposed
as
novel
biomarkers
for
prognosis
response
ICIs.
We
therefore
performed
an
extensive
literature
analysis
evaluate
clinical
utility
with
confirmed
direct
relationship
As
result
this
systematic
review,
we
stratified
miRNA
landscape
into
(i)
whose
levels
directly
(ii)
expression
modulated
by
(iii)
that
elicit
toxic
effects
participate
immune-related
adverse
events
(irAEs)
caused
Biomarker Research,
Journal Year:
2024,
Volume and Issue:
12(1)
Published: Jan. 17, 2024
Abstract
Immune
checkpoints
play
a
critical
role
in
maintaining
the
delicate
balance
of
immune
activation
order
to
prevent
potential
harm
caused
by
excessive
activation,
autoimmunity,
or
tissue
damage.
B
and
T
lymphocyte
attenuator
(BTLA)
is
one
crucial
checkpoint,
regulating
stimulatory
inhibitory
signals
responses.
Its
interaction
with
herpes
virus
entry
mediator
(HVEM)
plays
an
essential
negatively
responses,
thereby
preserving
homeostasis.
In
cancer,
abnormal
cells
evade
surveillance
exploiting
like
BTLA.
Upregulated
BTLA
expression
linked
impaired
anti-tumor
immunity
unfavorable
disease
outcomes.
preclinical
studies,
BTLA-targeted
therapies
have
shown
improved
treatment
outcomes
enhanced
antitumor
immunity.
This
review
aims
provide
in-depth
understanding
BTLA’s
biology,
its
various
cancers,
as
prognostic
factor.
Additionally,
it
explores
latest
research
on
blockade
cancer
immunotherapy,
offering
hope
for
more
effective
treatments.
Biomedicines,
Journal Year:
2024,
Volume and Issue:
12(1), P. 217 - 217
Published: Jan. 18, 2024
Immunotherapy
is
now
established
as
a
potent
therapeutic
paradigm
engendering
antitumor
immune
response
against
wide
range
of
malignancies
and
other
diseases
by
modulating
the
system
either
through
stimulation
or
suppression
components
such
CD4+
T
cells,
CD8+
B
monocytes,
macrophages,
dendritic
natural
killer
cells.
By
targeting
several
checkpoint
inhibitors
blockers
(e.g.,
PD-1,
PD-L1,
PD-L2,
CTLA-4,
LAG3,
TIM-3)
expressed
on
surface
monoclonal
antibodies
polyclonal
have
been
developed
already
translated
clinically.
In
addition,
cell-based,
CAR
cell
therapies
also
shown
to
be
promising
effective
immunotherapeutic
approaches.
particular,
therapy
has
benefited
from
advancements
in
CRISPR-Cas9
genome
editing
technology,
allowing
generation
modified
cells
with
enhanced
immunity.
However,
emerging
SARS-CoV-2
infection
could
hijack
patient’s
releasing
pro-inflammatory
interleukins
cytokines
IL-1β,
IL-2,
IL-6,
IL-10,
IFN-γ
TNF-α,
respectively,
which
can
further
promote
neutrophil
extravasation
vasodilation
blood
vessels.
Despite
significant
development
advanced
technologies,
after
certain
period
treatment,
cancer
relapses
due
resistance
immunotherapy.
Resistance
may
primary
(where
tumor
do
not
respond
treatment),
secondary
acquired
develop
gradually
ICIs
therapy).
this
context,
review
aims
address
existing
technologies
mechanisms
drugs,
explain
impact
COVID-19
treatment.
we
will
discuss
what
future
implementation
these
strategies
drug
resistance.
Finally,
emphasize
practical
steps
lay
groundwork
for
enlightened
policy
intervention
resource
allocation
care
patients.
Frontiers in Immunology,
Journal Year:
2022,
Volume and Issue:
13
Published: Oct. 5, 2022
The
tumor
microenvironment
(TME)
is
a
significant
contributor
to
cancer
progression
containing
complex
connections
between
cellular
and
chemical
components
provides
suitable
substrate
for
growth
development.
Growing
evidence
shows
targeting
cells
while
ignoring
the
surrounding
TME
not
effective
enough
overcome
disease.
Fibroblasts
are
essential
sentinels
of
stroma
that
due
certain
conditions
in
TME,
such
as
oxidative
stress
local
hypoxia,
become
activated,
play
prominent
role
physical
support
enhancement
tumorigenesis.
Activated
fibroblasts
defined
cancer-associated
(CAFs),
crucial
regulating
biological
behavior
tumors,
metastasis
drug
resistance.
CAFs
highly
heterogeneous
populations
have
different
origins
and,
addition
their
supporting
stromal
cells,
multiple
immunosuppressive
functions
via
membrane
secretory
patterns.
secretion
cytokines/chemokines,
interactions
mediate
recruitment
regulatory
immune
reprogramming
an
function
immature
myeloid
just
few
examples
how
contribute
escape
tumors
through
various
direct
indirect
mechanisms
on
specific
cell
populations.
Moreover,
directly
abolish
cytotoxic
lymphocytes.
activation
overexpression
inhibitory
checkpoints
(iICPs)
or
ligands
compartments
one
main
inactivate
tumor-infiltrating
lymphocytes
lesions.
also
players
induction
expression
iICPs
suppression
response
TME.
Based
available
studies,
CAF
subsets
could
modulate
two
ways;
by
activated
production
soluble
then
upregulation
With
focus
CAFs'
roles
well
use
immunotherapy
diagnostics,
we
present
evolving
understanding
mechanism
this
review.
Understanding
complete
picture
will
help
develop
new
strategies
improve
precision
therapy.
Cancers,
Journal Year:
2022,
Volume and Issue:
14(7), P. 1710 - 1710
Published: March 28, 2022
The
approval
of
immune
checkpoint
inhibitors
(ICI)
that
serve
to
enhance
effector
T-cell
anti-tumor
responses
has
strongly
improved
success
rates
in
the
treatment
metastatic
melanoma
and
other
tumor
types.
currently
approved
ICI
constitute
monoclonal
antibodies
blocking
cytotoxic
T-lymphocyte-associated
protein
(CTLA)-4
anti-programmed
cell
death
(PD)-1.
By
this,
T-cell-inhibitory
CTLA-4/CD80/86
PD-1/PD-1L/2L
signaling
axes
are
inhibited.
This
leads
sustained
activity
circumvents
evasion
cells,
which
frequently
upregulate
PD-L1
expression
modulate
molecule
on
leukocytes.
As
a
result,
profound
clinical
observed
40–60%
patients.
Despite
pivotal
role
T
cells
for
triggering
immunity,
mounting
evidence
indicates
efficacy
may
also
be
attributable
types
than
cells.
In
particular,
emerging
research
shown
impacts
innate
such
as
myeloid
natural
killer
lymphoid
amplify
tumoricidal
functions
beyond
thus
improves
efficacy.
Effects
non-T
additionally
explain,
part,
character
extent
adverse
effects
associated
with
treatment.
Deeper
knowledge
these
is
required
further
develop
terms
responsiveness
patients
treatment,
overcome
resistance
alleviate
effects.
this
review
we
give
an
overview
into
known
immunomodulatory
compartment.
BMC Cancer,
Journal Year:
2023,
Volume and Issue:
23(1)
Published: Jan. 30, 2023
CD276
(also
known
as
B7-H3)
is
one
of
the
most
important
immune
checkpoints
CD28
and
B7
superfamily,
its
abnormal
expression
closely
associated
with
various
types
cancer.
It
has
been
shown
that
able
to
inhibit
function
T
cells,
this
gene
may
potentially
be
a
promising
immunotherapy
target
for
different
cancer.Since
few
systematic
studies
have
published
on
role
in
cancer
date,
present
study
employed
single-cell
sequencing
bioinformatics
methods
analyze
patterns,
clinical
significance,
prognostic
value,
epigenetic
alterations,
DNA
methylation
level,
tumor
cell
infiltration
functions
In
order
potential
underlying
mechanism
glioblastoma
(GBM)
assess
LinkedOmics
database
was
used
explore
biological
co-expression
pattern
GBM,
Gene
Ontology
(GO)
Kyoto
Encyclopedia
Genes
Genomes
(KEGG)
enrichment
analyses
were
performed.
addition,
simple
validation
above
performed
using
reverse
transcription-quantitative
(RT-q)PCR
assay.The
results
revealed
highly
expressed,
often
poorer
survival
prognosis,
majority
found
infiltration,
checkpoint
genes
immunoregulatory
interactions
between
lymphoid
non-lymphoid
cell.
also
network
exerts
wide
influence
activation
GBM.
The
positively
correlated
neutrophil-mediated
immunity,
although
it
negatively
level
neurotransmitters,
neurotransmitter
transport
regulation
neuropeptide
signaling
pathways
noteworthy
significantly
higher
GBM
compared
normal
controls
according
RT-qPCR
analysis,
network,
chemotherapeutic
drug
sensitivity
further
explored.
conclusion,
findings
strongly
expressed
poor
prognosis
cancer,
including
T-cell
genes,
immunomodulatory
lymphocytes
cells.Taken
together,
based
our
roles
cancers,
especially
serve
biomarker
Immunology,
Journal Year:
2023,
Volume and Issue:
169(4), P. 389 - 399
Published: March 1, 2023
Abstract
Despite
the
clinical
success
of
monoclonal
and
bispecific
antibodies,
there
are
still
limitations
in
therapeutic
effect
malignant
tumours,
such
as
low
response
rate,
treatment
resistance,
so
on,
inspiring
exploration
trispecific
antibodies
(TsAbs).
TsAbs
further
improve
safety
efficacy
has
great
potential
through
three
targets
combination
formats
optimization.
This
article
reviews
development
history
target
features
TsAbs.
Although
challenges
application
TsAbs,
it
is
undeniable
that
may
be
a
breakthrough
antibody
drugs.
Frontiers in Oncology,
Journal Year:
2024,
Volume and Issue:
14
Published: Feb. 7, 2024
Cryoablation,
as
a
minimally
invasive
technology
for
the
treatment
of
tumors,
destroys
target
tumors
with
lethal
low
temperatures.
It
simultaneously
releases
large
number
tumor-specific
antigens,
pro-inflammatory
cytokines,
and
nucleoproteins,
known
“danger
signals”,
activating
body’s
innate
adaptive
immune
responses.
However,
tumor
cells
can
promote
inactivation
effector
by
reprogramming
checkpoints,
leading
to
insufficiency
these
antigens
induce
an
response
capable
eradicating
tumor.
Immune
checkpoint
blockers
rejuvenate
exhausted
T
blocking
checkpoints
that
programmed
death
cells,
are
therefore
considered
promising
therapeutic
strategy
enhance
effects
cryoablation.
In
this
review,
we
provide
detailed
explanation
immunological
mechanisms
cryoablation
articulate
theoretical
basis
research
progress
cancer
combined
blockers.
Preliminary
data
indicates
exhibits
good
synergy
has
been
proven
be
safe
effective.