Recent developments in myeloid immune modulation in cancer therapy
Trends in cancer,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
Language: Английский
Adoptive T Cell Therapy Targeting MAGE-A4
Kapil Chandora,
No information about this author
Akshay Chandora,
No information about this author
Anwaar Saeed
No information about this author
et al.
Cancers,
Journal Year:
2025,
Volume and Issue:
17(3), P. 413 - 413
Published: Jan. 26, 2025
MAGE
A4
(Melanoma
Antigen
Gene
A4)
is
a
cancer
testis
antigen
(CTA)
that
expressed
normally
in
germline
cells
(testis/embryonic
tissues)
but
absent
somatic
cells.
The
CTA
variety
of
tumor
types,
like
synovial
sarcoma,
ovarian
and
non-small
cell
lung
cancer.
Having
its
expression
profile
limited
to
has
made
sought-after
immunotherapeutic
target
certain
malignancies.
In
this
review,
we
focus
on
MAGE-A4’s
function
expression,
current
clinical
trials
involving
targeted
immunotherapy
approaches,
challenges
opportunities
facing
therapeutics.
Language: Английский
Gold Nanoparticles Synthesized with Triple-Negative Breast Cancer Cell Lysate Enhance Antitumoral Immunity: A Novel Synthesis Method
Pharmaceuticals,
Journal Year:
2025,
Volume and Issue:
18(3), P. 330 - 330
Published: Feb. 26, 2025
Background:
Gold
nanoparticles
enhance
immunity,
promotes
antigen
uptake
by
antigen-presenting
cells
(APCs),
and
boost
the
response
against
tumor
antigens;
therefore,
they
are
a
promising
delivery
vehicle.
Tumor
lysates
have
shown
favorable
responses
as
inductors
of
anti-cancer
but
effectiveness
these
treatments
could
be
improved.
Hybrid
nanosystems
gold
with
biomolecules
been
show
alternative
on
uptake,
activation
immune
system.
Objectives:
This
study’s
objective
was
to
develop
method
synthesizing
employing
triple-negative
breast
cancer
(4T1)
cell
lysate
(AuLtNps)
reducing
agent
increase
immunogenicity
cells.
Methods:
Nanoparticle
formation,
size,
ζ
potential
were
confirmed
surface
plasmon
resonance,
dynamic
light
scattering,
transmission
electron
microscopy.
Protein
concentration
quantified
using
Pierce
BCA
assay.
The
cytotoxic
effects
murine
macrophages
assessed,
along
nanoparticle
via
epifluorescence
Using
model,
cytokine
secretion
profiles
determined,
efficacy
in
inhibiting
implantation
4T1
model
evaluated.
Results/Conclusions:
AuLtNps
exhibited
higher
protein
content
than
alone,
leading
increased
phagocytosis
macrophages,
Cytokine
analysis
showed
proinflammatory
response,
CD8+
CD22+
lymphocytes
upregulation
APC
markers
(CD14,
CD80,
CD86,
MHC
II+).
Splenocytes
demonstrated
specific
lysis
up
40%
In
AuLtNPs
effectively
inhibited
implantation,
achieving
an
improved
90-days
survival
rate,
highlighting
their
immunotherapy
for
cancer.
Language: Английский
Melanoma-associated fibroblasts in tumor-promotion flammation and antitumor immunity: novel mechanisms and potential immunotherapeutic strategies
Qiujun Zhou,
No information about this author
Xiaoliang Jin,
No information about this author
Ying Zhao
No information about this author
et al.
Human Molecular Genetics,
Journal Year:
2024,
Volume and Issue:
33(13), P. 1186 - 1193
Published: March 27, 2024
Abstract
Melanoma,
renowned
for
its
aggressive
behavior
and
resistance
to
conventional
treatments,
stands
as
a
formidable
challenge
in
the
oncology
landscape.
The
dynamic
complex
interplay
between
cancer
cells
tumor
microenvironment
has
gained
significant
attention,
revealing
Melanoma-Associated
Fibroblasts
(MAFs)
central
players
disease
progression.
heterogeneity
of
MAFs
endows
them
with
dual
role
melanoma.
This
exhaustive
review
seeks
not
only
shed
light
on
multifaceted
roles
orchestrating
tumor-promoting
inflammation
but
also
explore
their
involvement
antitumor
immunity.
By
unraveling
novel
mechanisms
underlying
MAF
functions,
this
aims
provide
comprehensive
understanding
impact
melanoma
development.
Additionally,
it
delves
into
potential
leveraging
innovative
immunotherapeutic
strategies,
offering
new
avenues
enhancing
treatment
outcomes
challenging
realm
therapeutics.
Language: Английский
Exploring structure-directed immunogenic cytotoxicity of arginine-rich peptides for cytolysis-induced immunotherapy of cancer
Liu Huang,
No information about this author
Ang Li,
No information about this author
Han-jie Liu
No information about this author
et al.
Bioorganic & Medicinal Chemistry,
Journal Year:
2024,
Volume and Issue:
116, P. 117984 - 117984
Published: Nov. 8, 2024
Language: Английский
Engineered immune cell-based therapeutics for female reproductive tract cancers: Advances and future prospects
Nazim Nazeer,
No information about this author
Rimpa Manna,
No information about this author
S.K. Shukla
No information about this author
et al.
Journal of Reproductive Healthcare and Medicine,
Journal Year:
2024,
Volume and Issue:
5, P. 14 - 14
Published: Nov. 28, 2024
Cancers
of
the
reproductive
tract
are
one
major
causes
deaths
in
women.
The
higher
rate
mortality
among
these
cancers
mainly
due
to
late
stage
disease
detection
and
resistance
existing
drugs.
As
research
progresses,
personalized
medicine,
which
involves
tailoring
treatments
unique
characteristics
each
patient’s
tumor,
is
expected
play
a
significant
role
future.
Engineered
immune
cells
such
as
engineered
dendritic
cells,
chimeric
antigen
receptor
(CAR)
T-cells,
natural
killer
(NK)
have
emerged
an
innovative
approach
cure
female
(FRCs).
These
designed
boost
system’s
ability
identify
remove
cancer
offering
new
therapeutic
opportunities
for
patients
with
limited
treatment
options.
present
review
highlights
applicability
various
cell-based
approaches
treat
FRCs.
It
also
outlines
potential
combining
nanoparticle-based
engineering
strategies
further
enhance
effectiveness
cell
through
improving
delivery
modulators.
Overall,
article
promising
improve
outcomes
Language: Английский
Immunoengineering a Future of Molecular, Material, and Cellular Therapeutics
The Journal of Immunology,
Journal Year:
2024,
Volume and Issue:
212(2), P. 167 - 168
Published: Jan. 2, 2024
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Manager
Jeffrey
A.
Hubbell;
Immunoengineering
a
Future
of
Molecular,
Material,
and
Cellular
Therapeutics.
J
Immunol
15
January
2024;
212
(2):
167–168.
https://doi.org/10.4049/jimmunol.2300773
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