International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(8), P. 4522 - 4522
Published: April 20, 2024
Here,
we
target
the
high-density
lipoprotein
(HDL)
proteome
in
a
case
series
of
16
patients
with
post-COVID-19
symptoms
treated
HMG-Co-A
reductase
inhibitors
(statin)
plus
angiotensin
II
type
1
receptor
blockers
(ARBs)
for
6
weeks.
Patients
suffering
from
persistent
(post-acute
sequelae)
after
serologically
confirmed
SARS-CoV-2
infection
(post-COVID-19
syndrome,
PCS,
n
=
8)
or
following
vaccination
(PVS,
were
included.
Asymptomatic
subjects
corresponding
serological
findings
served
as
healthy
controls
(n
8/8).
HDL
was
isolated
using
dextran
sulfate
precipitation
and
all
study
participants
analyzed
quantitatively
by
mass
spectrometry.
Clinical
assessed
questionnaires
before
therapy.
The
inflammatory
potential
patients’
addressed
human
endothelial
cells.
PCS
PVS
showed
no
significant
differences;
however,
compared
to
controls,
PVS/PCS
displayed
alterations
involving
hemoglobin,
cytoskeletal
proteins
(MYL6,
TLN1,
PARVB,
TPM4,
FLNA),
amyloid
precursor
protein.
Gene
Ontology
Biological
Process
(GOBP)
enrichment
analysis
identified
hemostasis,
peptidase,
regulation
pathways
be
involved.
Treatment
statins
ARBs
improved
clinical
symptoms.
After
therapy,
three
significantly
increased
(FAM3C,
AT6AP2,
ADAM10;
FDR
<
0.05)
PVS/PCS.
Exposure
cells
revealed
reduced
cytokine
adhesion
molecule
expression.
Thus,
enables
deeper
insight
into
underlying
disease
mechanisms,
pointing
involvement
metabolic
signaling
disturbances.
proteome.
These
observations
may
guide
future
therapeutic
strategies
patients.
Cells,
Journal Year:
2023,
Volume and Issue:
12(6), P. 877 - 877
Published: March 11, 2023
COVID-19
has
a
major
impact
on
cardiovascular
diseases
and
may
lead
to
myocarditis
or
cardiac
failure.
The
clove-like
spike
(S)
protein
of
SARS-CoV-2
facilitates
its
transmission
pathogenesis.
Cardiac
mitochondria
produce
energy
for
key
heart
functions.
We
hypothesized
that
S1
would
directly
impair
the
functions
cardiomyocyte
mitochondria,
thus
causing
dysfunction.
Autoimmunity,
Journal Year:
2023,
Volume and Issue:
56(1)
Published: Sept. 14, 2023
As
a
result
of
the
spread
SARS-CoV-2,
global
pandemic
was
declared.
Indiscriminate
COVID-19
vaccination
has
been
extended
to
include
age
groups
and
naturally
immune
people
with
minimal
danger
suffering
serious
complications
due
COVID-19.
Solid
immuno-histopathological
evidence
demonstrates
that
genetic
vaccines
can
display
wide
distribution
within
body,
affecting
tissues
are
terminally
differentiated
far
away
from
injection
site.
These
heart
brain,
which
may
incur
in
situ
production
spike
protein
eliciting
strong
autoimmunological
inflammatory
response.
Due
fact
every
human
cell
synthesises
non-self
antigens,
inevitably
becomes
target
system,
since
body
is
not
strictly
compartmentalised
accurate
pharmacokinetic
pharmacodynamic
studies
needed
order
determine
precisely
be
harmed.
Therefore,
our
article
aims
draw
attention
scientific
regulatory
communities
critical
need
for
biodistribution
against
COVID-19,
as
well
rational
harm-benefit
assessments
by
group.
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.
npj Vaccines,
Journal Year:
2024,
Volume and Issue:
9(1)
Published: Feb. 15, 2024
Abstract
The
implications
of
administration
mRNA
vaccines
to
individuals
with
chronic
inflammatory
diseases,
including
myocarditis,
rheumatoid
arthritis
(RA),
and
bowel
disease
(IBD),
are
unclear.
We
investigated
vaccine
effects
in
a
inflammation
mouse
model
implanted
an
LPS
pump,
focusing
on
toxicity
immunogenicity.
Under
inflammation,
exacerbated
cardiac
damage
inducing
mild
heart
heightened
pro-inflammatory
cytokine
production
cell
infiltration
the
heart.
Concurrently,
significant
muscle
occurred,
disturbances
mitochondrial
fusion
fission
factors
signaling
impaired
repair.
However,
did
not
adversely
affect
muscles
at
vaccination
site
or
humoral
immune
responses;
nevertheless,
it
partially
reduced
cell-mediated
response,
particularly
T-cell
activation.
These
findings
underscore
importance
addressing
immunogenicity
context
ensuring
their
safe
effective
utilization,
among
vulnerable
populations
immune-mediated
diseases.
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(8), P. 4522 - 4522
Published: April 20, 2024
Here,
we
target
the
high-density
lipoprotein
(HDL)
proteome
in
a
case
series
of
16
patients
with
post-COVID-19
symptoms
treated
HMG-Co-A
reductase
inhibitors
(statin)
plus
angiotensin
II
type
1
receptor
blockers
(ARBs)
for
6
weeks.
Patients
suffering
from
persistent
(post-acute
sequelae)
after
serologically
confirmed
SARS-CoV-2
infection
(post-COVID-19
syndrome,
PCS,
n
=
8)
or
following
vaccination
(PVS,
were
included.
Asymptomatic
subjects
corresponding
serological
findings
served
as
healthy
controls
(n
8/8).
HDL
was
isolated
using
dextran
sulfate
precipitation
and
all
study
participants
analyzed
quantitatively
by
mass
spectrometry.
Clinical
assessed
questionnaires
before
therapy.
The
inflammatory
potential
patients’
addressed
human
endothelial
cells.
PCS
PVS
showed
no
significant
differences;
however,
compared
to
controls,
PVS/PCS
displayed
alterations
involving
hemoglobin,
cytoskeletal
proteins
(MYL6,
TLN1,
PARVB,
TPM4,
FLNA),
amyloid
precursor
protein.
Gene
Ontology
Biological
Process
(GOBP)
enrichment
analysis
identified
hemostasis,
peptidase,
regulation
pathways
be
involved.
Treatment
statins
ARBs
improved
clinical
symptoms.
After
therapy,
three
significantly
increased
(FAM3C,
AT6AP2,
ADAM10;
FDR
<
0.05)
PVS/PCS.
Exposure
cells
revealed
reduced
cytokine
adhesion
molecule
expression.
Thus,
enables
deeper
insight
into
underlying
disease
mechanisms,
pointing
involvement
metabolic
signaling
disturbances.
proteome.
These
observations
may
guide
future
therapeutic
strategies
patients.