Vaccines,
Journal Year:
2020,
Volume and Issue:
8(4), P. 615 - 615
Published: Oct. 17, 2020
One
of
the
principal
goals
cancer
immunotherapy
is
development
efficient
therapeutic
vaccines
that
are
able
to
elicit
an
effector
as
well
memory
T
cell
response
specific
tumor
antigens.
In
recent
years,
attention
has
been
focused
on
personalization
vaccines.
However,
efficacy
still
disappointing
despite
large
number
vaccine
strategies
targeting
different
tumors
have
evaluated
in
years.
While
preclinical
data
frequently
shown
encouraging
results,
clinical
trials
not
provided
satisfactory
date.
The
main
reason
for
such
failures
complexity
identifying
target
antigens
should
be
unique
or
overexpressed
only
by
cells
compared
normal
cells.
Most
included
non-mutated
self-antigens,
eliciting
mainly
with
low-affinity
receptors
(TCR)
unable
mediate
effective
anti-tumor
response.
this
review,
employed
years
described,
along
potential
new
classes
human
endogenous
retroviral
elements
(HERVs),
unconventional
antigens,
and/or
heteroclitic
peptides.
Signal Transduction and Targeted Therapy,
Journal Year:
2023,
Volume and Issue:
8(1)
Published: Jan. 6, 2023
Abstract
Recent
advances
in
neoantigen
research
have
accelerated
the
development
and
regulatory
approval
of
tumor
immunotherapies,
including
cancer
vaccines,
adoptive
cell
therapy
antibody-based
therapies,
especially
for
solid
tumors.
Neoantigens
are
newly
formed
antigens
generated
by
cells
as
a
result
various
tumor-specific
alterations,
such
genomic
mutation,
dysregulated
RNA
splicing,
disordered
post-translational
modification,
integrated
viral
open
reading
frames.
recognized
non-self
trigger
an
immune
response
that
is
not
subject
to
central
peripheral
tolerance.
The
quick
identification
prediction
neoantigens
been
made
possible
advanced
next-generation
sequencing
bioinformatic
technologies.
Compared
tumor-associated
antigens,
highly
immunogenic
provide
emerging
targets
personalized
serve
prospective
predictors
survival
prognosis
checkpoint
blockade
responses.
therapies
will
be
aided
understanding
mechanism
underlying
neoantigen-induced
anti-tumor
streamlining
process
neoantigen-based
immunotherapies.
This
review
provides
overview
on
characterization
outlines
clinical
applications
immunotherapeutic
strategies
based
neoantigens.
We
also
explore
their
current
status,
inherent
challenges,
translation
potential.
Journal of Hematology & Oncology,
Journal Year:
2020,
Volume and Issue:
13(1)
Published: Dec. 1, 2020
Abstract
Over
the
past
few
decades,
RNA
sequencing
has
significantly
progressed,
becoming
a
paramount
approach
for
transcriptome
profiling.
The
revolution
from
bulk
to
single-molecular,
single-cell
and
spatial
approaches
enabled
increasingly
accurate,
individual
cell
resolution
incorporated
with
information.
Cancer,
major
malignant
heterogeneous
lethal
disease,
remains
an
enormous
challenge
in
medical
research
clinical
treatment.
As
vital
tool,
been
utilized
many
aspects
of
cancer
therapy,
including
biomarker
discovery
characterization
heterogeneity
evolution,
drug
resistance,
immune
microenvironment
immunotherapy,
neoantigens
so
on.
In
this
review,
latest
studies
on
technology
their
applications
are
summarized,
future
challenges
opportunities
discussed.
Biomarker Research,
Journal Year:
2020,
Volume and Issue:
8(1)
Published: Aug. 26, 2020
Abstract
Although
the
clinical
development
of
immune
checkpoint
inhibitors
(ICIs)
therapy
has
ushered
in
a
new
era
anti-tumor
therapy,
with
sustained
responses
and
significant
survival
advantages
observed
multiple
tumors,
most
patients
do
not
benefit.
Therefore,
more
attention
been
paid
to
identification
predictive
biomarkers
for
response
ICIs,
in-depth
comprehensive
understanding
continuously
explored
recent
years.
Predictive
markers
ICIs
efficacy
have
gradually
from
expression
intermolecular
interactions
within
tumor
cells
various
molecules
microenvironment,
extended
exploration
circulating
host
systemic
markers.
With
high-throughput
sequencing
microarray
technology,
variety
biomarker
strategies
deeply
achieved
process
single
marker
multifactorial
synergistic
Comprehensive
predictive-models
developed
by
integrating
different
types
data
based
on
components
tumor-host
is
direction
future
research
will
profound
impact
field
precision
immuno-oncology.
In
this
review,
we
analyze
course
progress
as
an
adjunctive
tool
immunotherapy
effectively
identifying
discuss
their
directions
achieving
Frontiers in Immunology,
Journal Year:
2019,
Volume and Issue:
10
Published: Dec. 17, 2019
Immunotherapy
is
often
perceived
as
a
relatively
recent
advance.
In
reality,
however,
one
should
be
looking
for
the
beginnings
of
cancer
immunotherapy
under
different
names
far
in
Antiquity.
The
first
scientific
attempts
to
modulate
patients'
immune
systems
cure
can
attributed
two
German
physicians,
Fehleisen
and
Busch,
who
independently
noticed
significant
tumour
regression
after
erysipelas
infection.
next
advances
came
from
William
Bradley
Coley
known
today
Father
Immunotherapy.
It
was
attempted
harness
system
treating
bone
1891.
His
achievements
were
largely
unnoticed
over
fifty
years,
several
seminal
discoveries
field
Immunology,
such
existence
T
cells
their
crucial
role
immunity
1967,
stepped
up
research
towards
today.
following
paper
tracks
its
until
events,
including
2018
Nobel
Prize
award
James
Allison
Tasuku
Honjo
meticulous
work
on
checkpoint
molecules
potential
therapeutic
targets.
That
has
led
successful
development
new
inhibitors,
CAR
T-cells
oncolytic
viruses
pace
brings
highest
hope
future
treatment.
Cell,
Journal Year:
2020,
Volume and Issue:
182(1), P. 226 - 244.e17
Published: July 1, 2020
Lung
cancer
in
East
Asia
is
characterized
by
a
high
percentage
of
never-smokers,
early
onset
and
predominant
EGFR
mutations.
To
illuminate
the
molecular
phenotype
this
demographically
distinct
disease,
we
performed
deep
comprehensive
proteogenomic
study
on
prospectively
collected
cohort
Taiwan,
representing
stage,
predominantly
female,
non-smoking
lung
adenocarcinoma.
Integrated
genomic,
proteomic,
phosphoproteomic
analysis
delineated
attributes
hallmarks
tumor
progression.
Mutational
signature
revealed
age-
gender-related
mutagenesis
mechanisms,
prevalence
APOBEC
mutational
younger
females
over-representation
environmental
carcinogen-like
signatures
older
females.
A
proteomics-informed
classification
distinguished
clinical
characteristics
stage
patients
with
Furthermore,
integrated
protein
network
cellular
remodeling
underpinning
trajectories
nominated
candidate
biomarkers
for
patient
stratification
therapeutic
intervention.
This
multi-omic
architecture
may
help
develop
strategies
management
never-smoker
Journal of Hematology & Oncology,
Journal Year:
2022,
Volume and Issue:
15(1)
Published: Aug. 17, 2022
Abstract
The
discovery
of
immune
checkpoint
inhibitors
(ICIs)
has
now
been
universally
acknowledged
as
a
significant
breakthrough
in
tumor
therapy
after
the
targeted
treatment
molecules:
anti-programmed
cell
death
protein
1/programmed
ligand
1
(PD-1/PD-L1)
and
anti-cytotoxic
T
lymphocyte-associated
antigen-4
(CTLA-4)
on
several
cancer
types
achieved
satisfying
results.
However,
there
are
still
quite
lot
patients
suffering
from
severe
side
effects
ineffective
outcomes.
Although
current
ICI
is
far
satisfying,
series
novel
molecules
with
remarkable
preclinical
clinical
benefits
being
widely
investigated,
like
V-domain
Ig
suppressor
activation
(VISTA),
which
can
also
be
called
PD-1
homolog
(PD-1H),
ectonucleotidases:
CD39,
CD73,
CD38,
belong
to
ribosyl
cyclase
family,
etc.
In
this
review,
we
systematically
summarized
discussed
these
molecules'
biological
structures,
molecular
features,
corresponding
drugs,
aiming
help
in-depth
understanding
promote
practice
therapy.
Frontiers in Immunology,
Journal Year:
2022,
Volume and Issue:
12
Published: Jan. 7, 2022
In
the
last
decade,
treatment
of
non-small
cell
lung
cancer
(NSCLC)
has
been
revolutionized
by
introduction
immune
checkpoint
inhibitors
(ICI)
directed
against
programmed
death
protein
1
(PD-1)
and
its
ligand
(PD-L1),
or
cytotoxic
T
lymphocyte
antigen
4
(CTLA-4).
spite
these
improvements,
some
patients
do
not
achieve
any
benefit
from
ICI,
inevitably
develop
resistance
to
therapy
over
time.
Tumor
microenvironment
(TME)
might
influence
response
immunotherapy
due
prominent
role
in
multiple
interactions
between
neoplastic
cells
system.
Studies
investigating
perspective
TME
pointed
out
a
complex
scenario
where
tumor
angiogenesis,
soluble
factors,
suppressive/regulatory
elements
composing
itself
participate
growth.
this
review,
we
point
current
state
knowledge
involving
relationship
components
NSCLC
as
well
their
with
providing
an
update
on
novel
predictors
currently
employed
ICI
new
therapeutic
targets
investigational
agents.
first
place,
increasing
evidence
suggests
that
represent
promising
biomarker
sensitivity
based
presence
immune-modulating
cells,
such
Treg,
myeloid
derived
suppressor
associated
macrophages,
which
are
known
induce
immunosuppressive
environment,
poorly
responsive
ICI.
Consequently,
clinical
studies
have
designed
towards
pro-immunogenic
subsequently
improve
activity
Currently,
mostly
approach
relies
association
“classic”
targeting
PD-1/PD-L1
agents
molecules,
LAG-3
TIM-3.
To
date,
trials
already
shown
results,
while
multitude
prospective
ongoing,
results
significantly
future
immunotherapy.
Frontiers in Immunology,
Journal Year:
2021,
Volume and Issue:
12
Published: Feb. 23, 2021
The
past
decade
has
witnessed
groundbreaking
advances
in
the
field
of
microbiome
research.
An
area
where
immense
implications
have
been
demonstrated
is
tumor
biology.
affects
initiation
and
progression
through
direct
effects
on
cells
indirectly
manipulation
immune
system.
It
can
also
determine
response
to
cancer
therapies
predict
disease
survival.
Modulation
be
harnessed
potentiate
efficacy
immunotherapies
decrease
their
toxicity.
In
this
review,
we
comprehensively
dissect
recent
evidence
regarding
interaction
anti-tumor
machinery
outline
critical
questions
which
need
addressed
as
further
explore
dynamic
colloquy.