Strategies to Overcome Antigen Heterogeneity in CAR-T Cell Therapy
Bohan Zhang,
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Jiawen Wu,
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Hua Jiang
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et al.
Cells,
Journal Year:
2025,
Volume and Issue:
14(5), P. 320 - 320
Published: Feb. 20, 2025
Chimeric
antigen
receptor
(CAR)
gene-modified
T-cell
therapy
has
achieved
significant
success
in
the
treatment
of
hematological
malignancies.
However,
this
not
yet
made
breakthroughs
solid
tumors
and
still
faces
issues
resistance
relapse
cancers.
A
major
reason
for
these
problems
is
antigenic
heterogeneity
tumor
tissues.
This
review
outlines
encountered
CAR-T
cell
corresponding
strategies
to
address
it.
These
include
using
combination
increase
abundance
target
antigens,
optimizing
structure
CARs
enhance
sensitivity
low-density
developing
multi-targeted
cells,
reprogramming
TME
activate
endogenous
immunity.
approaches
offer
new
directions
overcoming
therapy.
Language: Английский
The current socioeconomic and regulatory landscape of immune effector cell therapies
Frontiers in Medicine,
Journal Year:
2024,
Volume and Issue:
11
Published: Dec. 4, 2024
Immune
cell
effector
therapies,
including
chimeric
antigen
receptor
(CAR)-T
cells,
T-cell
(TCR)
T
natural
killer
(NK)
and
macrophage-based
represent
a
transformative
approach
to
cancer
treatment,
harnessing
the
immune
system
target
eradicate
malignant
cells.
CAR-T
therapy,
most
established
among
these,
involves
engineering
cells
express
CARs
specific
antigens,
showing
remarkable
efficacy
in
hematologic
malignancies
like
leukemias,
B-cell
lymphomas,
multiple
myeloma.
Similarly,
TCR-modified
which
reprogram
recognize
intracellular
tumor
antigens
presented
by
major
histocompatibility
complex
(MHC)
molecules,
offer
promise
for
range
of
solid
tumors.
NK-cell
therapies
leverage
NK
cells'
innate
cytotoxicity,
providing
an
allogeneic
that
avoids
some
immune-related
complications
associated
with
T-cell-based
therapies.
Macrophage-based
still
early
stages
development,
focus
on
reprogramming
macrophages
stimulate
response
against
microenvironment.
Despite
their
promise,
socioeconomic
regulatory
challenges
hinder
accessibility
scalability
These
treatments
are
costly,
currently
exceeding
$400,000
per
patient,
creating
significant
disparities
access
based
status
geographic
location.
The
high
manufacturing
costs
stem
from
personalized,
labor-intensive
processes
harvesting,
modifying,
expanding
patients'
Moreover,
logistics
delivering
these
limit
reach,
particularly
low-resource
settings.
Regulatory
pathways
further
complicate
landscape.
In
United
States.,
Food
Drug
Administrations'
(FDA)
accelerated
approval
cell-based
facilitate
innovation
but
do
not
address
cost-related
barriers.
Europe,
European
Medicines
Agency
(EMA)
offers
adaptive
pathways,
yet
decentralized
reimbursement
systems
create
uneven
across
member
states.
Additionally,
differing
standards
quality
control
worldwide
pose
hurdles
global
harmonization
access.
To
expand
reach
multipronged
is
needed-streamlined
frameworks,
policies
reduce
treatment
costs,
international
collaborations
standardize
manufacturing.
Addressing
obstacles
essential
make
life-saving
accessible
broader
patient
population
worldwide.
We
present
literature
review
current
landscape
barriers
approved
standard
care
therapy
at
various
levels.
Language: Английский
Exploring neuroblastoma’s cellular microenvironment: A novel approach using cellular automata to model Celyvir treatment
Computers in Biology and Medicine,
Journal Year:
2025,
Volume and Issue:
188, P. 109782 - 109782
Published: Feb. 12, 2025
Language: Английский
Principles of Immunotherapy and Novel Immunotherapeutic Agents for Pediatric Cancer Management
Published: Jan. 1, 2025
Language: Английский
Biomarker-Driven Approaches to Bone Metastases: From Molecular Mechanisms to Clinical Applications
Youssef Elshimy,
No information about this author
Ala’a Aldeen Alkhatib,
No information about this author
Bilal Atassi
No information about this author
et al.
Biomedicines,
Journal Year:
2025,
Volume and Issue:
13(5), P. 1160 - 1160
Published: May 10, 2025
Bone
metastases
represent
a
critical
complication
in
oncology,
frequently
indicating
advanced
malignancy
and
substantially
reducing
patient
quality
of
life.
This
review
provides
comprehensive
analysis
the
complex
interactions
between
tumor
cells
bone
microenvironment,
emphasizing
relevance
"seed
soil"
hypothesis,
RANK/RANKL/OPG
signaling
axis,
Wnt
pathways
that
collectively
drive
metastatic
progression.
The
molecular
cellular
mechanisms
underlying
formation
osteolytic
osteoblastic
lesions
are
examined
detail,
with
particular
focus
on
their
implications
for
associated
breast,
prostate,
lung,
other
cancers.
A
central
component
this
is
categorization
pathological
biomarkers
into
four
types:
diagnostic,
prognostic,
predictive,
monitoring.
We
provide
evaluation
circulating
(CTCs),
turnover
markers
(such
as
TRACP-5b
CTX),
imaging
(including
PET/CT
MRI),
novel
genomic
signatures.
These
offer
valuable
insights
early
detection,
enhanced
risk
stratification,
optimized
therapeutic
decision-making.
Furthermore,
emerging
strategies
immunotherapy
bone-targeted
treatments
discussed,
highlighting
potential
biomarker-guided
precision
medicine
to
enhance
personalized
care.
distinctiveness
lies
its
integrative
approach,
combining
fundamental
pathophysiological
latest
developments
biomarker
discovery
innovation.
By
synthesizing
evidence
across
various
cancer
types
categories,
we
cohesive
framework
aimed
at
advancing
both
scientific
understanding
clinical
management
metastases.
Language: Английский
An Optimized Liquid Chromatography–Mass Spectrometry Method for Ganglioside Analysis in Cell Lines
Cells,
Journal Year:
2024,
Volume and Issue:
13(19), P. 1640 - 1640
Published: Oct. 2, 2024
Gangliosides
are
glycosphingolipids
composed
of
a
sialylated
glycan
head
group
and
ceramide
backbone.
These
anionic
lipids
form
lipid
rafts
play
crucial
roles
in
regulating
various
proteins
involved
signal
transduction,
adhesion,
cell-cell
recognition.
Neuroblastoma,
pediatric
cancer
the
sympathetic
nervous
system,
is
treated
with
intensive
chemotherapy,
radiation,
an
antibody
targeting
GD2
ganglioside.
critical
neuroblastoma
development
serve
as
therapeutic
targets,
making
it
essential
to
establish
reliable,
rapid,
cost-effective
method
for
profiling
gangliosides,
particularly
one
capable
isomeric
separation
intact
species.
In
this
study,
liquid
chromatography-mass
spectrometry
(LC-MS)
was
optimized
using
standard
followed
by
optimization
sphingolipid
extraction
methods
from
cell
lines
comparing
Folch
absolute
methanol
techniques.
Percent
recovery
number
identified
sphingolipids
were
used
evaluate
analytical
merits
these
methods.
A
gangliosides
calibration
curve
demonstrated
excellent
linearity
(R
Language: Английский