Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: Nov. 8, 2024
Due
to
the
vital
importance
of
lungs,
lung-related
diseases
and
their
control
are
very
important.
Severe
inflammatory
responses
mediated
by
immune
cells
were
among
leading
causes
lung
tissue
pathology
damage
during
COVID-19
pandemic.
In
addition,
uncontrolled
cell
can
lead
in
other
infectious
non-infectious
diseases.
It
is
essential
a
way
that
leads
homeostasis.
Immunosuppressive
drugs
only
suppress
do
not
affect
homeostasis
reactions.
The
therapeutic
application
mesenchymal
stem
(MSCs),
addition
restoring
homeostasis,
promote
regeneration
through
production
growth
factors
differentiation
into
cells.
However,
communication
between
MSCs
after
treatment
pulmonary
essential,
investigating
this
help
develop
clinical
perspective.
Different
studies
phase
showed
reverse
fibrosis,
increase
regeneration,
airway
remodeling,
reduce
tissue.
proliferation
potential
one
mechanisms
effects.
Furthermore,
they
secrete
exosomes
function
change
function.
Another
important
mechanism
harmful
with
innate
adaptive
cells,
which
shift
system
toward
regulatory
hemostatic
responses.
Theranostics,
Journal Year:
2024,
Volume and Issue:
14(5), P. 2099 - 2126
Published: Jan. 1, 2024
Exosomes,
which
are
small
vesicles
enclosed
by
a
lipid
bilayer
and
released
many
cell
types,
widely
dispersed
have
garnered
increased
attention
in
the
field
of
regenerative
medicine
due
to
their
ability
serve
as
indicators
diseases
agents
with
therapeutic
potential.
Exosomes
play
crucial
role
mediating
intercellular
communication
through
transfer
biomolecules,
including
proteins,
lipids,
RNA,
other
molecular
constituents,
between
cells.
The
targeted
transport
proteins
nucleic
acids
specific
cells
has
potential
enhance
or
impair
biological
functions.
applications,
they
can
be
used
alone
combination
approaches.
examination
unique
attributes
functions
these
factors
emerged
prominent
study
realm
biomedical
research.
This
manuscript
summarizes
origins
properties
exosomes,
structural,
biological,
physical,
chemical
aspects.
paper
offers
complete
recent
progress
tissue
repair
medicine,
emphasizing
possible
implications
methods
forthcoming
regeneration
attempts.
ACS Omega,
Journal Year:
2023,
Volume and Issue:
8(46), P. 43374 - 43387
Published: Nov. 9, 2023
Exosomes
are
nanoscale
vesicles
secreted
by
living
cells
that
have
similar
membrane
composition
to
parental
and
carry
a
variety
of
proteins,
lipids,
nucleic
acids.
Therefore,
exosomes
certain
biological
activities
play
an
important
role
in
intercellular
communication.
On
the
basis
its
potential
as
carrier
for
drug
delivery
systems,
been
engineered
compensate
shortage
natural
through
various
engineering
strategies
improving
efficiency,
enhancing
targeting
tissues
organs,
extending
circulating
half-life
exosomes.
This
review
focuses
on
loading
drugs
different
strategies,
discussions
exosome
surface
modification
summarizes
advantages
disadvantages
strategies.
In
addition,
this
provides
overview
recent
applications
number
refractory
relapsable
diseases.
has
provide
reference
further
research
development
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(13), P. 7470 - 7470
Published: July 8, 2024
Colorectal
cancer
(CRC)
is
a
significant
public
health
challenge,
with
5-fluorouracil
(5-FU)
resistance
being
major
obstacle
to
effective
treatment.
Despite
advancements,
5-FU
remains
formidable
due
complex
mechanisms
such
as
alterations
in
drug
transport,
evasion
of
apoptosis,
dysregulation
cell
cycle
dynamics,
tumor
microenvironment
(TME)
interactions,
and
extracellular
vesicle
(EV)-mediated
pathways.
Traditional
chemotherapy
often
results
high
toxicity,
highlighting
the
need
for
alternative
approaches
better
efficacy
safety.
Phytochemicals
(PCs)
EVs
offer
promising
CRC
therapeutic
strategies.
PCs,
derived
from
natural
sources,
exhibit
lower
toxicity
can
target
multiple
pathways
involved
progression
resistance.
facilitate
targeted
delivery,
modulate
immune
response,
interact
TME
sensitize
cells
However,
potential
PCs
engineered
overcoming
reshaping
immunosuppressive
underexplored.
Addressing
this
gap
crucial
identifying
innovative
therapies
enhanced
reduced
toxicities.
This
review
explores
multifaceted
evaluates
synergistic
effects
combining
improve
treatment
while
minimizing
adverse
effects.
Additionally,
it
investigates
by
serving
delivery
vehicles
modulating
TME.
By
synthesizing
current
knowledge
addressing
research
gaps,
enhances
academic
understanding
CRC,
interdisciplinary
involving
revolutionizing
therapy.
Further
clinical
validation
are
essential
translating
these
findings
into
improved
patient
outcomes.
Frontiers in Oncology,
Journal Year:
2023,
Volume and Issue:
13
Published: May 23, 2023
Pancreatic
cancer
(PC)
is
one
of
the
most
dangerous
diseases
that
threaten
human
life,
and
investigating
details
affecting
its
progression
or
regression
particularly
important.
Exosomes
are
derivatives
produced
from
different
cells,
including
tumor
cells
other
such
as
Tregs,
M2
macrophages,
MDSCs,
can
help
growth.
These
exosomes
perform
their
actions
by
in
microenvironment,
pancreatic
stellate
(PSCs)
produce
extracellular
matrix
(ECM)
components
immune
responsible
for
killing
cells.
It
has
also
been
shown
cell
(PCC)-derived
at
stages
carry
molecules.
Checking
presence
these
molecules
blood
body
fluids
us
early
stage
diagnosis
monitoring
PC.
However,
system
cell-derived
(IEXs)
mesenchymal
stem
(MSC)-derived
contribute
to
PC
treatment.
Immune
part
mechanisms
involved
surveillance
cell-killing
phenomenon.
be
modified
a
way
antitumor
properties
enhanced.
One
methods
drug
loading
exosomes,
which
significantly
increase
effectiveness
chemotherapy
drugs.
In
general,
form
complex
intercellular
communication
network
plays
role
developing,
progressing,
diagnosing,
monitoring,
treating
cancer.
Research Square (Research Square),
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 6, 2025
Abstract
Background
Type
1
diabetes
(T1D)
is
an
autoimmune
disease,
caused
by
selective
destruction
of
pancreatic
beta
cells,
mediated
mainly
infiltrating
CD8
+
T
cells.
These
cells
also
express
immune
checkpoint
molecules
(ICMs)
which
can
be
targeted
specific
ligands
(ICLs)
as
well
cell-specific
regulatory
(Tregs)
to
induce
immunosuppression.
Methods
We
first
performed
profiling
various
ICMs
on
the
peripheral
in
40
recent-onset
T1D
and
20
age-matched
healthy
subjects
flow
cytometry.
Tregs
were
isolated
from
same
stimulated
with
preproinsulin
(PPI)
in
vitro
generate
PPI-specific
Tregs.
Exosomes
characterized
western
blotting,
transmission
electron
microscopy,
zeta
potential,
particle
size
analysis.
Based
cytometry
data,
we
chose
ICLs
binding
3
most
abundant
(PD-1,
TIGIT,
BTLA)
expressed
for
loading
exosomes.
The
was
optimized
sonication
ICL-loaded
exosomes
(PPI-T-EXOL)
recharacterized.
PPI-T-EXOL
infused
assessed
separately
suppressing
cell
proliferation,
activation
autologous
PPI-pulsed
protection.
Finally,
mice-specific
administered
STZ-induced
diabetic
C57BL/6
mice
inhibit
pathogenesis.
Results
showed
similar
stability
naive
efficiency
incorporation
ICL
PPI-Treg
almost
50%.
inhibited
proliferation
CD4
vitro.
PPI-Tregs
significant
suppression
perforin,
granzyme
B,
IFN-gamma
markers,
C69
CD71
PPI-T-EXOL-infused
protected
(1.1B4
line)
cell-mediated
apoptosis.
Further,
mice,
delayed
onset
hyperglycemia,
particularly
when
before
diabetes.
treatment
partially
controlled
prolonged
survival,
reduced
perivascular
intra-islet
lymphocytic
infiltration,
greater
preservation
Conclusions
Our
results
suggest
that
PPI-Treg-derived
loaded
suppress
responses,
offering
a
promising
therapeutic
intervention
T1D.