Cancers,
Journal Year:
2022,
Volume and Issue:
14(18), P. 4344 - 4344
Published: Sept. 6, 2022
In
the
last
decade,
tumor-infiltrating
lymphocytes
(TILs)
have
been
recognized
as
clinically
relevant
prognostic
markers
for
improved
survival,
providing
immunological
basis
development
of
new
therapeutic
strategies
and
showing
a
significant
predictive
role
in
several
malignancies,
including
ovarian
cancer
(OC).
fact,
many
OCs
show
TILs
whose
typology
degree
infiltration
shown
to
be
strongly
correlated
with
prognosis
survival.
The
OC
histological
subtype
higher
presence
is
high-grade
serous
carcinoma
(HGSC)
followed
by
endometrioid
subtype,
whereas
mucinous
clear
cell
seem
contain
lower
percentage
TILs.
abundant
suggests
an
immunogenic
potential
this
tumor.
Despite
high
potential,
has
described
highly
immunosuppressive
tumor
expression
PD1
Although
further
studies
are
needed
better
define
their
stratification
implication,
intraepithelial
represent
factor
take
into
account
OC.
review,
we
will
discuss
promising
which
able
reflect
anticancer
immune
response,
describing
capability
predict
therapy
response
International Journal of Molecular Sciences,
Journal Year:
2021,
Volume and Issue:
22(12), P. 6532 - 6532
Published: June 18, 2021
Ovarian
cancer
response
to
immunotherapy
is
limited;
however,
the
evaluation
of
sensitive/resistant
target
treatment
subpopulations
based
on
stratification
by
tumor
biomarkers
may
improve
predictiveness
immunotherapy.
These
markers
include
mutation
burden,
PD-L1,
tumor-infiltrating
lymphocytes,
homologous
recombination
deficiency,
and
neoantigen
intratumoral
heterogeneity.
Future
directions
in
ovarian
utilization
these
select
ideal
candidates.
This
paper
reviews
role
as
well
novel
therapeutics
study
designs
involving
that
increase
likelihood
success
with
cancer.
British Journal of Cancer,
Journal Year:
2021,
Volume and Issue:
124(11), P. 1759 - 1776
Published: March 29, 2021
Abstract
Cancer
is
a
leading
cause
of
death
worldwide
and,
despite
new
targeted
therapies
and
immunotherapies,
many
patients
with
advanced-stage-
or
high-risk
cancers
still
die,
owing
to
metastatic
disease.
Adoptive
T-cell
therapy,
involving
the
autologous
allogeneic
transplant
tumour-infiltrating
lymphocytes
genetically
modified
T
cells
expressing
novel
receptors
chimeric
antigen
receptors,
has
shown
promise
in
treatment
cancer
patients,
durable
responses
some
cases,
cure.
Technological
advances
genomics,
computational
biology,
immunology
cell
manufacturing
have
brought
aspiration
individualised
for
closer
reality.
This
era
cell-based
therapeutics
challenges
traditional
standards
therapeutic
interventions
provides
opportunities
paradigm
shift
our
approach
therapy.
Invited
speakers
at
2020
symposium
discussed
three
areas—cancer
cell-therapy
manufacturing—that
are
essential
effective
translation
solid
malignancies.
Key
been
made
understanding
genetic
intratumour
heterogeneity,
strategies
accurately
identify
neoantigens,
overcome
exhaustion
circumvent
tumour
immunosuppression
after
infusion
being
developed.
Advances
cell-manufacturing
approaches
that
potential
establish
cell-therapies
as
credible
options.
face
but
hold
great
improving
clinical
outcomes
tumours.
Cancer Cell International,
Journal Year:
2022,
Volume and Issue:
22(1)
Published: Jan. 3, 2022
Abstract
Recently,
immune
checkpoint
inhibitors
(ICIs)
therapy
has
become
a
promising
therapeutic
strategy
with
encouraging
outcomes
due
to
their
durable
anti-tumor
effects.
Though,
tumor
inherent
or
acquired
resistance
ICIs
accompanied
treatment-related
toxicities
hamper
clinical
utility.
Overall,
about
60–70%
of
patients
(e.g.,
melanoma
and
lung
cancer)
who
received
show
no
objective
response
intervention.
The
mainly
caused
by
alterations
in
the
microenvironment
(TME),
which
turn,
supports
angiogenesis
also
blocks
cell
antitumor
activities,
facilitating
cells'
evasion
from
host
immunosurveillance.
Thereby,
it
been
supposed
validated
that
combination
other
means,
ranging
chemoradiotherapy
targeted
therapies
as
well
cancer
vaccines,
can
capably
compromise
blocked
therapy.
Herein,
we
have
focused
on
benefits
groundbreaking
approach
context
immunotherapy
deliver
an
overview
concerning
influences
addition
modalities
circumvent
ICIs.
International Journal of Molecular Sciences,
Journal Year:
2020,
Volume and Issue:
21(23), P. 8984 - 8984
Published: Nov. 26, 2020
Melanoma
is
the
most
aggressive
and
dangerous
form
of
skin
cancer
that
develops
from
transformed
melanocytes.
It
crucial
to
identify
melanoma
at
its
early
stages,
in
situ,
as
it
"curable"
this
stage.
However,
after
metastasis,
difficult
treat
five-year
survival
only
25%.
In
recent
years,
a
better
understanding
etiology
progression
has
made
possible
for
development
targeted
therapeutics,
such
vemurafenib
immunotherapies,
advanced
melanomas.
review,
we
focus
on
molecular
mechanisms
mediate
progression,
with
special
immune
evasion
strategies
utilized
by
melanomas,
evade
host
surveillances.
The
proposed
mechanism
action
roles
immunotherapeutic
agents,
ipilimumab,
nivolumab,
pembrolizumab,
atezolizumab,
adoptive
T-
cell
therapy
plus
T-VEC
treatment
are
discussed.
implore
steps
onset
exploited
these
tumor
cells,
identification
biomarkers
predict
response
critical
design
improved
improve
clinical
outcomes
patients
deadly
disease.
Cancers,
Journal Year:
2022,
Volume and Issue:
14(17), P. 4160 - 4160
Published: Aug. 27, 2022
Over
the
past
decade,
immunotherapy,
especially
cell-based
has
provided
new
strategies
for
cancer
therapy.
Recent
clinical
studies
demonstrated
that
adopting
cell
transfer
of
tumor-infiltrating
lymphocytes
(TILs)
advanced
solid
tumors
showed
good
efficacy.
TIL
therapy
is
a
type
immunotherapy
using
patient’s
own
immune
cells
from
microenvironment
tumor
to
kill
cells.
In
this
review,
we
provide
comprehensive
summary
current
and
challenges
in
isolation
generation.
Moreover,
experience
summarized
discussed,
with
an
emphasis
on
lymphodepletion
regimen,
use
interleukin-2,
related
toxicity.
Furthermore,
highlight
trials
where
used
independently
combination
other
types
cancers.
Finally,
limitations,
future
potential,
directions
treatment
are
also
discussed.
Frontiers in Immunology,
Journal Year:
2022,
Volume and Issue:
13
Published: Oct. 28, 2022
Tumor-infiltrating
lymphocytes
(TILs),
frontline
soldiers
of
the
adaptive
immune
system,
are
recruited
into
tumor
site
to
fight
against
tumors.
However,
their
small
number
and
reduced
activity
limit
ability
overcome
tumor.
Enhancement
TILs
tumors
has
been
interest
for
a
long
time.
A
lack
knowledge
about
microenvironment
(TME)
limited
success
in
primary
TIL
therapies.
Although
advent
engineered
T
cells
revolutionized
immunotherapy
methods
hematologic
cancers,
heterogeneity
solid
warrants
application
with
wide
range
specificity.
Recent
advances
understanding
TME,
exhaustion,
checkpoints
have
paved
way
therapy
regimens.
Nowadays,
regained
attention
as
safe
personalized
immunotherapy,
currently,
several
clinical
trials
evaluating
efficacy
patients
who
failed
conventional
immunotherapies.
Gaining
favorable
outcomes
following
metastatic
melanoma,
cervical
cancer,
ovarian
breast
cancer
raised
hope
refractory
tumors,
too.
Nevertheless,
procedures
face
challenges,
such
high
cost,
timely
expansion,
technical
challenges
selecting
activating
cells.
Herein,
we
reviewed
recent
discussed
perspectives.
Nature Communications,
Journal Year:
2023,
Volume and Issue:
14(1)
Published: March 27, 2023
Profiling
tumors
at
single-cell
resolution
provides
an
opportunity
to
understand
complexities
underpinning
lymph-node
metastases
in
head
and
neck
squamous-cell
carcinoma.
Single-cell
RNAseq
(scRNAseq)
analysis
of
cancer-cell
trajectories
identifies
a
subpopulation
pre-metastatic
cells,
driven
by
actionable
pathways
including
AXL
AURK.
Blocking
these
two
proteins
blunts
tumor
invasion
patient-derived
cultures.
Furthermore,
scRNAseq
analyses
tumor-infiltrating
CD8
+
T-lymphocytes
show
distinct
T-cell
dysfunction,
corroborated
their
clonal
architecture
based
on
receptor
sequencing.
By
determining
key
modulators
trajectories,
followed
validation
using
external
datasets
functional
experiments,
we
uncover
role
for
SOX4
mediating
exhaustion.
Finally,
interactome
between
cells
putative
the
Midkine
pathway
immune-modulation
this
is
confirmed
from
humanized
mice.
Aside
specific
findings,
study
demonstrates
importance
heterogeneity
identifying
vulnerabilities
during
early
metastasis.
Frontiers in Oncology,
Journal Year:
2024,
Volume and Issue:
14
Published: March 20, 2024
Immune
checkpoint
molecules
are
a
group
of
expressed
on
the
surface
immune
cells
that
primarily
regulate
their
homeostasis.
Chimeric
antigen
receptor
(CAR)
T
cell
therapy
is
an
immunotherapeutic
technology
realizes
tumor-targeted
killing
by
constructing
synthetic
expressing
specific
antigens
through
biotechnology.
Currently,
CAR-T
has
achieved
good
efficacy
in
non-solid
tumors,
but
its
treatment
solid
tumors
not
yielded
desired
results.
inhibitors
(ICIs)
combined
with
novel
combination
high
expectations
to
defeat
tumors.
This
review
addresses
challenges
and
this