IntechOpen eBooks,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Aug. 20, 2024
The
role
of
inflammation
in
the
aetiopathogenesis
malignant
brain
tumours
is
increasingly
recognised.
Chronic
inflammation,
characterised
by
a
sustained
immune
response
and
tissue
remodelling,
contributes
to
development
progression
tumours.
Activated
microglia
infiltrating
cells
release
proinflammatory
cytokines
reactive
oxygen
species,
creating
neuroinflammatory
environment
that
promotes
tumour
growth.
This
persistent
leads
DNA
damage,
mutations
epigenetic
changes,
thus
favouring
malignancy.
Epidemiological
studies
have
linked
chronic
inflammatory
diseases
infections
an
increased
risk
Underlying
mechanisms
include
activating
signalling
pathways
such
as
nuclear
factor
kappa
B
(NF-κB)
signal
transducer
activator
transcription
3
(STAT3),
which
promote
cell
proliferation
survival.
In
contrast,
mediators
angiogenesis
evasion
system.
text
discusses
markers
bacterial
viral
developing
Nutrients,
Journal Year:
2025,
Volume and Issue:
17(2), P. 241 - 241
Published: Jan. 10, 2025
The
global
pandemic
of
obesity
poses
a
serious
health,
social,
and
economic
burden.
Patients
living
with
are
at
an
increased
risk
developing
noncommunicable
diseases
or
to
die
prematurely.
Obesity
is
state
chronic
low-grade
inflammation.
Neutrophils
first
be
recruited
sites
inflammation,
where
they
contribute
host
defense
via
phagocytosis,
degranulation,
extrusion
neutrophil
extracellular
traps
(NETs).
NETs
web-like
DNA
structures
nuclear
mitochondrial
associated
cytosolic
antimicrobial
proteins.
primary
function
NETosis
preventing
the
dissemination
pathogens.
However,
neutrophils
may
occasionally
misidentify
molecules
as
danger-associated
molecular
patterns,
triggering
NET
formation.
This
can
lead
further
recruitment
neutrophils,
resulting
in
propagation
vicious
cycle
persistent
systemic
scenario
occur
when
infiltrate
expanded
obese
adipose
tissue.
Thus,
implicated
pathophysiology
autoimmune
metabolic
disorders,
including
obesity.
review
explores
role
two
obesity-associated
conditions-hypertension
liver
steatosis.
With
rising
prevalence
driving
research
into
its
pathophysiology,
particularly
through
diet-induced
models
rodents,
we
discuss
insights
gained
from
both
human
animal
studies.
Additionally,
highlight
potential
offered
by
rodent
opportunities
presented
genetically
modified
mouse
strains
for
advancing
our
understanding
obesity-related
Cells,
Journal Year:
2024,
Volume and Issue:
13(14), P. 1172 - 1172
Published: July 9, 2024
Sepsis,
a
condition
characterized
by
life-threatening
organ
dysfunction
due
to
dysregulated
host
response
infection,
significantly
impacts
global
health,
with
mortality
rates
varying
widely
across
regions.
Traditional
therapeutic
strategies
that
target
hyperinflammation
and
immunosuppression
have
largely
failed
improve
outcomes,
underscoring
the
need
for
innovative
approaches.
This
review
examines
development
of
agents
sepsis,
focus
on
clinical
trials
addressing
immunosuppression.
It
highlights
frequent
failures
these
trials,
explores
underlying
reasons,
outlines
current
research
efforts
aimed
at
bridging
gap
between
theoretical
advancements
applications.
Although
personalized
medicine
phenotypic
categorization
present
promising
directions,
this
emphasizes
importance
understanding
complex
pathogenesis
sepsis
developing
targeted,
effective
therapies
enhance
patient
outcomes.
By
multifaceted
nature
future
can
pave
way
more
precise
individualized
treatment
strategies,
ultimately
improving
management
prognosis
patients.
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(13), P. 7396 - 7396
Published: July 5, 2024
Sepsis
poses
a
significant
threat
to
human
health
due
its
high
morbidity
and
mortality
rates
worldwide.
Traditional
diagnostic
methods
for
identifying
sepsis
or
causative
organisms
are
time-consuming
contribute
rate.
Biomarkers
have
been
developed
overcome
these
limitations
currently
used
diagnosis,
prognosis
prediction,
treatment
response
assessment.
Over
the
past
few
decades,
more
than
250
biomarkers
identified,
of
which
in
clinical
decision-making.
Consistent
with
diagnosing
sepsis,
there
is
no
specific
sepsis.
Currently,
general
conservative
includes
timely
antibiotic
use
hemodynamic
support.
When
planning
sepsis-specific
treatment,
it
important
select
most
suitable
patient,
considering
heterogeneous
nature
This
comprehensive
review
summarizes
current
evolving
therapeutic
approaches
International Journal of Nanomedicine,
Journal Year:
2025,
Volume and Issue:
Volume 20, P. 687 - 703
Published: Jan. 1, 2025
Background:
Exosomes
sourced
from
mesenchymal
stem
cells
(MSC-EXOs)
have
become
a
promising
therapeutic
tool
for
sepsisinduced
myocardial
dysfunction
(SMD).Our
previous
study
demonstrated
that
Apelin
pretreatment
enhanced
the
benefit
of
MSCs
in
infarction
by
improving
their
paracrine
effects.This
aimed
to
determine
whether
EXOs
Apelin-pretreated
(Apelin-MSC-EXOs)
would
potent
cardioprotective
effects
against
SMD
and
elucidate
underlying
mechanisms.Methods:
MSC-EXOs
Apelin-MSC-EXOs
were
isolated
identified.Mice
neonatal
cardiomyocytes
(NCMs)
treated
with
or
under
lipopolysaccharide
(LPS)
condition
vitro.Cardiomyocyte
pyroptosis
was
determined
TUNEL
staining.RNA
sequencing
used
identify
differentially
expressed
functional
miRNAs
between
Apelin-MSC-EXOs.MSC-EXOs
transplanted
into
mouse
model
induced
cecal
ligation
puncture
(CLP)
via
tail
vein.Heart
function
evaluated
echocardiography.Results:
Compared
MSC-EXOs,
Apelin-MSC-EXO
transplantation
greatly
cardiac
mice.Both
suppressed
cardiomyocyte
vivo
vitro,
latter
exhibiting
superior
protective
effects.miR-34a-5p
effectively
mediated
exert
high
mobility
group
box-1
(HMGB1)
as
potential
target.Mechanistically,
delivered
miR-34a-5p
injured
cardiomyocytes,
thereby
ameliorating
regulation
HMGB1/AMPK
axis.These
partially
abrogated
downregulation
Apelin-MSC-EXOs.Conclusion:
Our
revealed
key
component
protected
mediation
signaling
pathway.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: Feb. 6, 2025
Sepsis,
a
heterogeneous
illness
produced
by
dysregulated
host
response
to
infection,
remains
severe
mortality
risk.
Recent
discoveries
in
sepsis
research
have
stressed
phenotyping
as
feasible
strategy
for
tackling
heterogeneity
and
enhancing
therapy
precision.
Sepsis
has
moved
from
traditional
stratifications
based
on
severity
prognosis
dynamic,
phenotype-driven
therapeutic
options.
This
review
covers
recent
progress
connecting
subgroups
personalized
treatments,
with
focus
phenotype-based
predictions
decision-support
systems.
Despite
ongoing
challenges,
such
standardizing
frameworks
incorporating
findings
into
clinical
practice,
this
topic
enormous
promise.
By
investigating
phenotypic
variation
responses,
we
hope
uncover
new
biomarkers
solutions,
laying
the
groundwork
more
effective
therapies
and,
ultimately
improving
patient
outcomes.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: Feb. 28, 2025
Most
early
studies
investigating
the
role
of
C-reactive
protein
(CRP)
in
tissue
damage
determined
it
supported
pro-hemostatic
and
pro-inflammatory
activities.
However,
these
findings
were
not
universal,
as
other
data
suggested
CRP
inhibited
same
processes.
A
potential
explanation
for
disparate
observations
finally
emerged
with
recognition
that
undergoes
context-dependent
conformational
changes
vivo
,
each
its
three
isoforms
–
pentameric
(pCRP),
modified
(pCRP*),
monomeric
(mCRP)
have
different
effects.
In
this
review,
we
consider
new
paradigm
re-evaluate
repair
process.
Indeed,
a
growing
body
evidence
points
toward
involvement
just
hemostasis
inflammation,
but
also
resolution
inflammation
regeneration.
Additionally,
briefly
discuss
shortcomings
currently
available
diagnostic
tests
highlight
need
change
how
is
utilized
clinical
practice.
TRAUMA,
Journal Year:
2025,
Volume and Issue:
26(1), P. 1 - 10
Published: March 7, 2025
Background.
In
patients
with
injuries
of
large
joints,
the
activation
inflammation
causes
risk
thrombophilia.
The
prediction
thrombotic
complications
and
their
prevention
can
improve
quality
treatment.
purpose:
to
investigate
data
scientific
medical
literature
on
pathogenetic
association
between
markers
hemostasis
in
degenerative
diseases
post-traumatic
joints.
Materials
methods.
search
for
has
been
made
PubMed
database
10
years.
Sixty
works
were
selected.
Results.
A
total
60
papers
selected
analysis.
They
recorded
information
about
relationship
mechanisms
hypercoagulability
trauma.
specified
are
given
this
work.
Conclusions.
orthopedics
traumatology,
considerable
attention
is
paid
surgical
treatment
trauma,
particular,
Individuals
trauma
or
surgery
joints
have
a
correlation
biochemical
common
clinical
inflammation,
metabolism
glycoproteins,
proteoglycans
collagen
laboratory
indicators
hemostasis.
case,
significant
damage
formation
vicious
circle
observed:
decrease
plasminogen
content,
which
under
action
activators
converted
plasmin,
trigger
factor
fibrinolytic
system,
that
at
same
time
activity
acceleration
dystrophic
processes
accumulation
blood
serum
an
excessive
amount
acute
phase
glycoproteins.
addition,
there
increase
plasma
following
coagulation
markers:
fibrinogen,
soluble
fibrin
monomer
complexes,
D-dimers,
inflammatory
such
as
C-reactive
protein,
haptoglobin.
From
this,
it
follows
postoperative
requires
timely
monitoring
markers,
well
measures
prevent
thrombophilia,
including
prehospital
stage.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: April 14, 2025
Sepsis
is
a
life-threatening
condition
caused
by
dysregulated
host
response
to
infection,
remaining
major
global
health
challenge
despite
clinical
advances.
Therapeutic
challenges
arise
from
antibiotic
misuse,
incomplete
understanding
of
its
complex
pathophysiology,
and
the
unresolved
interplay
immune
dysregulation
microbiota
disruption.
Investigating
microbial
homeostasis
in
shift
cytokine
storm
immunosuppression
may
elucidate
between
metabolites,
dysfunction,
organ
injury,
providing
foundation
for
targeted
therapies
drug
development.
Traditional
Chinese
Medicine
(TCM)
has
demonstrated
significant
advantages
mitigating
sepsis-associated
storms
modulating
gut
homeostasis,
offering
promising
strategy
developing
highly
effective
less
toxic
monomeric
compounds.
Elucidating
interactions
within
immune-inflammation-microbiota
network
sepsis
paves
way
biomarker-driven
personalized
therapeutic
approaches.