International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(10), P. 4559 - 4559
Published: May 9, 2025
Colorectal
cancer
(CRC),
the
third
most
common
worldwide,
is
one
of
deadliest
cancers.
CRC
known
as
a
cold
tumor,
characterized
by
low
immune
response
that
makes
it
difficult
for
cells
to
infiltrate
and
exhibits
strong
resistance
immunotherapy
with
checkpoint
inhibition.
This
restricted
largely
attributed
signature
gene
mutations
including
mismatch
repair
(MMR)
genes,
KRAS,
BRAF,
APC,
TP53,
which
are
also
main
oncogenes
in
CRC.
Mutated
genes
continuously
upregulate
abnormal
signaling
pathways,
leading
excessive
proliferation,
progression,
metastasis.
Furthermore,
reorganizes
tumor
microenvironment
(TME)
recruiting
immunosuppressive
cells.
However,
mutation
can
produce
neoantigens
provoke
an
response,
making
potential
target
immunotherapy.
In
particular,
vaccines
leverage
neoantigenic
properties
these
considered
promising
overcoming
eliciting
anti-tumor
responses.
this
review,
we
will
describe
focus
on
targeting
therapies
BioFactors,
Journal Year:
2022,
Volume and Issue:
49(2), P. 251 - 269
Published: Nov. 3, 2022
Abstract
In
the
last
two
decades,
protein–protein
interactions
(PPIs)
have
been
used
as
main
target
for
drug
development.
However,
with
larger
or
superficial
binding
sites,
it
has
extremely
difficult
to
disrupt
PPIs
small
molecules.
On
other
hand,
intracellular
cannot
be
targeted
by
antibodies
that
penetrate
cell
membrane.
Peptides
a
combination
of
conformational
rigidity
and
flexibility
can
interfaces
appropriate
affinity
specificity.
Since
introduction
insulin
nearly
century
ago,
more
than
80
peptide
drugs
approved
treat
variety
diseases.
These
include
deadly
diseases
such
cancer
human
immunodeficiency
virus
infection.
It
is
also
useful
against
diabetes,
chronic
pain,
osteoporosis.
Today,
research
being
done
on
these
lessons
learned
from
earlier
approaches,
which
are
still
valid
today,
complement
newer
approaches
display
libraries.
At
same
time,
integrated
genomics
libraries
new
strategies
open
avenues
discovery.
The
purpose
this
review
examine
problems
in
elucidating
peptide‐protein
recognition
mechanism.
This
important
develop
peptide‐based
interventions
interfere
endogenous
protein
interactions.
New
developed
improve
specificity
existing
agents
potentially
drugs.
We
highlight
key
challenges
must
overcome
development
realize
their
potential
provide
an
overview
recent
trends
addition,
we
take
in‐depth
look
at
early
efforts
hormone
discovery,
smart
medicinal
chemistry
design,
natural
drugs,
breakthrough
advances
molecular
biology
chemistry.
Virology Journal,
Journal Year:
2024,
Volume and Issue:
21(1)
Published: March 20, 2024
Abstract
Since
1997,
highly
pathogenic
avian
influenza
viruses,
such
as
H5N1,
have
been
recognized
a
possible
pandemic
hazard
to
men
and
the
poultry
business.
The
rapid
rate
of
mutation
H5N1
viruses
makes
whole
process
designing
vaccines
extremely
challenging.
Here,
we
used
an
in
silico
approach
design
multi-epitope
vaccine
against
A
virus
using
hemagglutinin
(HA)
neuraminidase
(NA)
antigens.
B-cell
epitopes,
Cytotoxic
T
lymphocyte
(CTL)
Helper
(HTL)
were
predicted
via
IEDB,
NetMHC-4
NetMHCII-2.3
respectively.
Two
adjuvants
consisting
Human
β-defensin-3
(HβD-3)
along
with
pan
HLA
DR-binding
epitope
(PADRE)
chosen
induce
more
immune
response.
Linkers
including
KK,
AAY,
HEYGAEALERAG,
GPGPGPG
double
EAAAK
utilized
link
epitopes
adjuvants.
This
construct
encodes
protein
having
350
amino
acids
38.46
kDa
molecular
weight.
Antigenicity
~
1,
allergenicity
non-allergen,
toxicity
negative
solubility
appropriate
confirmed
through
Vaxigen,
AllerTOP,
ToxDL
DeepSoluE,
3D
structure
was
refined
validated
Z-Score
−
0.87
overall
Ramachandran
99.7%.
Docking
analysis
showed
could
interact
TLR7
(docking
score
374.08
by
4
hydrogen
bonds)
TLR8
414.39
3
bonds).
Molecular
dynamics
simulations
results
RMSD
RMSF
0.25
nm
0.2
for
H5N1-TLR7
well
0.45
0.4
H5N1-TLR8
complexes,
Mechanics
Poisson-Boltzmann
Surface
Area
(MM/PBSA)
stability
continuity
interaction
between
total
binding
energy
29.97
kJ/mol
23.9
kJ/mol.
Investigating
response
simulation
evidence
ability
stimulate
B
cells
immunity
system
that
shows
merits
this
proposed
candidate
clinical
trials.
Vaccines,
Journal Year:
2025,
Volume and Issue:
13(2), P. 191 - 191
Published: Feb. 15, 2025
Using
plants
as
bioreactors,
molecular
farming
has
emerged
a
versatile
and
sustainable
platform
for
producing
recombinant
vaccines,
therapeutic
proteins,
industrial
enzymes,
nutraceuticals.
This
innovative
approach
leverages
the
unique
advantages
of
plants,
including
scalability,
cost-effectiveness,
reduced
risk
contamination
with
human
pathogens.
Recent
advancements
in
gene
editing,
transient
expression
systems,
nanoparticle-based
delivery
technologies
have
significantly
enhanced
efficiency
versatility
plant-based
systems.
Particularly
vaccine
development,
demonstrated
its
potential
notable
successes
such
Medicago's
Covifenz
COVID-19,
illustrating
capacity
platforms
to
address
global
health
emergencies
rapidly.
Furthermore,
edible
vaccines
opened
new
avenues
mainly
settings
low
resources
where
cold
chain
used
conventional
logistics
is
challenge.
However,
optimization
protein
yield
stability,
complexity
purification
processes,
regulatory
hurdles
are
some
challenges
that
still
remain.
review
discusses
current
status
development
using
operational
mechanisms
plant
platforms,
major
applications
prevention
infectious
diseases,
developments,
nanoparticle-mediated
cancer
vaccines.
The
discussion
will
also
touch
on
ethical
considerations,
framework,
future
trends
respect
transformative
plant-derived
ensuring
greater
accessibility
cost-effectiveness
vaccination.
field
holds
great
promise
disease
area
and,
indeed,
personalized
medicine
biopharmaceuticals
near
future.
Pharmaceutics,
Journal Year:
2023,
Volume and Issue:
15(2), P. 654 - 654
Published: Feb. 15, 2023
The
progress
that
has
been
made
in
computer
science
positioned
silico
studies
as
an
important
and
well-recognized
methodology
the
drug
discovery
development
process.
It
numerous
advantages
terms
of
costs
also
plays
a
huge
impact
on
way
research
is
conducted
since
it
can
limit
use
animal
models
leading
to
more
sustainable
research.
Currently,
human
trials
are
already
being
partly
replaced
by
trials.
EMA
FDA
both
endorsing
these
have
providing
webinars
guidance
support
them.
For
instance,
PBPK
modeling
used
gather
data
interactions
with
other
drugs
clinical
regulatory
requirements
for
pediatric
population,
pregnant
women,
personalized
medicine.
This
trend
evokes
need
understand
role
vaccines,
considering
importance
products
achieved
during
pandemic
their
promising
hope
oncology.
Vaccines
safer
than
current
oncology
treatments.
There
variety
strategies
developing
cancer
vaccine,
some
points
should
be
considered
when
designing
vaccine
technology
following:
delivery
platforms
(peptides,
lipid-based
carriers,
polymers,
dendritic
cells,
viral
vectors,
etc.),
adjuvants
(to
boost
promote
inflammation
at
site,
facilitating
immune
cell
recruitment
activation),
choice
targeted
antigen,
timing
vaccination,
manipulation
tumor
environment,
combination
treatments
might
cause
additive
or
even
synergistic
anti-tumor
effects.
These
many
put
together
outline
best
design.
aim
this
article
perform
review
comprehensive
analysis
design
vaccines
field
infectious
diseases.
authors
intend
literature
all
so
far
preparing
methods
vaccines.
From
point,
was
possible
conclude
there
few
Despite
this,
overview
how
existing
work
could
described.
ACS Omega,
Journal Year:
2024,
Volume and Issue:
unknown
Published: April 2, 2024
Vaccines
are
considered
the
most
effective
tools
for
preventing
diseases.
In
this
sense,
with
Covid-19
pandemic,
effects
of
which
continue
all
over
world,
humanity
has
once
again
remembered
importance
vaccine.
Also,
various
epidemic
outbreaks
that
occurred
previously,
development
processes
vaccines
against
these
viral
pathogens
have
accelerated.
By
efforts,
many
different
new
vaccine
platforms
been
approved
commercial
use
and
introduced
to
landscape.
addition,
innovations
made
in
production
carried
out
conventionally
produced
types
create
a
rapid
response
prevent
potential
epidemics
or
pandemics.
situation,
cell
lines
being
positioned
at
center
generation
as
expression
platforms.
Therefore,
since
main
goal
is
produce
fast,
safe,
disease,
addition
existing
systems,
not
used
until
now
included
first
time.
review,
current
clinical
today
described.
Then,
reason
using
lines,
vaccines,
general
culture-based
mentioned.
selection
parameters
animal
explained
by
considering
bioprocess
efficiency
regulations.
Finally,
their
properties
summarized,
an
emphasis
on
future
status
cultures
industrial
production.
Journal of Controlled Release,
Journal Year:
2024,
Volume and Issue:
378, P. 438 - 459
Published: Dec. 21, 2024
Cancer
vaccines
are
promising
therapeutic
approaches
to
enhance
specific
T-cell
immunity
against
most
solid
tumors.
By
stimulating
anti-tumor
immunity,
clearing
minimal
residual
disease,
and
minimizing
adverse
effects,
these
target
tumor
cells
effective
when
combined
with
immune
checkpoint
blockade
or
other
immunotherapies.
However,
the
development
of
cell-based
faces
quality
issues
due
poor
immunogenicity,
heterogeneity,
a
suppressive
microenvironment,
ineffective
delivery
methods.
In
contrast,
extracellular
vesicles
(EVs),
naturally
released
by
cells,
considered
ideal
drug
carriers
vaccine
platforms.
EVs
offer
highly
organ-specific
targeting,
induce
broader
more
responses,
demonstrate
superior
tissue
ability.
The
EV
is
crucial
for
advancing
cancer
immunotherapy.
Compared
vaccines,
produced
under
Good
Manufacturing
Practices
(GMP)
advantages
such
as
high
safety,
ease
preservation
transport,
wide
range
sources.
This
review
summarizes
latest
research
findings
on
potential
applications
in
this
field.
It
also
highlights
novel
neoantigens
cancer.
Journal of Nanobiotechnology,
Journal Year:
2024,
Volume and Issue:
22(1)
Published: Jan. 3, 2024
Abstract
The
pandemic
caused
by
severe
acute
respiratory
syndrome
coronavirus-2
(SARS-CoV-2)
has
had
a
profound
impact
on
the
global
health
and
economy.
While
mass
vaccination
for
herd
immunity
is
effective,
emerging
SARS-CoV-2
variants
can
evade
spike
protein-based
COVID-19
vaccines.
In
this
study,
we
develop
new
immunization
strategy
utilizing
nanocarrier,
dendritic
mesoporous
silica
nanoparticle
(DMSN),
to
deliver
receptor-binding
domain
(RBD)
conserved
T-cell
epitope
peptides
(DMSN-P-R),
aiming
activate
both
humoral
cellular
immune
responses
in
host.
synthesized
DMSN
good
uniformity
dispersion
showed
strong
ability
load
RBD
peptide
antigens,
enhancing
their
uptake
antigen-presenting
cells
(APCs)
promoting
antigen
delivery
lymph
nodes.
DMSN-P-R
vaccine
elicited
potent
immunity,
characterized
highly
specific
antibodies.
Neutralization
tests
demonstrated
significant
antibody-mediated
neutralizing
activity
against
live
SARS-CoV-2.
Crucially,
also
induced
robust
that
were
specifically
stimulated
of
excellent
biocompatibility
biosafety
vitro
vivo,
along
with
degradability.
Our
study
introduces
promising
utilizes
nanocarriers
range
effectively
prevent
virus
transmission.