International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(14), P. 7960 - 7960
Published: July 21, 2024
Gamma
delta
(γδ)
T
cells
are
a
heterogeneous
population
of
that
play
roles
in
inflammation,
host
tissue
repair,
clearance
viral
and
bacterial
pathogens,
regulation
immune
processes,
tumor
surveillance.
Recent
research
suggests
these
the
main
skin
produce
interleukin-17
(I-17).
Furthermore,
γδ
exhibit
memory-cell-like
characteristics
mediate
repeated
episodes
psoriatic
inflammation.
found
epithelial
tissues,
where
many
cancers
develop.
There,
they
participate
antitumor
immunity
as
cytotoxic
or
coordinators.
also
defense,
surveillance,
homeostasis.
The
aim
this
review
is
to
present
importance
physiological
pathological
diseases,
such
psoriasis,
atopic
dermatitis,
autoimmune
cancer,
lymphoma.
Signal Transduction and Targeted Therapy,
Journal Year:
2023,
Volume and Issue:
8(1)
Published: Nov. 22, 2023
The
intricacy
of
diseases,
shaped
by
intrinsic
processes
like
immune
system
exhaustion
and
hyperactivation,
highlights
the
potential
renormalization
as
a
promising
strategy
in
disease
treatment.
In
recent
years,
our
primary
focus
has
centered
on
γδ
T
cell-based
immunotherapy,
particularly
pioneering
use
allogeneic
Vδ2
Molecular Cancer,
Journal Year:
2023,
Volume and Issue:
22(1)
Published: Feb. 15, 2023
Abstract
As
a
nontraditional
T-cell
subgroup,
γδT
cells
have
gained
popularity
in
the
field
of
immunotherapy
recent
years.
They
extraordinary
antitumor
potential
and
prospects
for
clinical
application.
Immune
checkpoint
inhibitors
(ICIs),
which
are
efficacious
tumor
patients,
become
pioneer
drugs
since
they
were
incorporated
into
practice.
In
addition,
that
infiltrated
tissues
found
to
be
state
exhaustion
or
anergy,
there
is
upregulation
many
immune
checkpoints
(ICs)
on
their
surface,
suggesting
similar
ability
respond
ICIs
as
traditional
effector
T
cells.
Studies
shown
targeting
ICs
can
reverse
dysfunctional
microenvironment
(TME)
exert
effects
by
improving
γδT-cell
proliferation
activation
enhancing
cytotoxicity.
Clarification
functional
TME
mechanisms
underlying
interaction
with
will
solidify
combined
good
treatment
option.
Cells,
Journal Year:
2024,
Volume and Issue:
13(2), P. 146 - 146
Published: Jan. 12, 2024
This
last
decade,
chimeric
antigen
receptor
(CAR)
T-cell
therapy
has
become
a
real
treatment
option
for
patients
with
B-cell
malignancies,
while
multiple
efforts
are
being
made
to
extend
this
other
malignancies
and
broader
patient
populations.
However,
several
limitations
remain,
including
those
associated
the
time-consuming
highly
personalized
manufacturing
of
autologous
CAR-Ts.
Technologies
establish
"off-the-shelf"
allogeneic
CAR-Ts
low
alloreactivity
currently
developed,
strong
focus
on
gene-editing
technologies.
Although
these
technologies
have
many
advantages,
they
also
limitations,
double-strand
breaks
in
DNA
safety
risks
as
well
lack
modulation.
As
an
alternative,
non-gene-editing
provide
interesting
approach
support
development
future,
possibilities
fine-tuning
gene
expression
easy
development.
Here,
we
will
review
different
ways
can
be
manufactured
discuss
which
used.
The
biggest
hurdles
successful
summarized,
finally,
overview
current
clinical
evidence
comparison
its
counterpart
given.
MedComm,
Journal Year:
2024,
Volume and Issue:
5(10)
Published: Sept. 15, 2024
The
innate
immune
system
serves
as
the
body's
first
line
of
defense,
utilizing
pattern
recognition
receptors
like
Toll-like
to
detect
pathogens
and
initiate
rapid
response
mechanisms.
Following
this
initial
response,
adaptive
immunity
provides
highly
specific
sustained
killing
via
B
cells,
T
antibodies.
Traditionally,
it
has
been
assumed
that
activates
immunity;
however,
recent
studies
have
revealed
more
complex
interactions.
This
review
a
detailed
dissection
composition
function
systems,
emphasizing
their
synergistic
roles
in
physiological
pathological
contexts,
providing
new
insights
into
link
between
these
two
forms
immunity.
Precise
regulation
both
systems
at
same
time
is
beneficial
fight
against
immune-related
diseases,
for
example,
cGAS-STING
pathway
found
play
an
important
role
infections
cancers.
In
addition,
paper
summarizes
challenges
future
directions
field
immunity,
including
latest
single-cell
sequencing
technologies,
CAR-T
cell
therapy,
checkpoint
inhibitors.
By
summarizing
developments,
aims
enhance
our
understanding
complexity
interactions
perspectives
system.
Frontiers in Immunology,
Journal Year:
2023,
Volume and Issue:
14
Published: March 31, 2023
Owing
to
their
antitumor
and
major
histocompatibility
complex
(MHC)-independent
capacities,
γδ
T
cells
have
gained
popularity
in
adoptive
T-cell
immunotherapy
recent
years.
However,
many
unknowns
still
exist
regarding
cells,
few
clinical
data
been
collected.
Therefore,
this
review
aims
describe
all
the
main
features
of
applications
provide
a
systematic
view
current
immunotherapy.
Specifically,
will
focus
on
how
performed
treating
cancers
clinics,
trials
that
conducted
date,
role
pharmaceutical
industry.
Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: March 21, 2024
Comprising
only
1-10%
of
the
circulating
T
cell
population,
γδT
cells
play
a
pivotal
role
in
cancer
immunotherapy
due
to
their
unique
amalgamation
innate
and
adaptive
immune
features.
These
can
secrete
cytokines,
including
interferon-γ
(IFN-γ)
tumor
necrosis
factor-α
(TNF-α),
directly
eliminate
through
mechanisms
like
Fas/FasL
antibody-dependent
cell-mediated
cytotoxicity
(ADCC).
Unlike
conventional
αβT
cells,
target
wide
variety
independently
major
histocompatibility
complex
(MHC)
presentation
function
as
antigen-presenting
(APCs).
Their
ability
recognizing
antigens
non-MHC
restricted
manner
makes
them
an
ideal
candidate
for
allogeneic
immunotherapy.
Additionally,
exhibit
specific
tissue
tropism,
rapid
responsiveness
upon
reaching
cellular
targets,
indicating
high
level
precision
adaptability.
Despite
these
capabilities,
therapeutic
potential
has
been
hindered
by
some
limitations,
abundance,
unsatisfactory
expansion,
limited
persistence,
biology
plasticity.
To
address
issues,
gene-engineering
strategies
use
chimeric
antigen
receptor
(CAR)
therapy,
(TCR)
gene
transfer,
combination
with
engagers
are
being
explored.
This
review
will
outline
progress
various
engineering
strategies,
discuss
implications
challenges
that
lie
ahead,
future
directions
engineered
both
monotherapy
ACS Nano,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 25, 2025
Melanoma
is
the
most
aggressive
type
of
skin
cancers.
Traditional
chemotherapy
and
radiotherapy
have
limited
effectiveness
can
lead
to
systemic
side
effects.
Photodynamic
therapy
(PDT)
a
photoresponsive
cancer
based
on
photosensitizers
generate
reactive
oxygen
species
(ROS)
eradicate
tumor
cells.
Our
previous
study
showed
that
exosomes
derived
from
human
γδ-T
cells
(γδ-T
exosomes)
could
control
Epstein–Barr
virus-associated
tumors.
Here,
we
combined
PDT
for
targeted
photoimmunotherapy
by
membrane
fusion
Chlorin
e6
(Ce6)-loaded
liposomes.
The
functional
surface
proteins,
such
as
CCR5
PD-1,
hybrid
mediated
specific
binding
toward
melanoma
tissues.
cytolytic
molecules,
granzyme
A,
B,
perforin,
granulysin
exosomes,
induced
apoptosis
without
harming
normal
In
response
light
irradiation,
ROS
generation
inside
synergized
with
molecules
induce
promote
immunogenic
cell
death
(ICD).
subsequently
released
damage-associated
molecular
patterns
(DAMPs)
stimulate
dendritic
maturation
antigen-specific
CD4+
CD8+
T-cell
responses,
thereby
enhancing
antitumor
immunity.
This
provides
promising
strategy
combining
photoimmunotherapy,
expanding
clinical
applications
exosome
patients.