Exploring CAR-macrophages in non-tumor diseases: Therapeutic potential beyond cancer
Yizhao Chen,
No information about this author
Qianling Xin,
No information about this author
Mengjuan Zhu
No information about this author
et al.
Journal of Advanced Research,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
After
significant
advancements
in
tumor
treatment,
personalized
cell
therapy
based
on
chimeric
antigen
receptors
(CAR)
holds
promise
for
transforming
the
management
of
various
diseases.
CAR-T
therapy,
first
approved
CAR
product,
has
demonstrated
therapeutic
potential
treating
infectious
diseases,
autoimmune
disorders,
and
fibrosis.
CAR-macrophages
(CAR-Ms)
are
emerging
as
a
promising
approach
immune
particularly
solid
highlighting
feasibility
using
macrophages
to
eliminate
pathogens
abnormal
cells.
Language: Английский
In vivo anti-FAP CAR T therapy reduces fibrosis and restores liver homeostasis in metabolic dysfunction-associated steatohepatitis
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 27, 2025
In
this
study,
we
aimed
to
determine
the
efficacy
of
in
vivo
chimeric
antigen
receptor
(CAR)
T
cell
therapy,
generated
by
targeted
lipid
nanoparticles
(t-LNPs),
as
an
anti-fibrotic
metabolic
dysfunction-associated
steatotic
liver
disease.
Hepatic
fibrosis
is
a
key
predictor
mortality
disease,
driven
fibrogenic
hepatic
stellate
cells
(HSCs).
heart,
targeting
fibroblast
activation
protein
alpha
(FAP)
reduce
murine
cardiac
fibrosis.
However,
value
approach
unknown.
We
explored
potential
vivo-generated
anti-FAP
CAR
steatohepatitis
(MASH),
highly
prevalent
disease
with
no
approved
therapies.
first
established
that
FAP
expression
both
human
and
MASH
specific
HSCs.
then
used
flow
cytometry,
Sirius
Red
morphometry,
digital
pathology
analysis,
single
nuclear
RNA-sequencing
assess
impact
therapy
on
MASH.
Anti-CD5
targeted-LNPs
carrying
anti-FAPCAR
mRNA
generate
activated,
transient
cells,
which
significantly
reduced
depleting
pro-fibrogenic
HSCs,
modulating
immune
endothelial
hepatocytes
non-cell
autonomous
manner
mitigate
inflammation
restore
homeostasis.
These
findings
reinforce
attenuate
morbid
pervasive
through
integrated,
multicellular
salutary
effects.
RNA-based
treatment
transiently
reprograms
target
scar-forming
fatty
thus
improving
health
overall.
Language: Английский
Exploration of the role of immune cells and cell therapy in hepatocellular carcinoma
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: April 16, 2025
Hepatocellular
carcinoma
stands
as
one
of
the
foremost
contributors
to
cancer-associated
fatalities
globally,
and
limitations
traditional
treatment
methods
have
prompted
researchers
explore
new
therapeutic
options.
Recently,
cell
therapy
has
emerged
a
promising
approach
for
HCC,
showing
significant
potential
in
improving
patient
outcomes.
This
review
article
explores
use
covering
different
types,
mechanisms
behind
their
effectiveness,
recent
advancements
clinical
trials,
ongoing
challenges.
aims
provide
insightful
perspectives
future
research
applications
treating
HCC
by
synthesizing
current
knowledge.
Language: Английский
Revisiting the role of cancer-associated fibroblasts in tumor microenvironment
Xiaolei Lan,
No information about this author
Wenyang Li,
No information about this author
Kai Zhao
No information about this author
et al.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: April 17, 2025
Cancer-associated
fibroblasts
(CAFs)
are
integral
components
of
the
tumor
microenvironment
playing
key
roles
in
progression,
metastasis,
and
therapeutic
resistance.
However,
challenges
persist
understanding
their
heterogeneity,
origin,
functional
diversity.
One
major
obstacle
is
lack
standardized
naming
conventions
for
CAF
subpopulations,
with
current
systems
failing
to
capture
full
complexity.
Additionally,
identification
CAFs
hindered
by
absence
specific
biomarkers,
limiting
precision
diagnostic
strategies.
In
vitro
culture
conditions
often
fail
maintain
vivo
characteristics
CAFs,
which
complicates
study
translation
findings
clinical
practice.
Although
detection
methods,
such
as
antibodies,
mRNA
probes,
single-cell
transcriptomics,
offer
insights
into
biology,
they
standardization
provide
reliable
quantitative
measures.
Furthermore,
dynamic
interactions
between
cells,
immune
cells
within
TME
remain
insufficiently
understood,
role
evasion
therapy
resistance
an
area
ongoing
research.
Understanding
how
influence
drug
response
essential
developing
more
effective
cancer
therapies.
This
review
aims
in-depth
analysis
research,
propose
future
research
directions,
emphasize
need
improved
CAF-targeted
By
addressing
these
gaps,
it
seeks
highlight
potential
targets
overcoming
enhancing
efficacy
treatments.
Language: Английский