Pathogens,
Journal Year:
2024,
Volume and Issue:
14(1), P. 8 - 8
Published: Dec. 27, 2024
Due
to
the
lack
of
agents
that
directly
target
covalently
closed
circular
DNA
and
integrated
HBV
in
hepatocytes,
achieving
a
complete
cure
for
chronic
hepatitis
B
(CHB)
remains
challenging.
The
latest
guidelines
recommend
(hepatitis
surface
antigen)
HBsAg
loss
as
ideal
treatment
improving
liver
function,
histopathology,
long-term
prognosis.
However,
even
after
loss,
virus
can
persist,
with
risk
recurrence,
reactivation,
cirrhosis,
hepatocellular
carcinoma.
Therefore,
follow-up
surveillance
are
still
necessary.
With
increasing
options
available
patients
CHB,
developing
effective
strategies
has
become
crucial.
Recent
studies
on
outcomes
following
provide
new
insights
refining
current
strategies,
though
further
improvement
is
needed
through
observation
follow-up.
PLoS ONE,
Journal Year:
2025,
Volume and Issue:
20(1), P. e0316765 - e0316765
Published: Jan. 13, 2025
Due
to
its
global
burden,
Targeting
Hepatitis
B
virus
(HBV)
infection
in
humans
is
crucial.
Herbal
medicine
has
long
been
significant,
with
flavonoids
demonstrating
promising
results.
Hence,
the
present
study
aimed
establish
a
way
of
identifying
anti-HBV
activities.
Flavonoid
structures
activities
were
retrieved.
A
flavonol-based
pharmacophore
model
was
established
using
LigandScout
v4.4.
Screening
performed
PharmIt
server.
QSAR
equation
developed
and
validated
independent
sets
compounds.
The
applicability
domain
(AD)
defined
Euclidean
distance
calculations
for
validation.
best
model,
consisting
57
features,
generated.
High-throughput
screening
(HTS)
resulted
509
unique
hits.
model's
accuracy
further
set
FDA-approved
chemicals,
sensitivity
71%
specificity
100%.
Additionally,
two
predictors,
x4a
qed,
exhibited
predictive
solid
performance
an
adjusted-R2
value
0.85
0.90
Q2.
PCA
showed
essential
patterns
relationships
within
dataset,
first
components
explaining
nearly
98%
total
variance.
Current
HBV
therapies
tend
fail
provide
complete
cure,
emphasizing
need
new
therapies.
This
study's
importance
highlight
flavonols
as
potential
medicines,
presenting
supplementary
option
existing
therapy.
separate
chemical
sets,
guaranteeing
reproducibility
usefulness
other
by
utilizing
characteristics
X4A
qed.
These
results
possibilities
discovering
future
drugs
integrating
modeling
experimental
research.
Cureus,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 13, 2025
Chronic
hepatitis
B
(CHB)
virus
infection
can
lead
to
severe
liver
diseases,
including
cirrhosis
and
hepatocellular
carcinoma.
The
chronicity
of
the
(HBV)
occurs
because
persistence
viral
covalently
closed
circular
DNA
(cccDNA)
within
hepatocytes.
cccDNA
serves
as
template
for
replication
is
central
HBV,
maintaining
a
reservoir
host.
Despite
therapeutic
advancements,
eliminating
remains
elusive
due
its
evasion
immune
surveillance.
This
review
explores
formation
maintenance
cccDNA,
highlighting
host
factors
influencing
stability
replication.
It
also
discusses
current
treatment
strategies,
interferon-based
therapies
nucleoside/nucleotide
analogs,
which
aim
suppress
Emerging
such
gene
editing
molecular
interventions
hold
promise
targeting
directly.
Currently,
research
focused
on
making
medications
that
target
interest
disrupt
or
clear
reservoir.
However,
future
should
focus
innovative
approaches
directly
minichromosome,
aiming
sustained
suppression
potentially
cure
HBV
infection.
World Journal of Gastroenterology,
Journal Year:
2024,
Volume and Issue:
30(10), P. 1295 - 1312
Published: March 14, 2024
Hepatitis
B
virus
(HBV)
reactivation
is
a
clinically
significant
challenge
in
disease
management.
This
review
explores
the
immunological
mechanisms
underlying
HBV
reactivation,
emphasizing
progression
and
It
delves
into
host
immune
responses
reactivation’s
delicate
balance,
spanning
innate
adaptive
immunity.
Viral
factors’
disruption
of
this
as
are
interactions
between
viral
antigens,
cells,
cytokine
networks,
checkpoint
pathways,
examined.
Notably,
roles
T
natural
killer
antigen-presenting
cells
discussed,
highlighting
their
influence
on
progression.
impact
severity,
hepatic
flares,
liver
fibrosis
progression,
hepatocellular
carcinoma
detailed.
Management
strategies,
including
anti-viral
immunomodulatory
approaches,
critically
analyzed.
The
role
prophylactic
therapy
during
immunosuppressive
treatments
explored
alongside
novel
immunotherapeutic
interventions
to
restore
control
prevent
reactivation.
In
conclusion,
comprehensive
furnishes
holistic
view
that
propel
With
dedicated
focus
understanding
its
implications
for
prospects
efficient
management
article
contributes
significantly
knowledge
base.
more
profound
insights
intricate
elements
system
will
inform
evidence-based
ultimately
enhancing
elevating
patient
outcomes.
dynamic
landscape
strategies
scrutinized,
approaches.
preventing
potential
innovative
proactively
deter
Pharmaceutics,
Journal Year:
2024,
Volume and Issue:
16(2), P. 183 - 183
Published: Jan. 28, 2024
The
success
of
long-acting
(LA)
drug
delivery
systems
(DDSs)
is
linked
to
their
biocompatible
polymers.
These
are
used
for
extended
therapeutic
release.
For
treatment
or
prevention
human
immune
deficiency
virus
type
one
(HIV-1)
infection,
LA
DDSs
hold
promise
improved
regimen
adherence
and
reduced
toxicities.
Current
examples
include
Cabenuva,
Apretude,
Sunlenca.
Each
safe
effective.
Alternative
promising
implants,
prodrugs,
vaginal
rings,
microarray
patches.
can
further
meet
patients’
needs.
We
posit
that
the
physicochemical
properties
formulation
chemical
design
optimize
release
profiles.
strategic
DDS
polymers
will
improve
controlled
simplify
dosing
schedules
adherence.
Pathogens,
Journal Year:
2024,
Volume and Issue:
13(4), P. 291 - 291
Published: March 29, 2024
Infection
with
the
hepatitis
B
virus
(HBV)
is
highly
prevalent
globally.
Over
250
million
people
suffer
from
chronic
B,
and
more
than
800,000
patients
die
each
year
due
to
complications,
including
liver
cancer.
Although
protective
HBV
vaccines
are
recommended
for
all
newborns,
global
coverage
suboptimal.
In
adults,
sexual
transmission
by
far
most
frequent
route
of
contagion.
The
WHO
estimates
that
1.5
new
infections
occur
annually.
Oral
nucleos(t)ide
analogues
entecavir
tenofovir
antivirals
prescribed
as
therapy.
Almost
adherent
medication
achieve
undetectable
plasma
viremia
beyond
6
months
monotherapy.
However,
less
5%
anti-HBs
seroconversion,
viral
rebound
occurs
following
drug
discontinuation.
Therefore,
need
be
lifelong.
New
long-acting
formulations
being
developed
will
maximize
treatment
benefit
overcome
adherence
barriers.
Furthermore,
antiviral
agents
in
development,
entry
inhibitors,
capside
assembly
modulators,
RNA
interference
molecules.
use
combination
therapy
pursues
a
functional
cure,
meaning
it
negative
both
circulating
HBV-DNA
HBsAg.
Even
when
this
goal
achieved,
cccDNA
reservoir
within
infected
hepatocytes
remains
signal
past
infection,
can
reactivate
under
immune
suppression.
gene
therapies,
editing,
eagerly
pursued
silence
or
definitively
disrupt
genomes
and,
way,
ultimately
cure
B.
At
time,
three
actions
taken
push
eradication
globally:
(1)
expand
universal
newborn
vaccination;
(2)
perform
once-in-life
testing
adults
identify
susceptible
persons
could
vaccinated
(or
re-vaccinated)
unveil
asymptomatic
carriers
treatment;
(3)
provide
earlier
carriers,
aviremic
reduces
risk
clinical
progression
transmission.
Virology Journal,
Journal Year:
2025,
Volume and Issue:
22(1)
Published: Feb. 17, 2025
Current
treatments
for
chronic
infection
with
the
hepatitis
B
virus
(HBV)
rarely
cure
carriers
from
disease.
Previously
reported
use
of
serotype
8
adeno-associated
viral
(AAV8)
vectors
to
deliver
expression
cassettes
encoding
anti-HBV
artificial
primary
microRNAs
(apri-miRs)
has
shown
promise
in
preclinical
studies.
A
recently
designed
synthetic
ancestral
AAV
(Anc80L65)
high
liver
transduction
efficiency
is
a
promising
new
addition
vector
toolbox.
This
study
engineered
Anc80L65
express
HBx-targeting
apri-miRs.
Single
dose
administration
cultured
cells
and
HBV
transgenic
mice
effected
reductions
secreted
surface
antigen
(HBsAg).
Circulating
particles
core
(HBcAg)
were
also
significantly
diminished
receiving
apri-miR-expressing
AAVs.
Downregulation
biomarkers
occurred
over
period
12
months.
Absence
inflammatory
responses
or
toxicity
indicated
that
had
good
safety
profile.
These
data
suggest
single
safe
capable
mediating
durable
suppression
gene
expression.
Targeting
HBx,
which
required
transcriptional
activity
covalently
closed
circular
DNA
HBV,
makes
this
Anc80L65-derived
candidate
functional
infection.
Pharmaceuticals,
Journal Year:
2025,
Volume and Issue:
18(3), P. 419 - 419
Published: March 16, 2025
Hepatitis
B
virus
(HBV)
is
an
important
global
public
health
issue.
The
World
Health
Organization
(WHO)
2024
Global
Report
estimated
that
the
prevalence
of
people
living
with
HBV
infection
254
million,
incidence
1.2
million
new
infections
yearly.
Previous
studies
have
shown
natural
compounds
antiviral
inhibition
potentials.
In
silico
methods
such
as
molecular
docking,
virtual
screening,
pharmacophore
modeling,
quantitative
structure–activity
relationship
(QSAR),
and
dynamic
simulations
been
successfully
applied
in
identifying
bioactive
strong
binding
energies
treatment
targets.
COVID-19
pandemic
necessitated
importance
repurposing
already
approved
drugs
using
methods.
This
study
aimed
at
unveiling
benefits
techniques
a
potential
alternative
compounds’
drug
discovery
for
therapy.
Relevant
articles
from
PubMed,
Google
Scholar,
Web
Science
were
retrieved
analyzed.
Furthermore,
this
comprehensively
reviewed
literature
containing
identified
essential
proteins.
Notably,
hesperidin,
quercetin,
kaempferol,
myricetin,
flavonoids
hepatitis
surface
antigen
(HBsAg).
investigation
reveals
offer
understanding
mechanisms
action,
reveal
previously
overlooked
viral
targets
(including
PreS1
Domain
HBsAg
cccDNA
(Covalently
Closed
Circular
DNA)
regulators,
facilitate
creation
specific
inhibitors.
integration
silico,
vitro,
vivo
insights
further
highlight
Moreover,
combination
compounds,
approach,
improves
chances
personalized
precision
medicine
treatment.
Therefore,
we
recommend
strategies
combine
vivo,
approaches
to
effective
drugs.
Long-acting
(LA)
drug-delivery
system
(DDS)
successes
are
linked
to
their
abilities
harness
biocompatible
polymers
and
materials
for
sustained
predictable
release
of
therapeutic
agents
over
an
extended
period
time.
For
human
immune
deficiency
virus
type
one
(HIV-1)
infections,
LA
DDSs
hold
great
promise
in
closing
the
gaps
daily
oral
therapy
treatment
prevention.
Examples
Cabenuva,
Apretude
Sunlenca,
which
have
been
shown
be
safe
effective.
Alternative
promising
drug
delivery
technologies
such
as
implants,
prodrugs,
vaginal
rings,
microarray
patches
being
explored
further
meet
patients’
needs.
We
posit
that
improved
physicochemical
properties
formulation
payloads
material
chemistry
design
with
optimal
kinetics
holds
potential
optimize
profiles.
Furthermore,
prevention
HIV-1
infection,
landscape
medicines
now
clinical
or
preclinical
development
offers
hope
strategic
will
improve
upon
controlled
drugs
simplify
dosing
schedules.