Experiments in Fluids,
Journal Year:
2024,
Volume and Issue:
65(8)
Published: July 17, 2024
Abstract
Traumatic
brain
injury
(TBI)
poses
a
major
public
health
challenge.
No
proven
therapies
for
the
condition
exist
so
protective
equipment
that
prevents
or
mitigates
these
injuries
plays
critical
role
in
minimizing
societal
burden
of
this
condition.
Our
ability
to
optimize
depends
on
our
capacity
relate
mechanics
head
impact
events
morbidity
and
mortality.
This
capacity,
turn,
correctly
identifying
mechanisms
injury.
For
several
decades,
controversial
theory
TBI
biomechanics
has
attributed
important
classes
cavitation
inside
cranial
vault
during
blunt
impact.
explains
counter-intuitive
clinical
observations,
including
coup–contre-coup
pattern
However,
it
is
also
difficult
validate
experimentally
living
subjects.
Also,
broad
term
covers
range
different
events,
some
which
may
be
better
described
by
than
others.
review
surveys
what
been
learned
about
through
mathematical
modeling,
physical
experimentation
with
tissues
places
context
competing
theories
recent
research
activity
field
an
attempt
understand
offer
next
generation
innovators
biomechanics.
The Lancet Regional Health - Europe,
Journal Year:
2024,
Volume and Issue:
44, P. 101011 - 101011
Published: July 25, 2024
Immune
checkpoint
inhibitor-related
encephalitis
(ICI-encephalitis)
is
not
well
characterised
and
diagnostic
prognostic
biomarkers
are
lacking.
We
aimed
to
comprehensively
characterise
ICI-encephalitis
identify
outcome
predictors.
Current Opinion in Neurology,
Journal Year:
2024,
Volume and Issue:
37(3), P. 345 - 352
Published: March 14, 2024
Purpose
of
review
Immune
checkpoint
inhibitors
(ICI)
may
trigger
immune-related
adverse
events
which
rarely
affect
the
central
nervous
system
(CNS-irAEs).
Over
past
few
years,
cumulative
data
have
led
to
characterization
well
defined
syndromes
with
distinct
cancer
and
antibody
associations
as
different
outcomes.
Recent
findings
The
most
frequent
CNS-irAE
is
encephalitis,
includes
three
main
groups:
meningoencephalitis,
a
nonfocal
syndrome
usually
responsive
corticosteroids;
limbic
associated
high-risk
paraneoplastic
neurological
(PNS)
antibodies
(e.g.
anti-Hu,
anti-Ma2)
neuroendocrine
cancers,
characterized
by
poor
treatment
response
outcomes;
cerebellar
ataxia,
variable
outcomes
(worse
when
PNS
are
detected).
Additionally,
diffuse
encephalopathy
without
inflammatory
findings,
corticosteroids
high
mortality
has
been
described.
spectrum
CNS-irAEs
also
meningitis,
myelitis,
rarer
presentations.
A
subset
(i.e.
encephalitis
and/or
rapidly
progressive
ataxia)
undistinguishable
from
ICI-naïve
PNS.
Summary
clinical
diversity
suggests
pathogenic
mechanisms,
need
be
understood
establish
more
effective
specific
modalities.
It
crucial
identify
biomarkers
able
predict
patients
will
experience
severe
CNS-irAEs,
anticipate
their
diagnosis,
long-term
International Journal of Cancer,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 20, 2025
Abstract
Neurologic
immune‐related
adverse
events
(nirAEs)
represent
rare,
yet
severe
side
effects
associated
with
immune
checkpoint
inhibitor
(ICI)
therapy.
Given
the
absence
of
established
diagnostic
biomarkers
for
nirAEs,
we
aimed
to
evaluate
utility
serum
Neurofilament
Light
Chain
(NfL)
and
Glial
Fibrillary
Acidic
Protein
(GFAP).
Fifty‐three
patients
were
included
at
three
comprehensive
cancer
centers,
these
20
manifest
nirAEs
11
irHypophysitis.
Controls
without
any
irAE
(
n
=
8)
other
irAEs
14).
Using
a
single‐molecule
enzyme‐linked
immunosorbent
assay
(Simoa),
levels
measured
prior
to,
during
after
manifestation
(n)irAEs
in
80
samples.
Symptom
severity
was
graded
according
Common
Criteria
Adverse
Events
(CTCAE)
version
5.0.
Serum
NfL
significantly
higher
nirAE
group
20)
compared
irHypophysitis
11;
p
.0025)
controls
22;
.0384).
Subgroup
analysis
demonstrated
significant
elevation
peripheral
nerves
(PNirAE)
contrast
neuromuscular
syndromes
(NMirAE)
.0260).
GFAP
highest
affecting
central
nervous
system
(CNSirAE)
PNirAE
NMirAE
.0064).
increased
.0069,
.0092).
Individuals
elevated
exhibited
less
favorable
outcomes
.0199).
Measurement
may
be
helpful
differentiation
broad
spectrum
serve
as
an
indicator
symptom
severity.
Further
investigation
is
needed
their
potential
prognostic
biomarkers.
Frontiers in Molecular Biosciences,
Journal Year:
2025,
Volume and Issue:
12
Published: Feb. 4, 2025
Intracerebral
hemorrhage
(ICH)
is
a
non
traumatic
that
occurs
in
certain
part
of
the
brain.
It
usually
leads
to
brain
cell
damage.
According
large
number
experimental
research,
oxidative
stress
an
important
pathophysiological
processes
cerebral
hemorrhage.
In
this
paper,
we
aim
determine
how
changes
biomarkers
indicate
damage
degree
hemorrhage,
and
explore
summarize
potential
treatments
or
interventions.
We
found
patients
with
are
characterized
by
increased
levels
markers,
such
as
total
malondialdehyde
(MDA),
F2
isoprostaglandin,
hydroxynonenal,
myeloperoxidase
protein
hydroxyl.
Therefore,
caused
ICH
on
these
markers
can
be
used
evaluate
diagnose
ICH,
predict
its
prognosis,
guide
preventive
treatment
turn
antioxidant
based
new
alternative.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: March 13, 2025
Cancer
immunotherapy
with
immune
checkpoint
inhibitors
(ICIs)
has
revolutionized
oncology,
significantly
improving
survival
across
multiple
cancer
types.
ICIs,
such
as
anti-PD-1
(e.g.
nivolumab,
pembrolizumab),
anti-PD-L1
atezolizumab,
avelumab),
and
anti-CTLA-4
ipilimumab),
enhance
T
cell-mediated
anti-tumor
responses
but
can
also
trigger
immune-related
adverse
events
(irAEs).
Neurological
irAEs
(n-irAEs),
affecting
1-3%
of
patients,
predominantly
involve
the
peripheral
nervous
system;
less
commonly,
n-irAEs
present
central
system
disorders.
Although
suggest
a
possible
correlation
treatment
efficacy,
their
mechanisms
remain
unclear,
hypotheses
ranging
from
antigen
mimicry
to
cytokine
dysregulation
microbiome
alterations.
Identifying
patients
at
risk
for
predicting
outcome
through
biomarkers
would
be
highly
desirable.
For
example,
high-risk
onconeural
antibodies
(such
anti-Hu
or
Ma2),
elevated
neurofilament
light
chain
(NfL)
levels
often
respond
poorly
irAE
treatment.
However,
interpreting
neuronal
antibody
tests
in
diagnosis
requires
caution:
positive
results
must
align
clinical
context,
some
(e.g.,
SCLC)
may
have
asymptomatic
low
levels,
false
are
common
without
tissue-based
confirmation.
Also,
use
IL-6)
lead
more
targeted
treatments
irAEs,
minimizing
effects
compromising
efficacy
ICIs.
This
review
provides
comprehensive
overview
latest
findings
on
associated
focus
prediction,
prevention,
well
precision
using
autoantibodies,
cytokines,
microbiota.
The
most
interesting
data
concern
antibodies,
which
we
explore
pathogenic
roles
neurotoxicity.
Most
available
both
regarding
role
diagnostic
prognostic
supporting
therapeutic
decisions
toxicities,
refer
non-neurological
toxicities.
our
review,
mention
potential
CXCL10
CXCL13
describe
current
evidence,
need
further
studies,
cytokines
guiding
selection
second-line
therapies
n-irAEs.
Finally,
no
specific
microbiome-related
microbial
signature
been
proven
linked
specifically,
leading
future
research
topic.
Cell Death and Disease,
Journal Year:
2025,
Volume and Issue:
16(1)
Published: March 29, 2025
Intracerebral
hemorrhage
(ICH)
is
a
severe
stroke
subtype
with
high
mortality
and
disability
rates,
long-term
outcomes
among
survivors
remain
unpredictable
due
to
the
lack
of
reliable
biomarkers.
In
this
study,
spatial
transcriptomics
was
used
analyze
molecular
profiles
in
autopsy
brain
tissues
from
chronic
ICH
patients,
revealing
distinct
transcriptomic
features
thalamus
cortex,
common
inflammatory
characteristics
such
as
gliosis,
apoptosis,
immune
activation.
Serine
proteinase
inhibitor
NA3
(SERPINA3)
significantly
upregulated
both
regions
co-expressed
astrocytes
thalamus.
Pathological
studies
postmortem
human
mouse
models
confirmed
elevated
SERPINA3
expression,
murine
Serpina3n
showing
similar
pattern
mice.
Plasma
analysis
250
patients
healthy
controls
revealed
higher
levels
correlating
severity,
National
Institutes
Health
Stroke
Scale
(NIHSS),
Glasgow
Coma
(GCS)
scores,
functional
outcomes.
Higher
within
72
hours
onset
were
independently
associated
worse
recovery
(mRS
≥
3)
increased
all-cause
at
6
12
months.
Additionally,
7
days
post-ictus
correlated
white
matter
hyperintensities
poor
cognitive
performance
These
findings
highlight
potential
prognostic
biomarker
for
ICH,
warranting
further
investigation
into
its
role
neurological
dysfunction
validation
larger
prospective
cohorts.