Next-Generation Therapeutic Antibodies for Cancer Treatment: Advancements, Applications, and Challenges
A. Raja,
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Abhishek Kasana,
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Vaishali Verma
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et al.
Molecular Biotechnology,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Sept. 2, 2024
Language: Английский
Leptomeningeal metastasis and cancer immunotherapy
Rob Smeyers,
No information about this author
Alia Fazal-Salom,
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Ján Remšík
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et al.
Elsevier eBooks,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
Language: Английский
Immune Cell Interplay in the Fight Against GBM
Nico Vallieri,
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Angeliki Datsi
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Cancers,
Journal Year:
2025,
Volume and Issue:
17(5), P. 817 - 817
Published: Feb. 26, 2025
Despite
multimodal
therapies,
the
treatment
of
glioblastoma
remains
challenging.
In
addition
to
very
complex
mechanisms
cancer
cells,
including
specialized
phenotypes
that
enable
them
proliferate,
invade
tissues,
and
evade
immunosurveillance,
they
exhibit
a
pronounced
resistance
chemo-
radiotherapy.
More
advanced
tumors
create
hypoxic
environment
supports
their
proliferation
survival,
while
robust
angiogenesis
ensures
constant
supply
nutrients.
GBM,
these
structures
are
contribute
creation
maintenance
highly
immunosuppressive
microenvironment
promotes
tumor
growth
immune
escape.
addition,
high
accumulation
tumor-infiltrating
leukocytes
other
expression
checkpoint
molecules,
low
mutational
burden,
i.e.,
number
neoantigens,
hallmarks
GBM
challenge
therapeutic
approaches.
Here,
we
review
exploits
support
potential
treatments.
These
include
new
chemotherapeutics,
treating
fields,
small
compounds
targeting
or
blockers
tyrosine
kinases
inhibit
cell
survival.
focus
on
immunotherapies
such
as
blockade
in
particular
vaccination
with
dendritic
cells
CAR-T
which
can
either
kill
directly
bypass
immunosuppression
by
modulating
boosting
patient's
own
response.
Language: Английский
T cells in the microenvironment of solid pediatric tumors: the case of neuroblastoma
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: Feb. 28, 2025
Neuroblastoma
(NB)
is
an
immunologically
“cold”
tumor
with
poor
or
no
inflamed
substrates
as
most
of
solid
pediatric
tumors
(SPT).
Consistent
data
indicate
that
NB
microenvironment
(TME)
dominated
by
myeloid
cells,
little
(but
variable)
T
cell
infiltration.
The
obstacles
to
lymphocyte
infiltration
and
their
anti-tumor
activity
are
due
different
immune
evasion
strategies,
including
loss
HLA
Class
I
molecules,
high
expression
checkpoint
molecular
ligands
leading
exhaustion
effector
(and
NK)
induction
regulatory,
stromal
cells
secretion
immunosuppressive
mediators.
In
odds
adult
tumors,
displays
weak
immunogenicity
caused
intrinsic
low
mutational
burden
scant
neoepitopes
in
the
context
MHC-class
antigens
which,
turn,
particularly
poorly
expressed
on
thus
inducing
responses.
addition,
generated
from
embryonal
result
transcriptional
abnormalities
not
accumulation
genetic
mutations
over
time,
further
explaining
immunogenicity.
immunogenic
molecules
associated
production
factors
which
downregulate
activity,
limited
efficacy
new
drugs
NB,
inhibitors.
This
review
focused
examining
role
regulatory
infiltrating
TME
taking
into
account
repertoire,
phenotype,
function,
plasticity
and,
importantly,
predictive
value
for
defining
novel
targets
therapy.
Language: Английский
Mechanistic insights into resistance mechanisms to T cell engagers
Liping Cao,
No information about this author
Gabrielle Leclercq-Cohen,
No information about this author
Christian Klein
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et al.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: April 22, 2025
T
cell
engagers
(TCEs)
represent
a
groundbreaking
advancement
in
the
treatment
of
B
and
plasma
malignancies
are
emerging
as
promising
therapeutic
approach
for
solid
tumors.
These
molecules
harness
cells
to
bind
eliminate
cancer
cells,
effectively
bypassing
need
antigen-specific
recognition.
Despite
their
established
clinical
efficacy,
subset
patients
is
either
refractory
TCE
(e.g.
primary
resistance)
or
develops
resistance
during
course
therapy
acquired
treatment-induced
resistance).
In
this
review
we
comprehensively
describe
mechanisms
TCEs,
occurring
both
preclinical
models
trials
with
particular
emphasis
on
cellular
molecular
pathways
underlying
process.
We
classify
these
into
tumor
intrinsic
extrinsic
ones.
Tumor
encompass
changes
within
that
impact
cell-mediated
cytotoxicity,
including
antigen
loss,
expression
immune
checkpoint
inhibitory
ligands
intracellular
render
resistant
killing.
involve
factors
external
presence
an
immunosuppressive
microenvironment
(TME)
reduced
functionality.
further
propose
actionable
strategies
overcome
offering
potential
avenues
enhancing
efficacy
clinic.
Language: Английский
Regulatory T Cells in Tumor Microenvironment: Therapeutic Approaches and Clinical Implications
Cell Biology International,
Journal Year:
2025,
Volume and Issue:
unknown
Published: May 14, 2025
ABSTRACT
Regulatory
T
cells
(Tregs),
previously
referred
to
as
suppressor
cells,
represent
a
distinct
subset
of
CD4+
that
are
uniquely
specialized
for
immune
suppression.
They
characterized
by
the
constitutive
expression
transcription
factor
FoxP3
in
their
nuclei,
along
with
CD25
(the
IL‐2
receptor
α‐chain)
and
CTLA‐4
on
cell
surface.
Tregs
not
only
restrict
natural
killer
cell‐mediated
cytotoxicity
but
also
inhibit
proliferation
CD8+
T‐cells
suppress
interferon‐γ
secretion
ultimately
impairing
an
effective
antitumor
response.
Treg
widely
recognized
significant
barrier
effectiveness
tumor
immunotherapy
clinical
settings.
Extensive
research
has
consistently
shown
play
pivotal
role
facilitating
initiation
progression.
Conversely,
depletion
been
linked
marked
delay
growth
development.
Language: Английский
Tumor Immune Microenvironment in Intrahepatic Cholangiocarcinoma: Regulatory Mechanisms, Functions, and Therapeutic Implications
Cancers,
Journal Year:
2024,
Volume and Issue:
16(20), P. 3542 - 3542
Published: Oct. 20, 2024
Treatment
options
for
intrahepatic
cholangiocarcinoma
(iCCA),
a
highly
malignant
tumor
with
poor
prognosis,
are
limited.
Recent
developments
in
immunotherapy
and
immune
checkpoint
inhibitors
(ICIs)
have
offered
new
hope
treating
iCCA.
However,
several
issues
remain,
including
the
identification
of
reliable
biomarkers
response
to
ICIs
immune-based
combinations.
Tumor
microenvironment
(TIME)
these
hepatobiliary
tumors
has
been
evaluated
is
under
assessment
this
setting
order
boost
efficacy
convert
immunologically
"cold"
"hot"
tumors.
Herein,
review
TIME
ICCA
its
critical
function
immunotherapy.
Moreover,
paper
also
discusses
potential
avenues
future
research,
novel
targets
emerging
treatment
plans
aimed
increase
effectiveness
survival
rates
iCCA
patients.
Language: Английский
Bispecific T-Cell Engagers (BiTEs) in Immunotherapy
Advances in medical diagnosis, treatment, and care (AMDTC) book series,
Journal Year:
2024,
Volume and Issue:
unknown, P. 205 - 234
Published: Aug. 28, 2024
Bispecific
T-cell
engagers
(BiTEs)
is
a
novel
subclass
of
T-cell-engaging
bispecific
antibodies
(bulbs)
that
are
promising
for
the
treatment
cancer.
BiTEs
direct
cytotoxic
activity
towards
malignant
cells,
resulting
in
targeted
destruction
tumor
cells.
This
chapter
provides
an
overview
current
landscape
BiTE
therapy,
highlighting
its
efficacy
hematologic
malignancies
such
as
B-cell
acute
lymphoblastic
leukemia
(B-ALL)
and
exploring
potential
applications
solid
tumors.
Additionally,
challenges
immunogenicity,
stability,
off-target
effects
were
discussed,
alongside
ongoing
efforts
to
overcome
these
obstacles
through
protein
engineering
combination
therapies.
Future
directions
therapy
include
optimizing
delivery
methods
strategies.
Overall,
represents
approach
cancer
treatment,
with
revolutionize
immunotherapy
improve
patient
outcomes.
Language: Английский
Infections during novel myeloma therapies
Leukemia & lymphoma/Leukemia and lymphoma,
Journal Year:
2024,
Volume and Issue:
unknown, P. 1 - 13
Published: Nov. 18, 2024
New
generation
therapies
such
as
bispecific
antibodies
(BsAb),
chimeric
antigen
receptor
T-cell
therapy
(CAR
T)
and
antibody-drug
conjugates
(ADC)
have
revolutionized
the
treatment
of
relapsed/refractory
multiple
myeloma
(RRMM).
However,
there
is
emerging
evidence
increased
infection
risk
associated
with
these
treatments
in
clinical
trials
observational
settings.
This
may
be
mediated
by
on-target,
off-tumor
side
effects
cytokine
release
syndrome,
hypogammaglobulinaemia
cytopenias,
disease-related
humoral
impairment
consequences
previous
lines
treatment.
While
bacterial
viral
pathogens
predominate,
reactivation
latent
opportunistic
infections
also
warrant
attention.
review
characterizes
epidemiology
novel
for
RRMM
to
guide
prophylaxis
antimicrobial
prescribing
this
patient
population
highlights
future
areas
focus
inform
ongoing
prevention
strategies.
Language: Английский