Korean Journal of Gastroenterology,
Journal Year:
2024,
Volume and Issue:
84(2), P. 51 - 64
Published: Aug. 23, 2024
Small
molecules,
including
Janus
kinase
(JAK)
inhibitors
and
sphingosine-1-phosphate
receptor
modulators
(S1PRMs),
are
promising
new
treatments
for
inflammatory
bowel
disease
(IBD).
molecules
exhibit
more
predictable
pharmacokinetics
than
biologics,
less
likely
to
induce
immune
responses,
can
be
administered
orally.
JAK
function
by
blocking
the
activity
of
enzymes,
which
prevents
subsequent
phosphorylation
activation
signal
transducer
activator
transcription
(STAT)
proteins.
Tofacitinib
filgotinib
approved
treating
ulcerative
colitis
(UC),
while
upadacitinib
is
UC
Crohn's
disease.
Nevertheless,
increase
risk
herpes
zoster,
cancer,
major
adverse
cardiovascular
events,
venous
thromboembolism.
S1PRMs
bind
S1PRs,
particularly
S1PR1,
on
lymphocytes.
This
interaction
inhibits
lymphocytes
from
exiting
lymph
nodes
migrating
gut,
thereby
reducing
inflammation
response
in
intestinal
mucosa.
Ozanimod
etrasimod
treatment
UC,
but
they
cause
side
effects
such
as
bradycardia,
conduction
disorder,
macular
edema.
Overall,
offer
significant
benefits
managing
IBD,
although
their
potential
require
careful
monitoring.
Frontiers in Psychiatry,
Journal Year:
2024,
Volume and Issue:
15
Published: June 24, 2024
Autism
spectrum
disorder
(ASD
1
)
is
a
behaviorally
defined
syndrome
encompassing
markedly
heterogeneous
patient
population.
Many
ASD
subjects
fail
to
respond
the
st
line
behavioral
and
pharmacological
interventions,
leaving
parents
seek
out
other
treatment
options.
Evidence
supports
that
neuroinflammation
plays
role
in
pathogenesis.
However,
underlying
mechanisms
likely
vary
for
each
patient,
influenced
by
genetic,
epigenetic,
environmental
factors.
Although
anti-inflammatory
measures,
mainly
based
on
metabolic
changes
oxidative
stress,
have
provided
promising
results
some
subjects,
use
of
such
measures
requires
careful
selection
clinical
laboratory
findings.
Recent
progress
neuroscience
molecular
immunology
has
made
it
possible
allow
re-purposing
currently
available
medications,
used
autoimmune
chronic
inflammatory
conditions,
as
options
subjects.
On
hand,
emerging
including
biologic
gate-keeper
blockers,
exert
powerful
effects
specific
mediators
or
signaling
pathways.
It
will
require
both
keen
understanding
action
agents
patients
suitable
treatment.
This
review
attempt
summarize
already
targeting
patients,
then
applicable
scientific
rationale
trial
data,
if
available.
In
our
experience,
were
treated
under
diagnoses
autoimmune/autoinflammatory
conditions
and/or
post-infectious
neuroinflammation.
there
are
little
data
specifically
Therefore,
these
immunomodulating
potential
be
discussed
preclinical
case
reports,
generated
with
medical
conditions.
hopefully
highlight
expanding
scope
treating
Expert Opinion on Pharmacotherapy,
Journal Year:
2024,
Volume and Issue:
25(6), P. 655 - 672
Published: April 12, 2024
Pruritus,
particularly
in
its
chronic
form,
often
imposes
significant
suffering
and
reductions
patients'
quality
of
life.
The
pathophysiology
itch
is
varied
depending
on
disease
context,
creating
opportunities
for
unique
drug
development
multimodal
therapy.
Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: Nov. 8, 2024
The
limited
therapeutic
options
and
inconsistent
treatment
efficacy
of
Intestinal
Behçet's
disease
complicate
its
management,
with
the
absence
standardized
guidelines
further
exacerbating
challenges
faced
by
clinicians.
Korean Journal of Gastroenterology,
Journal Year:
2024,
Volume and Issue:
84(2), P. 51 - 64
Published: Aug. 23, 2024
Small
molecules,
including
Janus
kinase
(JAK)
inhibitors
and
sphingosine-1-phosphate
receptor
modulators
(S1PRMs),
are
promising
new
treatments
for
inflammatory
bowel
disease
(IBD).
molecules
exhibit
more
predictable
pharmacokinetics
than
biologics,
less
likely
to
induce
immune
responses,
can
be
administered
orally.
JAK
function
by
blocking
the
activity
of
enzymes,
which
prevents
subsequent
phosphorylation
activation
signal
transducer
activator
transcription
(STAT)
proteins.
Tofacitinib
filgotinib
approved
treating
ulcerative
colitis
(UC),
while
upadacitinib
is
UC
Crohn's
disease.
Nevertheless,
increase
risk
herpes
zoster,
cancer,
major
adverse
cardiovascular
events,
venous
thromboembolism.
S1PRMs
bind
S1PRs,
particularly
S1PR1,
on
lymphocytes.
This
interaction
inhibits
lymphocytes
from
exiting
lymph
nodes
migrating
gut,
thereby
reducing
inflammation
response
in
intestinal
mucosa.
Ozanimod
etrasimod
treatment
UC,
but
they
cause
side
effects
such
as
bradycardia,
conduction
disorder,
macular
edema.
Overall,
offer
significant
benefits
managing
IBD,
although
their
potential
require
careful
monitoring.