IL-23 Promotes γδT Cell Activity in Dry Eye Disease Progression
Yanxiao Li,
No information about this author
Zan Luo,
No information about this author
Zihao Liu
No information about this author
et al.
Investigative Ophthalmology & Visual Science,
Journal Year:
2025,
Volume and Issue:
66(2), P. 10 - 10
Published: Feb. 4, 2025
Purpose:
Conjunctival-resident
γδT
cells,
the
predominant
ocular
source
of
interleukin-17A
(IL-17A),
play
crucial
roles
in
dry
eye
disease
(DED)
pathogenesis.
The
upstream
regulators
these
cells
are
unknown.
This
study
evaluated
role
conjunctival
IL-23
expression
mediating
cell
generation
and
elucidated
its
contribution
to
inflammatory
responses.
Methods:
Single-cell
RNA
sequencing
(scRNA-seq)
was
used
identify
quantify
mRNA
molecules
mice.
level
increased
wild-type
(WT)
decreased
γδT-deficient
(TCRδ–/–)
mice
after
induced
via
an
intelligently
controlled
environmental
system
(ICES).
Flow
cytometry
transcriptome
were
investigate
impact
changes
on
human
cells.
Results:
receptor
(IL-23R)
greater
than
other
types,
such
as
CD4+
T
CD8+
epithelial
An
increase
led
density,
which
proportional
severity.
However,
TCRδ–/–
mice,
upregulation
failed
IL-17A
severity
eye.
Furthermore,
increases
number
evident
surface
patients
who
developed
visual
display
terminal
syndrome.
Conclusions:
contributes
induction
DED
response
through
interactions
with
cognate
promotion
their
proliferation.
findings
this
suggest
that
suppression
blockade
IL-23R
activation
may
be
a
viable
target
for
improving
management
inflammation
patients.
Language: Английский
Comprehensive biomarker profiles in hematological malignancies: improving diagnosis, prognosis, and treatment
Biomarkers in Medicine,
Journal Year:
2025,
Volume and Issue:
unknown, P. 1 - 16
Published: Feb. 27, 2025
Hematological
malignancies
present
substantial
challenges
in
clinical
practice
due
to
their
heterogeneity
and
complex
biological
profiles.
In
these
diseases,
biomarkers
–
measurable
indicators
of
states
are
indispensable
for
diagnosis,
prognosis,
therapeutic
decision-making.
Emerging
significantly
improving
outcomes
hematological
cancers
by
enhancing
early
detection,
refining
prognostic
assessments,
enabling
personalized
treatment
approaches,
optimizing
overall
patient
management.
This
progress
translates
into
better
more
effective
strategies
treat
manage
malignancies.
The
field
biomarker
discovery
has
developed
from
basic
morphological
cytogenetic
markers
advanced
molecular
techniques,
including
polymerase
chain
reaction
(PCR)
next-generation
sequencing
(NGS),
which
have
enhanced
diagnostic
accuracy
led
the
development
targeted
therapies.
Additionally,
recent
advent
technologies
like
mass
spectrometry
single-cell
RNA
enables
comprehensive
profiling
reveals
novel
that
were
previously
undetectable.
Our
aim
this
manuscript
is
provide
a
overview
immunohematological
biomarkers,
applications,
future
directions
field.
Language: Английский
Prognostic value of natural killer T cell related genes in acute myeloid leukemia
Qiong Liu,
No information about this author
Zhaona Zhou,
No information about this author
Ping Xu
No information about this author
et al.
Cancer Cell International,
Journal Year:
2025,
Volume and Issue:
25(1)
Published: April 13, 2025
Acute
myeloid
leukemia
(AML)
is
a
hematological
malignancy
characterized
by
complex
immune
microenvironment.
This
study
aims
to
identify
immune-related
prognostic
biomarkers
in
AML.
Multiple
public
sequencing
datasets
were
utilized
analyze
differentially
expressed
genes
(DEGs)
Single-sample
gene
set
enrichment
analysis
(ssGSEA)
and
weighted
co-expression
network
(WGCNA)
also
performed.
Immune
cell
infiltration
was
assessed
at
the
single-cell
level.
NKT
marker
intersected
with
most
AML-relevant
module
key
genes.
Prognostic
screened
using
Cox
Lasso
regression
model,
their
value
evaluated
random
forest
Kaplan-Meier
survival
analyses.
Gene
expression
validated
RT-qPCR
Western
blot,
levels
analyzed
flow
cytometry.
A
total
of
1,919
common
DEGs
obtained
between
AML
controls.
WGCNA
revealed
that
brown
strongly
associated
Single-cell
showed
significantly
reduced
patients,
consistent
ssGSEA
results.
Forty
intersecting
identified
10
(FGFBP2,
GZMB,
GZMH,
IKZF3,
IL2RB,
KLRB1,
KLRC2,
RHOF,
RUNX3,
STAT4).
risk
score
model
based
on
these
stratified
patients
into
high-risk
low-risk
groups,
significant
differences
prognosis
two
groups.
blot
analyses
downregulated
patients.
Flow
cytometry
results
lower
CD8
+
T
cells
compared
highlighted
critical
role
pathogenesis.
The
provides
new
insights
potential
for
understanding
biology,
prognosis,
therapeutic
targets.
Language: Английский
Advances in DNA/RNA Sequencing and Their Applications in Acute Myeloid Leukemia (AML)
Fatimah O. Ahmed,
No information about this author
Jiang F. Zhong
No information about this author
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
26(1), P. 71 - 71
Published: Dec. 25, 2024
Acute
myeloid
leukemia
(AML)
is
an
aggressive
malignancy
that
poses
significant
challenges
due
to
high
rates
of
relapse
and
resistance
treatment,
particularly
in
older
populations.
While
therapeutic
advances
have
been
made,
survival
outcomes
remain
suboptimal.
The
evolution
DNA
RNA
sequencing
technologies,
including
whole-genome
(WGS),
whole-exome
(WES),
(RNA-Seq),
has
significantly
enhanced
our
understanding
AML
at
the
molecular
level.
These
technologies
led
discovery
driver
mutations
transcriptomic
alterations
critical
for
improving
diagnosis,
prognosis,
personalized
therapy
development.
Furthermore,
single-cell
(scRNA-Seq)
uncovered
rare
subpopulations
stem
cells
(LSCs)
contributing
disease
progression
relapse.
However,
widespread
clinical
integration
these
tools
remains
limited
by
costs,
data
complexity,
ethical
challenges.
This
review
explores
recent
advancements
DNA/RNA
highlights
both
potential
limitations
techniques
practice.
Language: Английский