The Journal of Immunology,
Journal Year:
2024,
Volume and Issue:
213(11), P. 1703 - 1712
Published: Oct. 18, 2024
Abstract
CMV
infection
and
Th17
cells
are
independently
associated
with
increased
risk
for
late
allograft
loss
after
renal
transplantation.
Although
CMV-specific
detectable
in
animal
models
nontransplant
clinical
populations,
evidence
linking
transplantation
remains
unclear.
This
prospective
observational
study
evaluated
a
cohort
of
transplant
recipients
during
12
mo
posttransplant
to
assess
the
presence
peripheral
blood
their
relationship
pretransplant
serostatus
DNAemia.
were
identified
among
donor
(D)+
and/or
recipient
(R)+
expanded
both
primary
(D+/R−)
reactivated
(D+/R+,
D−/R+)
A
subset
coexpressed
IFN-γ,
indicating
Th1/17
phenotype.
These
expressed
CCR6,
CCR5,
activation
terminal
differentiation
markers
(CD95,
OX40,
HLA-DR,
CD57),
central/effector
memory
activating/inhibitory
receptors
(CD57,
4-1BB,
CD160,
CTLA-4,
PD-1)
at
higher
frequencies
than
cells.
In
contrast,
staphylococcal
enterotoxin
B–induced
did
not
expand
DNAemia,
differ
between
groups
over
time,
predominantly
TNF-α,
had
lower
expression
activating
inhibitory
pp65-specific
data
show
that
episodes
DNAemia
recipients,
these
virus-specific
have
distinct
phenotypes
from
global
circulating
Th(1)/17
results
suggest
potential
proinflammatory
pathway
by
which
CMV-induced
may
contribute
injury,
increasing
loss.
Non-coding RNA Research,
Journal Year:
2024,
Volume and Issue:
10, P. 41 - 54
Published: Sept. 2, 2024
In
the
search
for
new
biomarkers
and
therapeutic
targets
infectious
diseases,
several
molecules
have
been
investigated.
Small
RNAs,
known
as
microRNAs
(miRs),
are
important
regulators
of
gene
expression,
emerged
promising
candidates
these
purposes.
MiRs
a
class
small,
endogenous
non-coding
RNAs
that
play
critical
roles
in
human
including
host-pathogen
interaction
mechanisms.
Recently,
miRs
signatures
reported
different
opening
perspectives
molecular
diagnosis
therapy.
MiR
profiles
can
discriminate
between
healthy
individuals
patients,
well
distinguish
disease
stages.
Furthermore,
possibility
assessing
biological
fluids,
such
serum
whole
blood,
renders
feasible
development
non-invasive
diagnostic
prognostic
tools.
this
manuscript,
we
will
comprehensively
describe
diseases
explore
how
they
contribute
to
advance
existing
Additionally,
discuss
miR
analysis
platforms
understand
obstacles
advances
approach
propose
their
potential
clinical
applications
contributions
public
health.
Journal of Interferon & Cytokine Research,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 14, 2025
Coronavirus
disease
2019
(COVID-19)
is
a
deadly
human
viral
with
high
rate
of
infection,
morbidity,
and
mortality.
Although
vaccines
antiviral
treatments
are
available,
hospitalizations
remain
steady,
concerns
about
long-term
consequences
persist.
Therefore,
there
great
urgency
to
develop
novel
therapies.
Here,
we
analyzed
the
role
miR-155,
one
most
powerful
drivers
host
responses
including
immune
inflammatory
responses,
in
pathogenicity
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
infection.
Endogenous
microRNAs
(miRNAs,
miRs)
key
molecules
preventing
entry
replication
while
building
an
cellular
defense.
Our
study
reveals
that
miR-155
expression
elevated
patients
COVID-19.
Using
mouse
model
transgenic
for
angiotensin-converting
enzyme
receptor
2,
evaluated
potential
anti-miR-155
therapy.
Treating
SARS-CoV-2-infected
mice
significantly
reduced
expression,
improved
survival,
slightly
increased
body
weight.
Notably,
these
showed
altered
cytokines
lungs.
These
findings
suggest
could
be
promising
therapy
mitigate
cytokine
storm
long-lasting
symptoms
induced
by
SARS-CoV-2
improving
public
health
outcomes
enhancing
global
pandemic
preparedness.
Frontiers in Immunology,
Journal Year:
2023,
Volume and Issue:
14
Published: Oct. 26, 2023
Autoimmune
diseases
arise
from
atypical
immune
responses
that
attack
self-tissue
epitopes,
and
their
development
is
intricately
connected
to
the
disruption
of
JAK-STAT
signaling
pathway,
where
SOCS
proteins
play
crucial
roles.
Conditions
such
as
autoimmune
uveitis,
psoriasis,
lupus,
encephalitis
exhibit
system
dysfunctions
associated
with
dysregulation.
Emerging
therapeutic
strategies
utilize
inhibitors
mimetics
modulate
alleviate
manifestations.
Although
more
research
clinical
studies
are
required
assess
effectiveness,
safety
profiles,
potential
for
personalized
approaches
in
conditions,
show
promise
treatment
options.
This
review
explores
action,
future
prospects
JAK
agents
systemic
lupus
erythematosus,
encephalitis.
The
findings
underscore
importance
investigating
these
targeted
therapies
advance
options
individuals
suffering
diseases.
Microorganisms,
Journal Year:
2024,
Volume and Issue:
12(5), P. 897 - 897
Published: April 30, 2024
Bovine
coronavirus
(BCoV)
infection
causes
significant
economic
loss
to
the
dairy
and
beef
industries
worldwide.
BCoV
exhibits
dual
tropism,
infecting
respiratory
enteric
tracts
of
cattle.
The
isolates
could
also
induce
manifestations
under
certain
circumstances.
However,
mechanism
this
tropism
has
not
yet
been
studied
well.
MicroRNAs
(miRNAs)
are
small
non-coding
RNAs
that
regulate
gene
expression
play
a
role
in
virus
infection,
mediating
or
modulating
host
immune
regulatory
genes
through
complex
virus–host
cell
interactions.
their
remains
unclear.
This
study
aims
identify
bovine
miRNAs
crucial
for
regulating
interaction,
influencing
tissue
explore
potential
as
biomarkers
therapeutic
agents
against
BCoV.
We
downloaded
18
full-length
genomes
(10
eight
respiratory)
from
GenBank.
applied
several
bioinformatic
tools
targeting
various
regions
viral
genome.
used
criteria
differential
between
enteric/respiratory
some
critical
biological
markers
infection.
Using
online
tools,
we
searched
miRNA
target
involved
evasion,
regulation.
Our
results
show
four
(miR-2375,
miR-193a-3p,
miR-12059,
miR-494)
potentially
spike
protein
at
multiple
sites.
These
suppressor
pathways,
which
negatively
impacts
replication.
Furthermore,
found
bta-(miR-2338,
miR-6535,
miR-2392,
miR-12054)
genome
but
signal
transduction
i.e.,
type
I
interferon
(IFN)
retinoic
acid-inducible
(RIG-I)
pathways.
Moreover,
both
miR-2338
miR-2392
transcriptional
factors
RORA,
YY1,
HLF,
diagnostic
Therefore,
miR-2338,
miR-12054
have
fine-tune
evasion
enhance
pathogenesis.
indicate
essential
roles
pathogenesis,
Four
bta-miR-193a-3p,
bta-miR-12059,
bta-miR-494)
BCoV-S
glycoprotein
suppression
pathways
during
candidates
serve
good
genetic
further
studies
urgently
needed
validate
these
identified
context
markers.
Research Square (Research Square),
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 10, 2025
Abstract
Introduction:
Polymorphonuclear
neutrophils
(PMN)
are
actively
recruited
during
COVID-19
and
yet
dysfunctions
associated
with
its
prognosis.
The
PMN
receptor
CXCR4
ligand
SDF-1/CXCL12
known
to
play
a
role
in
the
recruitment
of
PMN.
primary
objective
was
evaluate
modulation
this
pathway
patients
after
treatment
dexamethasone
(DXM).
Secondary
objectives
were
miRNA
expression
profiles.
Material
Methods
We
conducted
prospective
study
comparing
admitted
emergency
department
from
December
2022
April
2023
for
SARS-CoV-2
infection
control
population.
studied
surface
receptor,
circulating
levels
SDF-1
miR
levels.
Patients
treated
(DXM)
sampled
again
at
H48.
Results
Forty-four
infected
20
controls
analyzed.
significantly
increased
decreased
by
DXM
+
percentages
significantly.
on
admission
risk
mechanical
ventilation.
Levels
15b-5p,
146a-5p,
155-5p
30d-5p
patients.
miR-hsa-122
found
mortality
variation
need
Conclusions
Our
suggests
possible
involvement
SDF-1/CXCR4
axis
physiopathogenesis
COVID-19.
PeerJ,
Journal Year:
2025,
Volume and Issue:
13, P. e18856 - e18856
Published: Jan. 22, 2025
COVID-19
vaccination
is
the
most
effective
strategy
for
preventing
severe
disease
and
death.
Inactivated
vaccines
are
accessible
type
of
in
developing
countries.
Several
studies,
including
work
from
our
group,
have
demonstrated
that
third
dose
(booster
vaccination)
inactivated
vaccine
induces
robust
humoral
cellular
immune
responses.
The
present
study
aimed
to
examine
miRNA
expression
profile
participants
who
received
a
homologous
CoronaVac
vaccine.
Samples
peripheral
blood
mononuclear
cells
(PBMCs)
were
collected
healthcare
volunteers
both
before
1–2
weeks
after
booster
dose.
microarray
analysis
discovery
cohort
six
identified
67
miRNAs
with
differential
expression.
Subsequently,
related
responses
was
examined
validation
31
via
qRT-PCR.
Our
results
validated
miR-25-5p,
miR-34c-3p,
miR-206
post-booster,
significant
correlation
receptor
binding
domain
(RBD)-specific
antibody.
Bioinformatic
suggested
may
target
multiple
pathways
involved
regulation
inflammation.
Therefore,
highlights
PBMCs
as
promising
biomarkers
assessing
response
induced
by
Journal for ImmunoTherapy of Cancer,
Journal Year:
2024,
Volume and Issue:
12(8), P. e009774 - e009774
Published: Aug. 1, 2024
The
importance
of
the
immune
system
in
regulating
tumor
growth
by
inducing
cell-mediated
cytotoxicity
associated
with
patients'
outcomes
has
been
highlighted
past
years
an
increasing
life
expectancy
patients
cancer
on
treatment
different
immunotherapeutics.
However,
tumors
often
escape
surveillance,
which
is
accomplished
mechanisms.
Recent
studies
demonstrated
essential
role
small
non-coding
RNAs,
such
as
microRNAs
(miRNAs),
post-transcriptional
control
modulatory
molecules.
Multiple
methods
have
used
to
identify
miRNAs
targeting
genes
involved
escaping
recognition
including
CTLA-4,
PD-L1,
HLA-G,
components
major
histocompatibility
class
I
antigen
processing
machinery
(APM)
well
other
response-relevant
tumors.
Due
their
function,
these
can
be
(1)
diagnostic
and
prognostic
biomarkers
allowing
discriminate
between
stages
predict
outcome
response
resistance
(immuno)
therapies
(2)
therapeutic
targets
for
patients.
This
review
summarizes
tumor-mediated
escape,
discuss
potential
diagnostic,
predictive
tools
use
therapeutics
alternative
application
methods,
chimeric
receptor
T
cells.