Headache The Journal of Head and Face Pain,
Journal Year:
2022,
Volume and Issue:
62(8), P. 1046 - 1052
Published: Aug. 25, 2022
Coronavirus
disease
2019
(COVID-19)
vaccine-related
side
effects
are
a
key
concern
with
the
emergence
of
various
types
vaccines
in
market.
We
aimed
to
assess
frequency
and
characteristics
headache
following
different
COVID-19
vaccines.Fully
vaccinated
people
were
recruited
by
convenience
sample
through
an
online
survey
from
September
1
December
1,
2021.
Detailed
analysis
vaccination
was
investigated.
Participants
history
pre-existing
headaches
telephone
interviewed
neurologist
ascertain
type
headache.A
total
1372
participants
participated
(mean
age
32.9
±
11.1).
The
highest
reported
adenoviral
vector
(302/563,
53.6%),
followed
mRNA
(129/269,
48%)
then
inactivated
(188/540,
34.8%).
Recipients
had
significantly
longer
latency
between
onset
(median
8
h
[5:12])
than
recipients
4
[2:8],
p
<
0.001).
Headache
intensity
higher
6
[5:8])
5
[4:7],
Adenoviral
would
increase
likelihood
2.38
times
more
(odds
ratio
[OR]
2.38,
95%
confidence
interval
[CI]
1.83-3.04,
Female
sex
thyroid
associated
related
(OR
1.52,
CI
1.16-1.99;
OR
3.97,
1.55-10.2,
respectively).Recipients
vaccine
should
be
counseled
that
they
may
experience
headaches,
especially
after
type.
However,
such
is
mild
moderate
can
resolve
within
few
days.
Based
on
current
study
design
potential
recall
bias,
these
results
not
generalizable
preliminary.
Signal Transduction and Targeted Therapy,
Journal Year:
2023,
Volume and Issue:
8(1)
Published: April 7, 2023
Abstract
Human
diseases,
particularly
infectious
diseases
and
cancers,
pose
unprecedented
challenges
to
public
health
security
the
global
economy.
The
development
distribution
of
novel
prophylactic
therapeutic
vaccines
are
prioritized
countermeasures
human
disease.
Among
all
vaccine
platforms,
viral
vector
offer
distinguished
advantages
represent
prominent
choices
for
pathogens
that
have
hampered
control
efforts
based
on
conventional
approaches.
Currently,
remain
one
best
strategies
induction
robust
humoral
cellular
immunity
against
diseases.
Numerous
viruses
different
families
origins,
including
vesicular
stomatitis
virus,
rabies
parainfluenza
measles
Newcastle
disease
influenza
adenovirus
poxvirus,
deemed
be
vectors
differ
in
structural
characteristics,
design
strategy,
antigen
presentation
capability,
immunogenicity
protective
efficacy.
This
review
summarized
overall
profile
strategies,
progress
advance
steps
taken
address
barriers
deployment
these
vaccines,
simultaneously
highlighting
their
potential
mucosal
delivery,
application
cancer
as
well
other
key
aspects
concerning
rational
vaccines.
Appropriate
accurate
technological
advances
would
consolidate
position
a
leading
approach
accelerate
breakthroughs
facilitate
rapid
response
emergencies.
Vaccines,
Journal Year:
2022,
Volume and Issue:
10(11), P. 1816 - 1816
Published: Oct. 28, 2022
Zika
virus
(ZIKV),
an
emerging
arthropod-borne
flavivirus,
was
first
isolated
in
Uganda
1947
from
monkeys
and
detected
humans
Nigeria
1952;
it
has
been
associated
with
a
dramatic
burden
worldwide.
Since
then,
interventions
to
reduce
the
of
ZIKV
infection
have
mainly
restricted
mosquito
control,
which
end
proved
be
insufficient
by
itself.
Hence,
situation
prompted
scientists
increase
research
on
antivirals
vaccines
against
virus.
These
efforts
are
still
ongoing
as
pathogenesis
immune
evasion
mechanisms
not
yet
fully
elucidated.
Understanding
viral
disease
mechanism
will
provide
better
landscape
develop
prophylactic
therapeutic
strategies
ZIKV.
Currently,
no
specific
or
drugs
approved
for
However,
some
undergoing
clinical
trials.
Notably,
different
platforms
evaluated
design
vaccines,
including
DNA,
mRNA,
vectors,
virus-like
particles
(VLPs),
inactivated
virus,
live
attenuated
peptide
protein-based
passive
immunizations
using
monoclonal
antibodies
(MAbs),
that
target
vector-derived
antigens.
shown
induce
humoral
cellular
responses
viremia
RNA
titers,
both
vitro
vivo.
This
review
provides
comprehensive
summary
current
advancements
development
Nanoscale,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
Gene
and
RNA-based
therapeutics
represent
a
promising
frontier
in
oncology,
enabling
targeted
modulation
of
tumor-associated
genes
proteins.
This
review
explores
the
latest
advances
payload
vectorization
delivery
systems
developed
for
vivo
cancer
treatments.
We
discuss
viral
non-viral
organic
particles,
including
lipid
based
nanoparticles
polymeric
structures,
effective
transport
plasmids,
siRNA,
self-amplifying
RNA
therapeutics.
Their
physicochemical
properties,
strategies
to
overcome
intracellular
barriers,
innovations
cell-based
carriers
engineered
extracellular
vesicles
are
highlighted.
Moreover,
we
consider
oncolytic
viruses,
novel
capsid
modifications,
approaches
that
refine
tumor
targeting
immunomodulation.
Ongoing
clinical
trials
regulatory
frameworks
guide
future
directions
emphasize
need
safe,
scalable
production.
The
potential
convergence
these
with
combination
therapies
paves
way
toward
personalized
medicine.
Vaccines,
Journal Year:
2023,
Volume and Issue:
11(12), P. 1862 - 1862
Published: Dec. 18, 2023
Hepatitis
B
virus
(HBV)
infection
is
a
global
public
health
problem
that
closely
related
to
liver
cirrhosis
and
hepatocellular
carcinoma
(HCC).
The
prevalence
of
acute
chronic
HBV
infection,
cirrhosis,
HCC
has
significantly
decreased
as
result
the
introduction
universal
vaccination
programs.
first
hepatitis
vaccine
approved
was
developed
by
purifying
surface
antigen
(HBsAg)
from
plasma
asymptomatic
HBsAg
carriers.
Subsequently,
recombinant
DNA
technology
led
development
vaccine.
Although
there
are
already
several
licensed
vaccines
available
for
continuous
research
essential
develop
even
more
effective
vaccines.
Prophylactic
been
important
in
prevention
because
it
effectively
produced
protective
immunity
against
viral
infection.
only
need
provoke
neutralizing
antibodies
directed
envelop
proteins,
whereas
therapeutic
most
likely
needed
induce
comprehensive
T
cell
response
thus,
should
include
other
antigens,
such
core
polymerase.
existing
have
proven
be
highly
preventing
but
ongoing
aims
improve
their
efficacy,
duration
protection,
accessibility.
routine
administration
safe
well-tolerated
worldwide.
purpose
this
type
immunization
trigger
an
immunological
host,
which
will
halt
replication.
clinical
efficacy
safety
affected
number
factors.
However,
success
now
jeopardy
due
breakthrough
infections
caused
variants
with
mutations
S
gene,
high
loads,
virus-induced
immunosuppression.
In
review,
we
describe
various
types
vaccines,
along
recent
progress
battle
new
HBV.
Viruses,
Journal Year:
2023,
Volume and Issue:
15(2), P. 330 - 330
Published: Jan. 24, 2023
Human
adenoviruses
(HAdV)
are
one
of
the
most
important
pathogens
detected
in
acute
respiratory
diseases
pediatrics
and
immunocompromised
patients.
In
1953,
Wallace
Rowe
described
it
for
first
time
oropharyngeal
lymphatic
tissue.
To
date,
more
than
110
types
HAdV
have
been
described,
with
different
cellular
tropisms.
They
can
cause
gastrointestinal
symptoms,
even
urinary
tract
inflammation,
although
infections
asymptomatic.
However,
there
is
a
population
at
risk
that
develop
serious
lethal
conditions.
These
viruses
double-stranded
DNA
genome,
25–48
kbp,
90
nm
diameter,
without
mantle,
stable
environment,
resistant
to
fat-soluble
detergents.
Currently
diagnosis
made
lateral
flow
immunochromatography
or
molecular
biology
through
polymerase
chain
reaction.
This
review
aimed
highlight
variability
pandemic
potential
HAdV3
7
recombinant
could
considering
aggressive
outbreaks
produced
health
facilities.
Herein,
we
characteristics
HAdV,
from
infection
treatment,
vaccine
development,
evaluation
social
determinants
associated
suggesting
necessary
measures
future
sanitary
control
prevent
disasters
such
as
SARS-CoV-2
pandemic,
an
emphasis
on
use
AdV
vaccines
other
pandemics.
Journal of Clinical Investigation,
Journal Year:
2023,
Volume and Issue:
133(12)
Published: May 16, 2023
Dravet
syndrome
(DS),
an
intractable
childhood
epileptic
encephalopathy
with
a
high
fatality
rate,
is
typically
caused
by
loss-of-function
mutations
in
one
allele
of
SCN1A,
which
encodes
NaV1.1,
250-kDa
voltage-gated
sodium
channel.
In
contrast
to
other
epilepsies,
pharmaceutical
treatment
for
DS
limited.
Here,
we
demonstrate
that
viral
vector-mediated
delivery
codon-modified
SCN1A
open
reading
frame
into
the
brain
improves
comorbidities
juvenile
and
adolescent
mice
(Scn1aA1783V/WT).
Notably,
bilateral
vector
injections
hippocampus
and/or
thalamus
increased
survival,
reduced
occurrence
spikes,
provided
protection
from
thermally
induced
seizures,
corrected
background
electrocorticographic
activity
behavioral
deficits,
restored
hippocampal
inhibition.
Together,
our
results
provide
proof
concept
potential
as
therapeutic
approach
infants
adolescents
DS-associated
comorbidities.
Viruses,
Journal Year:
2024,
Volume and Issue:
16(7), P. 1094 - 1094
Published: July 8, 2024
Adenoviruses
are
non-enveloped
DNA
viruses
that
cause
a
wide
range
of
symptoms,
from
mild
infections
to
life-threatening
diseases
in
broad
hosts.
Due
the
unique
characteristics
these
viruses,
they
have
also
become
vehicle
for
gene-transfer
and
cancer
therapeutic
instruments.
Adenovirus
vectors
can
be
used
gene
therapy
by
modifying
wild-type
render
them
replication-defective.
This
makes
it
possible
swap
out
particular
viral
genes
segments
carry
employ
resultant
vector
as
means
delivering
specified
tissues.
In
this
review,
we
outline
progressive
development
adenovirus
vectors,
exploring
their
characteristics,
genetic
modifications,
uses
clinical
preclinical
settings.
A
significant
emphasis
is
placed
on
crucial
role
advancing
therapy,
immunotherapy,
latest
breakthroughs
vaccine
various
diseases.
Journal of Clinical Microbiology,
Journal Year:
2024,
Volume and Issue:
62(9)
Published: Aug. 27, 2024
ABSTRACT
Since
their
discovery
in
1953,
research
on
human
adenoviruses
(HAdVs)
has
had
diverse
foci,
resulted
groundbreaking
discoveries,
such
as
gene
splicing,
and
generated
powerful
oncolytic
constructs
expression
vectors
for
vaccine
development
therapy.
In
contrast,
virologists
working
this
field
have
made
relatively
little
progress
toward
the
prevention
treatment
of
wide
spectrum
HAdV-associated
diseases.
The
understanding
species-specific
features
viral
pathogenesis,
or
mechanisms
underlying
establishment
latency
reactivation,
is
still
limited.
This
group
viruses
currently
comprises
7
species,
51
serotypes,
116
unique
genotypes.
complexity
manifests
with
a
challenging
pathophenotypic
diversity.
Some
types
are
highly
virulent,
others
do
not
seem
to
cause
disease
immunocompetent
hosts.
assessment
load
blood
respiratory
specimens
well-acknowledged
clinical
utility,
but
lack
virus
typing
capabilities
easily
implementable
laboratories
represents
lingering
major
limitation
interpretation
positive
tests.
HAdV
infections
severe
consequences
both
immunocompromised
patients,
why
case
will
require
more
research.
Clinical
isolates
collections
can
provide
resources
investigate
molecular
bases
virulence
fitness
also
help
gather
information
spatial–temporal
patterns
circulation
susceptible
communities,
they
extremely
scarce.
underutilized
interfaces
between
patients
academic
scientists
have,
therefore,
high
potential
become
valuable
collaborators
moving
forward.
Vaccines,
Journal Year:
2025,
Volume and Issue:
13(3), P. 223 - 223
Published: Feb. 24, 2025
Background:
Porcine
epidemic
diarrhea
virus
(PEDV)
is
a
significant
pathogen
in
swine,
causing
substantial
economic
losses
worldwide.
Despite
the
availability
of
existing
vaccines,
there
critical
need
for
novel
vaccine
platforms
that
ensure
robust
protection
while
maintaining
safety.
Methods:
A
recombinant
replication-deficient
vesicular
stomatitis
(VSV)
vaccine,
rVSV∆G-PEDV-S,
was
developed
by
pseudotyping
with
spike
(S)
protein
from
PEDV.
To
achieve
high-titer
pseudotyped
rVSV
particles,
stable
Huh7
cell
line
expressing
PEDV
S
(Huh7-PEDV-S)
generated.
The
infectivity
and
replication
capacity
rVSV∆G-PEDV-S
were
evaluated
PEDV-susceptible
lines
Huh7-PEDV-S
cells.
vaccine’s
immunogenicity
safety
assessed
BALB/c
mice
vaccinated
intramuscularly
rVSV∆G-PEDV-S.
Results:
demonstrated
cells,
remaining
non-complementary
In
mice,
elicited
strong
humoral
immune
response,
characterized
high
levels
S1-specific
IgG
neutralizing
antibodies.
No
adverse
effects,
including
weight
loss
or
behavioral
changes,
observed
confirming
Conclusions:
represents
promising
platform
controlling
outbreaks.
Its
design
methodology
adaptability
to
emerging
variants.
These
findings
highlight
potential
as
safe
effective
solution
ongoing
challenges
posed