Cell Reports,
Journal Year:
2024,
Volume and Issue:
43(9), P. 114681 - 114681
Published: Aug. 24, 2024
Regulatory
T
cells
(Tregs)
suppress
pro-inflammatory
conventional
cell
(Tconv)
responses.
As
lipids
impact
signaling
and
function,
we
compare
the
lipid
composition
of
CD4
Molecular Neurodegeneration,
Journal Year:
2024,
Volume and Issue:
19(1)
Published: April 5, 2024
Ageing
is
the
principal
risk
factor
for
retinal
degenerative
diseases,
which
are
commonest
cause
of
blindness
in
developed
countries.
These
conditions
include
age-related
macular
degeneration
or
diabetic
retinopathy.
Regulatory
T
cells
play
a
vital
role
immunoregulation
nervous
system
by
limiting
inflammation
and
tissue
damage
health
disease.
Because
retina
was
long-considered
an
immunoprivileged
site,
precise
contribution
regulatory
homeostasis
diseases
remains
unknown.
CD4
+
CD25
Foxp3
regulatory
T
cells
(Treg)
have
been
implicated
in
pain
modulation
various
inflammatory
conditions.
However,
whether
Treg
hamper
at
steady
state
and
by
which
mechanism
is
still
unclear.
From
a
meta-analysis
of
the
transcriptomes
murine
conventional
(Tconv),
we
observe
that
proenkephalin
gene
(
Penk
),
encoding
precursor
analgesic
opioid
peptides,
ranks
among
top
25
genes
most
enriched
cells.
We
then
present
evidence
suggesting
regulated
part
members
Tumor
Necrosis
Factor
Receptor
(TNFR)
family
transcription
factor
Basic
leucine
zipper
faatf-like
(BATF).
Using
mice
promoter
activity
can
be
tracked
with
fluorescent
reporter,
also
show
expression
mostly
detected
activated
Tconv
non-inflammatory
conditions
colon
skin.
Functionally,
proficient
or
deficient
for
suppress
equally
well
proliferation
effector
vitro
autoimmune
colitis
vivo.
In
contrast,
inducible
ablation
leads
to
heat
hyperalgesia
both
male
female
mice.
Overall,
our
results
indicate
might
play
key
role
modulating
basal
somatic
sensitivity
through
production
peptides.
Transplantation,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 9, 2025
Tissue-resident
lymphocytes
(TRLs)
provide
a
front-line
immunological
defense
mechanism
uniquely
placed
to
detect
perturbations
in
tissue
homeostasis.
The
heterogeneous
TRL
population
spans
the
innate
adaptive
immune
continuum,
with
roles
during
normal
physiology
homeostatic
maintenance,
repair,
pathogen
detection,
and
rapid
mounting
of
responses.
TRLs
are
especially
enriched
liver,
every
subset
represented,
including
liver-resident
natural
killer
cells;
tissue-resident
memory
B
conventional
CD8,
CD4,
regulatory
T
unconventional
gamma-delta,
killer,
mucosal-associated
invariant
cells.
importance
donor-
recipient-derived
after
transplantation
is
becoming
increasingly
recognized,
although
it
has
not
been
examined
detail
liver
transplantation.
This
review
summarizes
evidence
for
transplant
immunology,
focusing
on
their
features,
functions,
potential
harnessing
improve
outcomes.
PLoS Pathogens,
Journal Year:
2025,
Volume and Issue:
21(1), P. e1012906 - e1012906
Published: Jan. 30, 2025
Tissue-repair
regulatory
T
cells
(trTregs)
comprise
a
specialized
cell
subset
essential
for
tissue
homeostasis
and
repair.
While
well-studied
in
sterile
injury
models,
their
role
infection-induced
damage
antimicrobial
immunity
is
less
understood.
We
investigated
trTreg
dynamics
during
acute
Trypanosoma
cruzi
infection,
marked
by
extensive
strong
CD8+
immunity.
Unlike
trTregs
significantly
declined
secondary
lymphoid
organs
non-lymphoid
target
tissues
correlating
with
systemic
local
damage,
downregulation
of
function-associated
genes
skeletal
muscle.
This
decline
was
linked
to
decreased
IL-33
levels,
key
growth
factor,
promoted
the
Th1
cytokine
IFN-γ.
Early
recombinant
treatment
increased
trTregs,
type
2
innate
cells,
parasite-specific
at
specific
time
points
after
leading
reduced
lower
parasite
burden,
improved
disease
outcome.
Our
findings
not
only
provide
novel
insights
into
infection
but
also
highlight
potential
optimizing
immune
balance
modulating
responses
promote
repair
while
maintaining
effective
pathogen
control
injury.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: March 6, 2025
Tissue
resident
regulatory
T
cells
(tissue
Tregs)
are
vital
for
maintaining
immune
homeostasis
and
controlling
inflammation.
They
aid
in
repairing
damaged
tissues
influencing
the
progression
of
fibrosis.
However,
despite
extensive
research
on
how
tissue
Tregs
interact
with
non-immune
during
repair,
their
pro-
anti-fibrotic
effects
chronic
injury
remain
unclear.
Understanding
various
cell
types,
as
well
roles
fibrosis,
is
crucial
uncovering
mechanisms
behind
these
conditions.
In
this
review,
we
describe
repair
fibrosis
across
different
explore
potential
strategies
regulating
homeostasis.
These
insights
hold
promise
providing
new
perspectives
approaches
treatment
irreversible
fibrotic
diseases.
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 15, 2025
Abstract
In
colorectal
cancer
(CRC),
tumor-infiltrating
regulatory
T
(Treg)
cells
suppress
anti-tumor
immunity,
promoting
immune
evasion
and
tumor
progression.
Effective
therapies
require
selectively
targeting
Treg
(TI-Treg)
while
preserving
systemic
cells,
necessitating
insight
into
their
adaptations
within
the
microenvironment.
Here,
CRC-organoids
were
implanted
in
liver
of
Foxp3eGFP
mice
to
investigate
location-specific
phenotypic
differences
TI-Treg
cells.
Tumor
tissue
exhibited
an
increased
proportion
a
decrease
effector
CD4⁺
CD8⁺
compared
matched
healthy
tissue.
RNA
sequencing
isolated
from
spleen,
primary
transplant,
or
metastases
identified
gene
expression
profiles
previously
associated
with
CRC-related
patients.
Location-specific
included
elevated
WNT-pathway
genes
peritoneal
counterparts.
Higher
upregulated
correlated
poor
CRC
prognosis.
Splenic
tumor-bearing
displayed
distinct
transcriptional
both
counterparts
suggesting
they
represent
CD4
+
population.
Taken
together,
these
findings
highlight
heterogeneity
across
different
sites
nature
splenic
hosts.