Nature Communications,
Год журнала:
2024,
Номер
15(1)
Опубликована: Фев. 6, 2024
Abstract
Antigen-specific
regulatory
T
cells
(Tregs)
suppress
pathogenic
autoreactivity
and
are
potential
therapeutic
candidates
for
autoimmune
diseases
such
as
systemic
lupus
erythematosus
(SLE).
Lupus
nephritis
is
associated
with
to
the
Smith
(Sm)
autoantigen
human
leucocyte
antigen
(HLA)-DR15
haplotype;
hence,
we
investigated
of
Sm-specific
Tregs
(Sm-Tregs)
disease.
Here
identify
a
HLA-DR15
restricted
immunodominant
Sm
cell
epitope
using
biophysical
affinity
binding
assays,
then
high-affinity
receptors
(TCRs)
high-throughput
single-cell
sequencing.
Using
lentiviral
vectors,
transduce
our
lead
TCR
into
derived
from
patients
SLE
who
anti-Sm
positive.
Compared
polyclonal
mock-transduced
Tregs,
Sm-Tregs
potently
pro-inflammatory
responses
in
vitro
disease
progression
humanized
mouse
model
nephritis.
These
results
show
that
promising
therapy
SLE.
Annual Review of Immunology,
Год журнала:
2020,
Номер
38(1), С. 541 - 566
Опубликована: Фев. 4, 2020
Naturally
occurring
CD4+
regulatory
T
cells
(Tregs),
which
specifically
express
the
transcription
factor
FoxP3
in
nucleus
and
CD25
CTLA-4
on
cell
surface,
are
a
functionally
distinct
subpopulation
actively
engaged
maintenance
of
immunological
self-tolerance
homeostasis.
Recent
studies
have
facilitated
our
understanding
cellular
molecular
basis
their
generation,
function,
phenotypic
functional
stability,
adaptability.
It
is
under
investigation
humans
how
or
numerical
Treg
anomalies,
whether
genetically
determined
environmentally
induced,
contribute
to
diseases
such
as
autoimmune
diseases.
Also
being
addressed
Tregs
can
be
targeted
control
physiological
pathological
immune
responses,
for
example,
by
depleting
them
enhance
tumor
immunity
expanding
treat
This
review
discusses
current
immunobiology
normal
disease
states,
with
perspective
realization
Treg-targeting
therapies
clinic.
Abstract
Regulatory
T
cells
(Tregs)
characterized
by
the
expression
of
master
transcription
factor
forkhead
box
protein
p3
(Foxp3)
suppress
anticancer
immunity,
thereby
hindering
protective
immunosurveillance
tumours
and
hampering
effective
antitumour
immune
responses
in
tumour-bearing
hosts,
constitute
a
current
research
hotspot
field.
However,
Tregs
are
also
essential
for
maintenance
tolerance
body
share
many
molecular
signalling
pathways
with
conventional
cells,
including
cytotoxic
primary
mediators
tumour
immunity.
Hence,
inability
to
specifically
target
neutralize
microenvironment
without
globally
compromising
self-tolerance
poses
significant
challenge.
Here,
we
review
recent
advances
characterizing
tumour-infiltrating
focus
on
functional
roles
costimulatory
inhibitory
receptors
Tregs,
evaluate
their
potential
as
clinical
targets,
systematically
summarize
treatment
strategies.
Also,
propose
modalities
integrate
our
increasing
knowledge
phenotype
function
rational
design
checkpoint
inhibitor-based
combination
therapies.
Finally,
possible
strategies
that
can
be
used
develop
Treg-targeted
Frontiers in Immunology,
Год журнала:
2019,
Номер
10
Опубликована: Янв. 31, 2019
Regulatory
T
cells
(Tregs)
are
important
for
the
induction
and
maintenance
of
peripheral
tolerance
therefore,
they
key
in
preventing
excessive
immune
responses
autoimmunity.
In
last
decades,
several
reports
have
been
focussed
on
understanding
biology
Tregs
their
mechanisms
action.
Preclinical
studies
demonstrated
ability
to
delay/prevent
graft
rejection
control
autoimmune
following
adoptive
transfer
vivo.
Due
these
promising
results,
extensively
studied
as
a
potential
new
tool
prevention
and/or
treatment
diseases.
Currently,
solid
organ
transplantation
remains
choice
end-stage
failure.
However,
chronic
ensuing
side
effects
immunosuppressants
represent
main
limiting
factors
acceptance
patient
survival.
Autoimmune
disorders
diseases
caused
by
breakdown
against
self-antigens.
This
is
triggered
either
numerical
or
functional
Treg
defect,
resistance
effector
suppression.
this
scenario,
patients
receiving
high
doses
immunosuppressant
left
susceptible
life-threatening
opportunistic
infections
increased
risk
malignancies.
10
years,
few
phase
I
clinical
trials
aiming
investigate
safety
feasibility
Treg-based
therapy
completed
published,
whilst
an
increasing
numbers
still
ongoing.
The
first
results
showed
II
already
enrolling.
review,
we
describe
our
focussing
primarily
ontogenesis,
action
methods
used
clinic
isolation
expansion.
Furthermore,
will
ongoing
from
with
setting
disorders.
Finally,
discuss
strategies
further
improve
success
therapy.
Signal Transduction and Targeted Therapy,
Год журнала:
2023,
Номер
8(1)
Опубликована: Июнь 19, 2023
T
cells
are
crucial
for
immune
functions
to
maintain
health
and
prevent
disease.
cell
development
occurs
in
a
stepwise
process
the
thymus
mainly
generates
CD4
Signal Transduction and Targeted Therapy,
Год журнала:
2024,
Номер
9(1)
Опубликована: Фев. 5, 2024
Abstract
Extracellular
vesicles
(EVs)
are
nano-sized,
membranous
structures
secreted
into
the
extracellular
space.
They
exhibit
diverse
sizes,
contents,
and
surface
markers
ubiquitously
released
from
cells
under
normal
pathological
conditions.
Human
serum
is
a
rich
source
of
these
EVs,
though
their
isolation
proteins
non-EV
lipid
particles
poses
challenges.
These
transport
various
cellular
components
such
as
proteins,
mRNAs,
miRNAs,
DNA,
lipids
across
distances,
influencing
numerous
physiological
events,
including
those
within
tumor
microenvironment
(TME).
Their
pivotal
roles
in
communication
make
EVs
promising
candidates
for
therapeutic
agents,
drug
delivery
systems,
disease
biomarkers.
Especially
cancer
diagnostics,
EV
detection
can
pave
way
early
identification
offers
potential
diagnostic
Moreover,
subtypes
emerging
targeted
tools,
highlighting
clinical
significance.
The
need
non-invasive
biomarkers
to
monitor
biological
processes
purposes
remains
unfulfilled.
Tapping
unique
composition
could
unlock
advanced
avenues
future.
In
this
review,
we
discuss
detail
conditions,
cancers
(encompassing
head
neck,
lung,
gastric,
breast,
hepatocellular
carcinoma),
neurodegenerative
disorders,
diabetes,
viral
infections,
autoimmune
renal
diseases,
emphasizing
advancements
molecular
diagnostics
delivery.
International Journal of Molecular Sciences,
Год журнала:
2020,
Номер
21(21), С. 8011 - 8011
Опубликована: Окт. 28, 2020
The
immune
system
plays
a
critical
role
in
protecting
hosts
from
the
invasion
of
organisms.
CD4
T
cells,
as
key
component
system,
are
central
orchestrating
adaptive
responses.
After
decades
investigation,
five
major
helper
cell
(Th)
subsets
have
been
identified:
Th1,
Th2,
Th17,
Treg
(T
regulatory),
and
Tfh
(follicular
helper)
cells.
Th1
defined
by
expression
lineage
cytokine
interferon
(IFN)-γ
master
transcription
factor
T-bet,
participate
type
1
responses
to
intracellular
pathogens
such
mycobacterial
species
viruses;
Th2
cytokines
interleukin
(IL)-4/IL-5/IL-13
GAΤA3,
2
larger
extracellular
helminths;
Th17
IL-17/IL-22
RORγt,
3
including
some
bacteria
fungi;
producing
IL-21
expressing
Bcl6,
help
B
cells
produce
corresponding
antibodies;
whereas
Foxp3-expressing
unlike
Th1/Th2/Th17/Tfh
exerting
their
effector
functions,
regulate
maintain
homeostasis
prevent
immunopathology.
Interestingly,
innate
lymphoid
(ILCs)
found
mimic
functions
three
(Th1,
Th17)
thus
can
also
be
divided
into
subsets:
ILC1s,
ILC2s,
ILC3s.
In
this
review,
we
will
discuss
differentiation
each
subset
context
ILCs
human
diseases
associated
with
dysregulation
these
lymphocyte
particularly
caused
monogenic
mutations.
Experimental Dermatology,
Год журнала:
2020,
Номер
29(8), С. 703 - 725
Опубликована: Июль 18, 2020
Anagen
stage
hair
follicles
(HFs)
exhibit
"immune
privilege
(IP)"
from
the
level
of
bulge
downwards
to
bulb.
Both
passive
and
active
IP
mechanisms
protect
HFs
physiologically
undesired
immune
responses
limit
surveillance.
is
relative,
not
absolute,
primarily
based
on
absent,
or
greatly
reduced,
intra-follicular
antigen
presentation
via
MHC
class
I
II
molecules,
along
with
prominent
expression
"no
danger"
signals
like
CD200
creation
an
immunoinhibitory
signalling
milieu
generated
by
secretory
activities
HFs.
Perifollicular
mast
cells,
Tregs
other
immunocytes
may
also
contribute
HF
maintenance
in
healthy
human
skin.
Collapse
anagen
bulb
essential
prerequisite
for
development
alopecia
areata
(AA).
In
AA,
lesional
are
rapidly
infiltrated
NKG2D
+
T
cells
natural
killer
(NK)
while
perifollicular
acquire
a
profoundly
pro-inflammatory
phenotype
interact
autoreactive
CD8+
cells.
Using
animal
models,
significant
functional
evidence
has
accumulated
that
demonstrates
dominance
system
AA
pathogenesis.
Purified
CD8+T-cell
NK
cell
populations
alone,
which
secrete
fγ,
suffice
induce
phenotype,
CD4+T-cells
aggravate
it,
iNKT
provide
relative
protection
against
development.
While
collapse
be
induced
exogenous
agents,
inherent
deficiencies
might
confer
increased
susceptibility
some
individuals.
Thus,
key
goal
effective
management
re-establishment
IP,
will
superior
disease
relapse.