Vaccines,
Journal Year:
2024,
Volume and Issue:
12(1), P. 73 - 73
Published: Jan. 11, 2024
The
intradermal
route
has
emerged
as
a
dose-sparing
alternative
during
the
coronavirus
disease
2019
(COVID-19)
pandemic.
Despite
its
efficacy
in
healthy
populations,
immunogenicity
not
been
tested
immune-mediated
dermatologic
(IMDD)
patients.
This
assessor-blinded,
randomized-controlled,
non-inferiority
trial
recruited
patients
with
two
representative
IMDDs
(i.e.,
psoriasis
and
autoimmune
bullous
diseases)
to
vaccinate
fractionated-dose
(fID)
or
standard
intramuscular
(sIM)
BNT162b2
vaccines
fourth
booster
dose
under
block
randomization
stratified
by
age,
sex,
their
skin
diseases.
Post-vaccination
SARS-CoV-2-specific
IgG
interferon-γ
responses
measured
4
12
weeks
post-intervention
were
serological
surrogates
used
for
demonstrating
treatment
effects.
Mean
differences
log-normalized
outcome
estimates
calculated
multivariable
linear
regression
adjusting
baseline
values,
systemic
immunosuppressants
used,
prior
COVID-19
vaccination
history.
margin
was
set
fID
retain
>80%
of
sIM.
With
109
participants
included,
53
received
(all
entered
an
intention-to-treat
analysis).
demonstrated
sIM
humoral
(mean
sIM:
3.3,
ΔfID-sIM
[mean,
95%CI]:
-0.1,
-0.3
0.0)
cellular
3.2,
0.1,
-0.2
0.3)
outcomes.
Two
from
arm
(3.8%)
developed
injection-site
Koebner's
phenomenon.
Fewer
recipients
experienced
post-vaccination
fever
(fID
vs.
1.9%
12.5%,
Scientific Reports,
Journal Year:
2024,
Volume and Issue:
14(1)
Published: March 27, 2024
Abstract
Brucella
,
a
gram-negative
intracellular
bacterium,
causing
Brucellosis,
zoonotic
disease
with
range
of
clinical
manifestations,
from
asymptomatic
to
fever,
fatigue,
loss
appetite,
joint
and
muscle
pain,
back
severe
patients
have
developed
serious
diseases
affecting
various
organs.
The
mRNA
vaccine
is
an
innovative
type
that
anticipated
supplant
traditional
vaccines.
It
widely
utilized
for
preventing
viral
infections
tumor
immunotherapy.
However,
research
regarding
its
effectiveness
in
bacterial
limited.
In
this
study,
we
analyzed
the
epitopes
two
proteins
brucella
TonB-dependent
outer
membrane
receptor
BtuB
LPS
assembly
protein
LptD,
which
involved
nutrient
transport
synthesis
.
order
effectively
stimulate
cellular
humoral
immunity,
utilize
immunoinformatics
tools
such
as
VaxiJen,
AllergenFPv.1.0
SignalP
5.0
design
proteins.
Finally,
five
cytotoxic
T
lymphocyte
(CTL)
cell
epitopes,
ten
helper
(HTL)
eight
B
were
selected
construct
vaccine.
Computer
simulations
are
also
used
verify
immune
response
codon
optimization,
silico
cloning
showed
can
efficiently
transcript
translate
E.
coli.
secondary
structure
vaccines
tertiary
structures
peptides
predicted
then
docked
TLR-4.
stability
was
confirmed
through
molecular
dynamics
simulation.
These
analyses
multi-epitope
could
potentially
target
extracellular
prevalent
provided
novel
strategies
developing
Vaccines,
Journal Year:
2024,
Volume and Issue:
12(8), P. 873 - 873
Published: Aug. 1, 2024
mRNA
vaccines
are
leading
a
medical
revolution.
technologies
utilize
the
host's
own
cells
as
bio-factories
to
produce
proteins
that
serve
antigens.
This
revolutionary
approach
circumvents
complicated
processes
involved
in
traditional
vaccine
production
and
empowers
with
ability
respond
emerging
or
mutated
infectious
diseases
rapidly.
Additionally,
robust
cellular
immune
response
elicited
by
has
shown
significant
promise
cancer
treatment.
However,
inherent
instability
of
complexity
tumor
immunity
have
limited
its
broader
application.
Although
emergence
pseudouridine
ionizable
cationic
lipid
nanoparticles
(LNPs)
made
clinical
application
possible,
there
remains
substantial
potential
for
further
improvement
immunogenicity
delivered
antigens
preventive
therapeutic
effects
technology.
Here,
we
review
latest
advancements
vaccines,
including
but
not
target
selection
delivery
systems.
offers
multifaceted
perspective
on
this
rapidly
evolving
field.
Signal Transduction and Targeted Therapy,
Journal Year:
2024,
Volume and Issue:
9(1)
Published: Nov. 14, 2024
Abstract
In
the
last
decade,
messenger
ribonucleic
acid
(mRNA)-based
drugs
have
gained
great
interest
in
both
immunotherapy
and
non-immunogenic
applications.
This
surge
can
be
largely
attributed
to
demonstration
of
distinct
advantages
offered
by
various
mRNA
molecules,
alongside
rapid
advancements
nucleic
delivery
systems.
It
is
noteworthy
that
immunogenicity
presents
a
double-edged
sword.
context
immunotherapy,
extra
supplementation
adjuvant
generally
required
for
induction
robust
immune
responses.
Conversely,
non-immunotherapeutic
scenarios,
activation
unwanted
considering
host
tolerability
high
expression
demand
mRNA-encoded
functional
proteins.
Herein,
mainly
focused
on
linear
non-replicating
mRNA,
we
overview
preclinical
clinical
progress
prospects
medicines
encompassing
vaccines
other
therapeutics.
We
also
highlight
importance
focusing
host-specific
variations,
including
age,
gender,
pathological
condition,
concurrent
medication
individual
patient,
maximized
efficacy
safety
upon
administration.
Furthermore,
deliberate
potential
challenges
may
encounter
realm
disease
treatment,
current
endeavors
improvement,
as
well
application
future
advancements.
Overall,
this
review
aims
present
comprehensive
understanding
mRNA-based
therapies
while
illuminating
prospective
development
drugs.
Pathogens and Disease,
Journal Year:
2024,
Volume and Issue:
82
Published: Jan. 1, 2024
Abstract
Chlamydia
trachomatis
is
the
most
prevalent
bacterial
sexually
transmitted
infection
globally.
Antibiotic
treatment
highly
effective,
but
often
asymptomatic
resulting
in
individuals
going
undetected
and
untreated.
This
untreated
can
ascend
to
upper
female
genital
tract
cause
pelvic
inflammatory
disease,
tubal
factor
infertility,
ectopic
pregnancy.
screening
programs
have
failed
control
this
epidemic
demonstrate
need
for
an
efficacious
vaccine
prevent
transmission
disease.
Animal
models
human
epidemiological
data
reveal
that
natural
immunity
provide
partial
or
short-lived
sterilizing
immunity.
These
further
importance
of
eliciting
interferon
gamma
(IFNγ)-producing
cluster
differentiation
4
(CD4)
T
cells
(Th1
Th1/17
cells)
likely
synergize
with
antibody-mediated
opsonophagocytosis
optimal
protection.
studies
guided
preclinical
rational
design
decades
first
Phase
1
clinical
trials
recently
been
completed.
Recent
advances
led
improvements
platforms
clinically
safe
adjuvants
help
a
path
forward.
review
describes
models,
correlates
immunity,
antigen
adjuvant
selection,
future
testing
development.
Pharmaceutical Development and Technology,
Journal Year:
2024,
Volume and Issue:
29(6), P. 559 - 565
Published: May 30, 2024
mRNA-based
vaccines
are
assured
to
significantly
boost
biopharmaceuticals
since
outbreak
of
coronavirus
disease-
2019.
Respiratory
infections,
such
as
influenza,
SARS,
MERS,
COVID-19,
and
respiratory
syncytial
virus,
often
have
high
transmission
rates
due
their
airborne
spread.
infections
can
lead
severe
illness
death.
These
outbreaks
cause
substantial
economic
social
disruption,
seen
with
the
COVID-19
pandemic.
In
our
interconnected
world,
diseases
spread
rapidly
across
borders.
(e.g.,
mRNA-1283)
reduce
by
creating
immunity
in
population,
thus
lowering
incidence
these
diseases.
Vaccines
crucial
for
global
health
security,
helping
prevent
local
from
becoming
pandemics.
Nevertheless,
various
concerns
remain
intracellular
delivery,
susceptibility
degradation
catalytic
hydrolysis,
instability
several
physiological
conditions.
Therefore,
an
hour
needed
address
challenges
opportunities
attaining
high-quality
stable
novel
drug
delivery
systems.
The
authors
contributed
extensive
review
clinical
development,
progress
stability
mitigate
market
needs.
addition,
discuss
advances
growth
date;
which
dominate
scope
therapeutic
implementation.
Finally,
recent
trials,
adjuvant
benefits,
prospects
discussed.
Clinical Microbiology Reviews,
Journal Year:
2024,
Volume and Issue:
37(3)
Published: July 17, 2024
SUMMARY
The
success
of
the
Severe
Acute
Respiratory
Syndrome
Coronavirus
2
mRNA
vaccines
to
lessen/prevent
severe
COVID-19
opened
new
opportunities
develop
RNA
fight
other
infectious
agents.
HIV-1
is
a
lentivirus
that
integrates
into
host
cell
genome
and
persists
for
lifetime
infected
cells.
Multiple
mechanisms
immune
evasion
have
posed
significant
obstacles
development
an
effective
vaccine
over
last
four
decades
since
identification
HIV-1.
Recently,
attempts
address
some
these
challenges
led
multiple
studies
manufactured,
optimized,
tested,
in
different
animal
models,
mRNA-based
vaccines.
Several
clinical
trials
also
been
initiated
or
are
planned
start
soon.
Here,
we
review
current
strategies
applied
vaccines,
discuss
targeting
approaches,
summarize
latest
findings,
offer
insights
future