MedComm,
Journal Year:
2023,
Volume and Issue:
4(3)
Published: June 1, 2023
Gene
therapy,
a
medical
approach
that
involves
the
correction
or
replacement
of
defective
and
abnormal
genes,
plays
an
essential
role
in
treatment
complex
refractory
diseases,
such
as
hereditary
cancer,
rheumatic
immune
diseases.
Nucleic
acids
alone
do
not
easily
enter
target
cells
due
to
their
easy
degradation
vivo
structure
cell
membranes.
The
introduction
genes
into
biological
is
often
dependent
on
gene
delivery
vectors,
adenoviral
which
are
commonly
used
therapy.
However,
traditional
viral
vectors
have
strong
immunogenicity
while
also
presenting
potential
infection
risk.
Recently,
biomaterials
attracted
attention
for
use
efficient
vehicles,
because
they
can
avoid
drawbacks
associated
with
vectors.
Biomaterials
improve
stability
nucleic
efficiency
intracellular
delivery.
This
review
focused
biomaterial-based
systems
therapy
disease
treatment.
Herein,
we
recent
developments
modalities
Additionally,
discuss
acid
strategies,
focus
systems.
Furthermore,
current
applications
summarized.
Exploration,
Journal Year:
2023,
Volume and Issue:
4(2)
Published: Nov. 17, 2023
Abstract
mRNA
therapeutics
have
emerged
as
powerful
tools
for
cancer
immunotherapy
in
accordance
with
their
superiority
expressing
all
sequence‐known
proteins
vivo.
In
particular,
a
small
dosage
of
delivered
mRNA,
antigen‐presenting
cells
(APCs)
can
synthesize
mutant
neo‐antigens
and
multi‐antigens
present
epitopes
to
T
lymphocytes
elicit
antitumor
effects.
addition,
receptors
like
chimeric
antigen
receptor
(CAR),
T‐cell
(TCR),
CD134,
immune‐modulating
factors
including
cytokines,
interferons,
antibodies
specific
enhance
immunological
response
against
tumors.
With
the
maturation
vitro
transcription
(IVT)
technology,
large‐scale
pure
encoding
be
synthesized
quickly.
However,
clinical
translation
mRNA‐based
anticancer
strategies
is
restricted
by
delivering
into
target
organs
or
inadequate
endosomal
escape
efficiency
mRNA.
Recently,
there
been
some
advances
immunotherapy,
which
roughly
classified
modifications
structure
development
delivery
systems,
especially
lipid
nanoparticle
platforms.
this
review,
latest
overcoming
limitations
immunotherapies
recent
are
summarized.
Challenges
opportunities
applications
also
discussed.
Pharmaceutics,
Journal Year:
2023,
Volume and Issue:
15(4), P. 1127 - 1127
Published: April 3, 2023
In
recent
years,
there
has
been
an
increase
in
deaths
due
to
infectious
diseases,
most
notably
the
context
of
viral
respiratory
pathogens.
Consequently,
focus
shifted
search
for
new
therapies,
with
attention
being
drawn
use
nanoparticles
mRNA
vaccines
targeted
delivery
improve
efficacy
these
vaccines.
Notably,
vaccine
technologies
denote
as
a
era
vaccination
their
rapid,
potentially
inexpensive,
and
scalable
development.
Although
they
do
not
pose
risk
integration
into
genome
are
produced
from
elements,
challenges,
including
exposing
naked
mRNAs
extracellular
endonucleases.
Therefore,
development
nanotechnology,
we
can
further
efficacy.
Nanoparticles,
nanometer
dimensions,
move
more
freely
body
and,
small
size,
have
unique
physical
chemical
properties.
The
best
candidates
transfer
lipid
(LNPs),
which
stable
biocompatible
contain
four
components:
cationic
lipids,
ionizable
polyethylene
glycols
(PEGs),
cholesterol,
used
facilitate
cytoplasmic
delivery.
this
article,
components
system
mRNA-LNP
against
lung
infections
such
influenza,
coronavirus,
syncytial
virus
reviewed.
Moreover,
provide
succinct
overview
current
challenges
potential
future
directions
field.
Theranostics,
Journal Year:
2024,
Volume and Issue:
14(2), P. 738 - 760
Published: Jan. 1, 2024
The
mRNA
vaccine,
a
groundbreaking
advancement
in
the
field
of
immunology,
has
garnered
international
recognition
by
being
awarded
prestigious
Nobel
Prize,
which
emerged
as
promising
prophylactic
and
therapeutic
modality
for
various
diseases,
especially
cancer,
rare
disease,
infectious
disease
such
COVID-19,
wherein
successful
treatment
can
be
achieved
improving
stability
introducing
safe
effective
delivery
system.
Nanotechnology-based
systems,
lipid
nanoparticles,
lipoplexes,
polyplexes,
lipid-polymer
hybrid
nanoparticles
others,
have
attracted
great
interest
been
explored
delivery.
Nanoscale
platforms
protect
from
extracellular
degradation
while
promoting
endosome
escape
after
endocytosis,
hence
efficacy.
This
review
provides
an
overview
diverse
nanoplatforms
utilized
preclinical
clinical
stages,
including
formulation,
preparation
process,
transfection
efficiency,
administration
route.
Furthermore,
market
situation
prospects
vaccines
are
discussed
here.
Journal of Nanobiotechnology,
Journal Year:
2024,
Volume and Issue:
22(1)
Published: July 4, 2024
Abstract
Messenger
RNA
(mRNA)
has
emerged
as
a
promising
therapeutic
molecule
with
numerous
clinical
applications
in
treating
central
nervous
system
disorders,
tumors,
COVID-19,
and
other
diseases.
mRNA
therapies
must
be
encapsulated
into
safe,
stable,
effective
delivery
vehicles
to
preserve
the
cargo
from
degradation
prevent
immunogenicity.
Exosomes
have
gained
growing
attention
because
of
their
good
biocompatibility,
low
immunogenicity,
small
size,
unique
capacity
traverse
physiological
barriers,
cell-specific
tropism.
Moreover,
these
exosomes
can
engineered
utilize
natural
carriers
target
specific
cells
or
tissues.
This
targeted
approach
will
enhance
efficacy
reduce
side
effects
mRNAs.
However,
difficulties
such
lack
consistent
reliable
methods
for
exosome
purification
efficient
encapsulation
large
mRNAs
addressed.
article
outlines
current
breakthroughs
cell-derived
vesicle-mediated
its
biomedical
applications.
Graphical
Frontiers in Bioengineering and Biotechnology,
Journal Year:
2025,
Volume and Issue:
13
Published: March 12, 2025
The
advent
of
mRNA
vaccines,
accelerated
by
the
global
response
to
COVID-19
pandemic,
marks
a
transformative
shift
in
vaccine
technology.
In
this
article,
we
discuss
development,
current
applications,
and
prospects
vaccines
for
both
prevention
treatment
infectious
diseases
oncology.
By
leveraging
capacity
encode
antigens
within
host
cells
directly,
provide
versatile
scalable
platform
suitable
addressing
broad
spectrum
pathogens
tumor-specific
antigens.
We
highlight
recent
advancements
design,
innovative
delivery
mechanisms,
ongoing
clinical
trials,
with
particular
emphasis
on
their
efficacy
combating
diseases,
such
as
COVID-19,
Zika,
influenza,
well
emerging
potential
cancer
immunotherapy.
also
address
critical
challenges,
including
stability,
optimization
immune
responses,
broader
issue
accessibility.
Finally,
review
strategies
advancing
next-generation
aim
overcoming
limitations
technology
enhancing
preventive
therapeutic
approaches
oncological
diseases.
Journal of Controlled Release,
Journal Year:
2021,
Volume and Issue:
338, P. 201 - 210
Published: Aug. 18, 2021
Self-amplifying
RNA
(saRNA)
is
a
next-generation
vaccine
platform,
but
like
all
nucleic
acids,
requires
delivery
vehicle
to
promote
cellular
uptake
and
protect
the
saRNA
from
degradation.
To
date,
platforms
for
have
included
lipid
nanoparticles
(LNP),
polyplexes
cationic
nanoemulsions;
of
these
LNP
are
most
clinically
advanced
with
recent
FDA
approval
COVID-19
based-modified
mRNA
vaccines.
While
effect
on
immunogenicity
well
studied,
role
biomaterials
in
effectiveness
under
investigated.
Here,
we
tested
formulated
either
pABOL,
bioreducible
polymer,
or
LNP,
characterized
protein
expression
both
platforms.
We
observed
that
pABOL-formulated
resulted
higher
magnitude
expression,
formulations
were
overall
more
immunogenic.
Furthermore,
helper
phospholipid
route
administration
(intramuscular
versus
intranasal)
impacted
two
model
antigens
(influenza
hemagglutinin
SARS-CoV-2
spike
protein).
administered
intramuscularly,
not
pABOL
intranasally,
increased
acute
interleukin-6
after
vaccination.
Overall,
results
indicate
systems
routes
may
fulfill
different
niches
within
field
genetic
medicines.
ACS Nano,
Journal Year:
2021,
Volume and Issue:
15(11), P. 17582 - 17601
Published: Oct. 27, 2021
The
COVID-19
pandemic
is
caused
by
the
coronavirus
SARS-CoV-2
(SC2).
A
variety
of
anti-SC2
vaccines
have
been
approved
for
human
applications,
including
those
using
messenger
RNA
(mRNA),
adenoviruses
expressing
SC2
spike
(S)
protein,
and
inactivated
virus.
protective
periods
immunization
afforded
these
intramuscularly
administered
are
currently
unknown.
An
alternative
self-administrable
vaccine
capable
mounting
long-lasting
immunity
via
sterilizing
neutralizing
antibodies
would
be
hugely
advantageous
in
tackling
emerging
mutant
variants.
This
could
also
diminish
possibility
vaccinated
individuals
acting
as
passive
carriers
COVID-19.
Here,
we
investigate
potential
an
intranasal
(IN)-delivered
DNA
encoding
S
protein
BALB/c
C57BL/6J
immunocompetent
mouse
models.
immune
response
to
IN
delivery
this
SC2-spike
transported
on
a
modified
gold-chitosan
nanocarrier
shows
strong
consistent
surge
(IgG,
IgA,
IgM)
effective
neutralization
pseudoviruses
proteins
different
variants
(Wuhan,
beta,
D614G).
Immunophenotyping
histological
analyses
reveal
chronological
events
involved
recognition
antigen
resident
dendritic
cells
alveolar
macrophages,
which
prime
draining
lymph
nodes
spleen
peak
SC2-specific
cellular
humoral
responses.
attainable
high
levels
IgA
lung
mucosa
tissue-resident
memory
T
can
efficiently
inhibit
its
at
site
entry
provide
immunity.
Journal of Tissue Engineering,
Journal Year:
2022,
Volume and Issue:
13
Published: Jan. 1, 2022
In
the
past
decade,
microneedle-based
drug
delivery
systems
showed
promising
approaches
to
become
suitable
and
alternative
for
hypodermic
injections
can
control
agent
without
side
effects
compared
conventional
approaches.
Despite
these
advantages,
procedure
of
microfabrication
is
facing
some
difficulties.
For
instance,
loading
method,
stability
drugs,
retention
time
are
subjects
debate.
Besides,
application
novel
refining
fabrication
methods,
types
materials,
instruments
other
issues
that
need
further
attention.
Herein,
we
tried
summarize
recent
achievements
in
controllable
(microneedle
patches)
vitro
vivo
settings.
addition,
discussed
influence
delivered
drugs
on
cellular
mechanism
immunization
molecular
signaling
pathways
through
intradermal
route.
Understanding
putative
efficiency
microneedle
patches
human
medicine
help
us
develop
design
sophisticated
therapeutic
modalities.
ACS Nano,
Journal Year:
2022,
Volume and Issue:
16(11), P. 18936 - 18950
Published: Oct. 21, 2022
Ionizable
cationic
lipid-containing
lipid
nanoparticles
(LNPs)
are
the
most
clinically
advanced
non-viral
gene
delivery
platforms,
holding
great
potential
for
therapeutics.
This
is
exemplified
by
two
COVID-19
vaccines
employing
mRNA-LNP
technology
from
Pfizer/BioNTech
and
Moderna.
Herein,
we
develop
a
chemical
library
of
ionizable
lipids
through
one-step
chemical-biological
enzyme-catalyzed
esterification
method,
synthesized
were
further
prepared
to
be
LNPs
mRNA
delivery.
Through
orthogonal
design
experiment
methodology
screening,
top-performing
AA3-DLin
show
outstanding
efficacy
long-term
storage
capability.
Furthermore,
LNP
encapsulating
SARS-CoV-2
spike
mRNAs
successfully
induced
strong
immunogenicity
in
BALB/c
mouse
model
demonstrated
antibody
titers,
virus
challenge,
T
cell
immune
response
studies.
The
developed
an
excellent
platform,
this
study
provides
overall
perspective
lipids,
aspects
design,
synthesis,
optimization,
fabrication,
characterization,
application.