Cancer Biology and Medicine,
Journal Year:
2023,
Volume and Issue:
unknown, P. 1 - 26
Published: Nov. 24, 2023
In
oncolytic
virus
(OV)
therapy,
a
critical
component
of
tumor
immunotherapy,
viruses
selectively
infect,
replicate
within,
and
eventually
destroy
cells.
Simultaneously,
this
therapy
activates
immune
responses
mobilizes
cells,
thereby
eliminating
residual
or
distant
cancer
However,
because
OVs'
high
immunogenicity
clearance
during
circulation,
their
clinical
applications
are
currently
limited
to
intratumoral
injections,
use
is
severely
restricted.
recent
years,
numerous
studies
have
used
nanomaterials
modify
OVs
decrease
virulence
increase
safety
for
intravenous
injection.
The
most
commonly
modifying
liposomes,
polymers,
albumin,
biosafety,
practicability,
effectiveness.
aim
review
summarize
progress
in
the
these
preclinical
experiments
discuss
challenges
encountered
from
basic
research
application.
Journal of Experimental & Clinical Cancer Research,
Journal Year:
2022,
Volume and Issue:
41(1)
Published: April 15, 2022
Abstract
Glioblastoma
(GBM)
is
the
most
common
high-grade
primary
malignant
brain
tumor
with
an
extremely
poor
prognosis.
Given
survival
currently
approved
treatments
for
GBM,
new
therapeutic
strategies
are
urgently
needed.
Advances
in
decades
of
investment
basic
science
glioblastoma
rapidly
translated
into
innovative
clinical
trials,
utilizing
improved
genetic
and
epigenetic
profiling
as
well
microenvironment
immune
system
interactions.
Following
these
encouraging
findings,
immunotherapy
including
checkpoint
blockade,
chimeric
antigen
receptor
T
(CAR
T)
cell
therapy,
oncolytic
virotherapy,
vaccine
therapy
have
offered
hope
improving
GBM
outcomes;
ongoing
studies
using
combinatorial
therapies
aim
minimizing
adverse
side-effects
augmenting
antitumor
responses.
In
addition,
techniques
to
overcome
blood-brain
barrier
(BBB)
targeted
delivery
being
tested
trials
patients
recurrent
GBM.
Here,
we
set
forth
rationales
promising
treating
review
potential
novel
agents,
current
status
preclinical
discuss
challenges
future
perspectives
immuno-oncology.
Journal of Hematology & Oncology,
Journal Year:
2023,
Volume and Issue:
16(1)
Published: Feb. 8, 2023
RIG-I-like
receptors
(RLRs)
are
intracellular
pattern
recognition
that
detect
viral
or
bacterial
infection
and
induce
host
innate
immune
responses.
The
RLRs
family
comprises
retinoic
acid-inducible
gene
1
(RIG-I),
melanoma
differentiation-associated
5
(MDA5)
laboratory
of
genetics
physiology
2
(LGP2)
have
distinctive
features.
These
not
only
recognize
RNA
intermediates
from
viruses
bacteria,
but
also
interact
with
endogenous
such
as
the
mislocalized
mitochondrial
RNA,
aberrantly
reactivated
repetitive
transposable
elements
in
human
genome.
Evasion
RLRs-mediated
response
may
lead
to
sustained
infection,
defective
immunity
carcinogenesis.
Therapeutic
targeting
provoke
anti-infection
effects,
anticancer
sensitize
"immune-cold"
tumors
checkpoint
blockade.
In
this
review,
we
summarize
current
knowledge
signaling
discuss
rationale
for
therapeutic
cancer.
We
describe
how
can
be
activated
by
synthetic
oncolytic
viruses,
mimicry
radio-chemotherapy,
agonists
systemically
delivered
vivo.
integration
agonism
interference
CAR-T
cells
provides
new
dimensions
complement
cancer
immunotherapy.
Moreover,
update
progress
recent
clinical
trials
therapy
involving
activation
modulation.
Further
studies
mechanisms
underlying
will
shed
light
on
development
therapeutics.
Manipulation
represents
an
opportunity
clinically
relevant
therapy.
Addressing
challenges
field
help
develop
future
generations
Molecular Cancer,
Journal Year:
2022,
Volume and Issue:
21(1)
Published: Oct. 11, 2022
Oncolytic
viruses
(OVs)
represent
a
new
class
of
multi-modal
immunotherapies
for
cancer,
with
OV-elicited
antitumor
immunity
being
key
to
their
overall
therapeutic
efficacy.
Currently,
the
clinical
effectiveness
OV
as
monotherapy
remains
limited,
and
thus
investigators
have
been
exploring
various
combinations
other
anti-cancer
agents
demonstrated
improved
As
cancer
cells
evolved
alter
signaling
pathways
enhanced
cell
proliferation,
progression
metastasis,
these
cellular
molecular
changes
offer
promising
targets
rational
therapy
design.
In
this
regard,
molecules
in
relevant
or/and
immune
cells,
such
EGFR-KRAS
(e.g.,
KRASG12C),
PI3K-AKT-mTOR,
ERK-MEK,
JAK-STAT,
p53,
PD-1-PD-L1,
epigenetic,
or
histone
deacetylases,
cGAS-STING)
are
currently
under
investigation
potential
synergize
modulate
milieu
tumor
microenvironment
(TME),
thereby
improving
sustaining
immunity.
many
small
molecule
modulators
developed
shown
strong
potential,
here
we
review
findings
related
both
OV-mediated
immunotherapy
utility
immuno-oncology.
Then,
focus
on
discussion
rationales
strategies
combining
selected
targeting
TME
enhance
Finally,
provide
perspectives
viewpoints
application
novel
experimental
systems
technologies
that
can
propel
exciting
branch
medicine
into
bright
future.
Journal of Immunology Research,
Journal Year:
2022,
Volume and Issue:
2022, P. 1 - 9
Published: March 18, 2022
With
the
huge
therapeutic
potential,
cancer
immunotherapy
is
expected
to
become
mainstream
of
treatment.
In
current
field
immunotherapy,
there
are
mainly
five
types.
Immune
checkpoint
blockade
therapy
one
most
promising
directions.
Adoptive
cell
an
important
component
immunotherapy.
The
with
vaccine
capable
prevention.
Cytokine
pillars
Oncolytic
a
novel
which
significantly
lower
incidence
serious
adverse
reactions.
recent
positive
results
many
clinical
trials
may
herald
good
prospects.
But
still
challenges
in
broad
implementation
Such
as
cannot
act
on
all
tumors,
and
it
has
effects
including
but
not
limited
nonspecific
autoimmunity
inflammation.
Here,
we
center
progress
made
within
last
5
years
And
discuss
theoretical
background,
well
opportunities
Future Oncology,
Journal Year:
2022,
Volume and Issue:
18(24), P. 2713 - 2732
Published: July 12, 2022
Despite
advances
in
treatment,
cancer
remains
a
leading
cause
of
death
worldwide.
Although
treatment
strategies
are
continually
progressing,
cancers
have
evolved
many
mechanisms
for
evading
therapies
and
the
host
immune
system.
Oncolytic
viruses
(OVs)
could
provide
much-needed
option
that
resistant
to
existing
treatments.
OVs
can
be
engineered
specifically
target
kill
cells,
while
simultaneously
triggering
an
response
at
site
infection.
This
review
will
focus
on
challenges
developing
successful
OV
translation
clinical
practice,
discussing
innovative
being
used
optimize
potential
OVs.
Here,
we
also
explore
current
landscape
prospects
early
development.
Frontiers in Cellular and Infection Microbiology,
Journal Year:
2023,
Volume and Issue:
13
Published: March 15, 2023
Recent
reports
have
revealed
that
oncolytic
viruses
(OVs)
play
a
significant
role
in
cancer
therapy.
The
infection
of
OVs
such
as
vaccinia
virus
(OVV),
vesicular
stomatitis
(VSV),
parvovirus,
mammalian
reovirus
(MRV),
human
adenovirus,
Newcastle
disease
(NDV),
herpes
simplex
(HSV),
avian
(ARV),
Orf
(ORFV),
inactivated
Sendai
(ISV),
enterovirus,
and
coxsackievirus
offer
unique
opportunities
immunotherapy
through
diverse
dynamic
pathways.
This
mini-review
focuses
on
the
mechanisms
OVs-mediated
virotherapy
their
effects
immunogenic
cell
death
(ICD),
apoptosis,
autophagy
regulation
immune
system.
Viruses,
Journal Year:
2023,
Volume and Issue:
15(8), P. 1645 - 1645
Published: July 28, 2023
Oncolytic
viruses
have
positively
impacted
cancer
immunotherapy
over
the
past
20
years.
Both
natural
and
genetically
modified
shown
promising
results
in
treating
various
cancers.
Various
regulatory
authorities
worldwide
approved
four
commercial
oncolytic
viruses,
more
are
being
developed
to
overcome
this
limitation
obtain
better
anti-tumor
responses
clinical
trials
at
stages.
Faster
advancements
translating
research
into
commercialization
of
a
comprehensive
understanding
modification
strategies
will
widen
current
knowledge
future
technologies
related
development
viruses.
In
review,
we
discuss
virus
engineering
progress
achieve
virotherapeutics.
Cytokine & Growth Factor Reviews,
Journal Year:
2023,
Volume and Issue:
70, P. 1 - 12
Published: Jan. 31, 2023
Oncolytic
viruses
(OVs)
represent
a
highly
promising
treatment
strategy
for
wide
range
of
cancers,
by
mediating
both
the
direct
killing
tumor
cells
as
well
mobilization
antitumor
immune
responses.
As
many
OVs
circulate
in
human
population,
preexisting
OV-specific
responses
are
prevalent.
Indeed,
neutralizing
antibodies
(NAbs)
abundantly
present
population
commonly
used
OVs,
such
Adenovirus
type
5
(Ad5),
Herpes
Simplex
Virus-1
(HSV-1),
Vaccinia
virus,
Measles
and
Reovirus.
This
review
discusses
(pre)clinical
evidence
regarding
effect
immunity
against
on
two
distinct
aspects
OV
therapy;
infection
spread,
response
induced
upon
therapy.
Combined,
this
provides
that
consideration
is
crucial
realizing
full
potential
therapeutic
implementation
OVs.
Future
investigation
current
gaps
knowledge
highlighted
should
yield
more
complete
understanding
topic,
ultimately
allowing
better
personalized
therapies.