Signal Transduction and Targeted Therapy,
Journal Year:
2023,
Volume and Issue:
8(1)
Published: Nov. 27, 2023
Abstract
Psoriasis
is
a
common,
chronic,
and
inflammatory
skin
disease
with
high
burden
on
individuals,
health
systems,
society
worldwide.
With
the
immunological
pathologies
pathogenesis
of
psoriasis
becoming
gradually
revealed,
therapeutic
approaches
for
this
have
gained
revolutionary
progress.
Nevertheless,
mechanisms
less
common
forms
remain
elusive.
Furthermore,
severe
adverse
effects
recurrence
upon
treatment
cessation
should
be
noted
addressed
during
treatment,
which,
however,
has
been
rarely
explored
integration
preliminary
findings.
Therefore,
it
crucial
to
comprehensive
understanding
behind
pathogenesis,
which
might
offer
new
insights
research
lead
more
substantive
progress
in
expand
clinical
options
treatment.
In
review,
we
looked
briefly
introduce
epidemiology,
subtypes,
pathophysiology,
comorbidities
systematically
discuss
signaling
pathways
involving
extracellular
cytokines
intracellular
transmission,
as
well
cross-talk
between
them.
discussion,
also
paid
attention
potential
metabolic
epigenetic
molecular
mechanistic
cascades
related
its
comorbidities.
This
review
outlined
current
psoriasis,
especially
targeted
therapies
novel
strategies,
mechanism
recurrence.
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
Journal of Hematology & Oncology,
Journal Year:
2024,
Volume and Issue:
17(1)
Published: April 29, 2024
Abstract
Hepatocellular
carcinoma
(HCC)
is
a
major
health
concern
worldwide,
with
limited
therapeutic
options
and
poor
prognosis.
In
recent
years,
immunotherapies
such
as
immune
checkpoint
inhibitors
(ICIs)
have
made
great
progress
in
the
systemic
treatment
of
HCC.
The
combination
treatments
based
on
ICIs
been
trend
this
area.
Recently,
dual
blockade
durvalumab
plus
tremelimumab
has
also
emerged
an
effective
for
advanced
However,
majority
HCC
patients
obtain
benefits.
Understanding
immunological
rationale
exploring
novel
ways
to
improve
efficacy
immunotherapy
drawn
much
attention.
review,
we
summarize
latest
area,
ongoing
clinical
trials
immune-based
therapies,
well
strategies
chimeric
antigen
receptor
T
cells,
personalized
neoantigen
vaccines,
oncolytic
viruses,
bispecific
antibodies.
Nature Communications,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: May 10, 2024
Abstract
As
a
strategy
to
improve
the
therapeutic
success
of
chimeric
antigen
receptor
T
cells
(CART)
directed
against
solid
tumors,
we
here
test
combinatorial
use
CART
and
IMSA101,
newly
developed
stimulator
interferon
genes
(STING)
agonist.
In
two
syngeneic
tumor
models,
improved
overall
survival
is
observed
when
mice
are
treated
with
intratumorally
administered
IMSA101
in
addition
intravenous
infusion.
Transcriptomic
analyses
isolated
from
tumors
show
elevated
cell
activation,
as
well
upregulated
cytokine
pathway
signatures,
particular
IL-18,
combination
treatment
group.
Also,
higher
levels
IL-18
serum
detected
treatment.
Consistent
this,
negative
impair
anti-tumor
responses
receiving
summary,
find
that
enhances
function
which
facilitated
through
STING
agonist-induced
secretion.
Molecular Cancer,
Journal Year:
2024,
Volume and Issue:
23(1)
Published: Aug. 20, 2024
Gastric
cancer
(GC)
is
one
of
the
deadliest
malignant
tumors
with
unknown
pathogenesis.
Due
to
its
treatment
resistance,
high
recurrence
rate,
and
lack
reliable
early
detection
techniques,
a
majority
patients
have
poor
prognosis.
Therefore,
identifying
new
tumor
biomarkers
therapeutic
targets
essential.
This
review
aims
provide
fresh
insights
into
enhancing
prognosis
GC
by
summarizing
processes
through
which
microRNAs
(miRNAs)
regulate
microenvironment
(TME)
highlighting
their
critical
role
in
TME.
A
comprehensive
literature
was
conducted
focusing
on
interactions
among
cells,
extracellular
matrix,
blood
vessels,
cancer-associated
fibroblasts,
immune
cells
within
The
noncoding
RNAs,
known
as
miRNAs,
modulating
TME
various
signaling
pathways,
cytokines,
growth
factors,
exosomes
specifically
examined.
Tumor
formation,
metastasis,
therapy
are
significantly
influenced
miRNAs
progression
these
multiple
exosomes.
Dysregulation
affects
cellular
such
cell
proliferation,
differentiation,
angiogenesis,
contributing
pathogenesis
GC.
play
crucial
regulation
TME,
influencing
patient
By
understanding
mechanisms
control
potential
can
be
identified
improve
PubMed,
Journal Year:
2025,
Volume and Issue:
50(2), P. 61 - 68
Published: Feb. 1, 2025
T-cell-mediated
immunity
is
essential
for
controlling
severe
acute
respiratory
syndrome
coronavirus
2
(SARSCoV2)
infection,
preventing
disease,
and
potentially
reducing
the
risk
of
long-term
disease
(COVID).
This
study
investigated
impact
natural
vaccination,
hybrid
on
T-cell
responses,
with
a
particular
emphasis
role
memory
T-cells
in
COVID-19.
The
present
reviewed
current
literature
including
development,
individuals
SARS-CoV-2
those
vaccinated
messenger
RNA
(mRNA)
vaccines,
immunity.
It
examined
studies
that
compared
activity,
immune
regulation,
prevalence
COVID-19
across
these
groups.
Natural
infection
induces
variable
cases
showing
stronger
but
sometimes
dysregulated
immunological
which
may
contribute
to
prolonged
Vaccination,
particularly
mRNA
elicits
targeted
consistent
T-cells,
severity,
incidence
Hybrid
combines
provides
most
robust
protection,
enhanceds
reduces
through
balanced
regulation.
Memory
play
critical
mitigating
Vaccination
significantly
enhances
immunity,
minimizing
chronic
symptoms
alone.
effective
defense,
emphasizing
importance
even
after
prevent
Cell Reports Medicine,
Journal Year:
2024,
Volume and Issue:
5(5), P. 101516 - 101516
Published: April 15, 2024
Non-small
cell
lung
cancer
(NSCLC)
is
known
for
high
relapse
rates
despite
resection
in
early
stages.
Here,
we
present
the
results
of
a
phase
I
clinical
trial
which
dendritic
(DC)
vaccine
targeting
patient-individual
neoantigens
evaluated
patients
with
resected
NSCLC.
Vaccine
manufacturing
feasible
six
10
enrolled
patients.
Toxicity
limited
to
grade
1-2
adverse
events.
Systemic
T
responses
are
observed
five
out
vaccinated
patients,
remaining
detectable
up
19
months
post
vaccination.
Single-cell
analysis
indicates
that
responsive
population
polyclonal
and
exhibits
near-entire
spectrum
differentiation
states,
including
naive-like
state,
but
excluding
exhausted
states.
Three
experience
disease
recurrence
during
follow-up
period
2
years.
Collectively,
these
data
support
feasibility,
safety,
immunogenicity
this
treatment