Interferons
were
the
original
prototype
cytokine
system
discovered
during
research
of
20th
century.
As
name
suggests
these
originally
considered
to
be
synthesised
and
secreted
between
cells.
However,
technological
advancements
since
dictate
processes
involved
in
secreting
proteins
can
extensively
explained
through
both
genetic
biochemical
pathways
comparatively
clearer.
Interferon
(IFN)
discovery
occurred
when
was
its
infancy.
Simultaneous
by
Franklin
Wilkins
deoxyribonucleic
acid
(DNA)
structure
function
with
Crick
Watson
concurrently;
however,
two
scientists
Isaac
Lindemann
described
first
IFN
1957.
Technological
advancement
allows
comparison,
many
pathogens
mutations
factors
regulation.
Cancer
cell
regulation
has
long
been
central
host
synthesis
and/or
affected
differential
protein
subunits
defined
further
acting
6
domains.
Type
II
remains
immune
as
it
is
released
a
myriad
cells,
mainly
Natural
Killer
T
cells
commonly
used
quantitative
measurement
adaptive
cellular
immunity.
Single–stranded
double–stranded
RNA
DNA
viruses
well
bacterial
infections
(e.g.,
Escherichia)
fungal
Mycobacteria)
affect
systems.
These
utilise
intra/extracellular
like
Toll–like
Receptors
(TLRs)
within
overall
transduction
pathways.
Questions
remain
over
immunological
mechanisms
contributing
innate
type
III
2003
phenotypes
characterised
further.
Changes
I/II/III
IFNs
may
alter
homeostatic
differentially
beneficially
pathological
disorders.
We
therefore
aim
present
rationale
this
regulatory
mechanism
action
context
developments
recently
functional
effects
Frontiers in Microbiology,
Journal Year:
2023,
Volume and Issue:
14
Published: April 28, 2023
The
recognition
of
viral
nucleic
acids
by
host
pattern
receptors
(PRRs)
is
critical
for
initiating
innate
immune
responses
against
infections.
These
are
mediated
the
induction
interferons
(IFNs),
IFN-stimulated
genes
(ISGs)
and
pro-inflammatory
cytokines.
However,
regulatory
mechanisms
to
avoid
excessive
or
long-lasting
that
may
cause
detrimental
hyperinflammation.
Here,
we
identified
a
novel
function
ISG,
IFN
alpha
inducible
protein
27
(IFI27)
in
counteracting
triggered
cytoplasmic
RNA
binding.
Our
model
systems
included
three
unrelated
infections
caused
Influenza
A
virus
(IAV),
Severe
Acute
Respiratory
Syndrome
coronavirus
2
(SARS-CoV-2),
Sendai
(SeV),
transfection
with
an
analog
double-stranded
(ds)
RNA.
Furthermore,
found
IFI27
has
positive
effect
on
IAV
SARS-CoV-2
replication,
most
likely
due
its
ability
counteract
host-induced
antiviral
responses,
including
vivo
.
We
also
show
interacts
PRR
retinoic
acid-inducible
gene
I
(RIG-I),
being
interaction
RIG-I
through
Interestingly,
our
results
indicate
impairs
activation,
providing
molecular
mechanism
modulating
responses.
study
identifies
explain
counterbalancing
preventing
Therefore,
this
will
have
important
implications
drug
design
control
viral-induced
pathology.
Cell & Bioscience,
Journal Year:
2023,
Volume and Issue:
13(1)
Published: Dec. 20, 2023
Type
I
interferon
(IFN-I)
plays
crucial
roles
in
the
regulation
of
inflammation
and
it
is
associated
with
various
inflammatory
diseases
including
systemic
lupus
erythematosus
(SLE),
rheumatoid
arthritis
(RA),
periodontitis,
impacting
people's
health
quality
life.
It
well-established
that
IFN-Is
affect
immune
responses
factors
by
regulating
some
signaling.
However,
currently,
there
no
comprehensive
overview
regulatory
role
IFN-I
distinctive
pathways
as
well
diseases.
This
review
aims
to
provide
a
narrative
involvement
different
signaling
pathways,
mainly
mediating
related
key
specific
targets
cascades
influence
progression
As
such,
we
suggested
induce
through
stimulation
certain
which
displays
possible
efficient
treatment
methods
provides
reference
for
precise
control
Scientific Data,
Journal Year:
2023,
Volume and Issue:
10(1)
Published: July 6, 2023
Abstract
Peripheral
blood
mononuclear
cells
(PBMCs)
are
that
a
critical
part
of
the
immune
system
used
to
fight
off
infection,
defending
our
bodies
from
harmful
pathogens.
In
biomedical
research,
PBMCs
commonly
study
global
response
disease
outbreak
and
progression,
pathogen
infections,
for
vaccine
development
multitude
other
clinical
applications.
Over
past
few
years,
revolution
in
single-cell
RNA
sequencing
(scRNA-seq)
has
enabled
an
unbiased
quantification
gene
expression
thousands
individual
cells,
which
provides
more
efficient
tool
decipher
human
diseases.
this
work,
we
generate
scRNA-seq
data
at
high
depth
(>100,000
reads/cell)
than
30,000
resting,
stimulated,
fresh
frozen
conditions.
The
generated
can
be
benchmarking
batch
correction
integration
methods,
effect
freezing-thawing
cycles
on
quality
cell
populations
their
transcriptomic
profiles.
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(5), P. 2691 - 2691
Published: Feb. 26, 2024
The
role
of
the
IFI6
gene
has
been
described
in
several
cancers,
but
its
involvement
esophageal
cancer
(ESCA)
remains
unclear.
This
study
aimed
to
identify
novel
prognostic
indicators
for
ESCA-targeted
therapy
by
investigating
IFI6's
expression,
epigenetic
mechanisms,
and
signaling
activities.
We
utilized
public
data
from
Gene
Expression
Omnibus
(GEO)
Cancer
Genome
Atlas
(TCGA)
analyze
clinical
characteristics,
function,
pathways,
correlation
with
different
immune
cells
ESCA.
TIMER2.0
database
was
employed
assess
pan-cancer
expression
IFI6,
while
UALCAN
used
examine
across
tumor
stages
histology
subtypes.
Additionally,
KEGG
helped
related
pathways.
Our
findings
revealed
95
genes
positively
correlated
15
negatively
over-expressed
ESCA
other
impacting
patient
survival
showing
higher
tissues
than
normal
tissues.
also
CD4+
T
B
cell
receptors
(BCRs),
both
essential
response.
GO
Biological
Process
(GO
BP)
enrichment
analysis
indicated
that
primarily
associated
Type
I
interferon
pathway
defense
response
viruses.
Intriguingly,
demonstrated
were
mostly
linked
Cytosolic
DNA-sensing
pathway,
which
plays
a
crucial
innate
immunity
viral
defense,
RIG-I-like
receptor
(RLR)
detects
infections
activates
responses.
Pathways
various
identified.
It
is
important
note
our
relied
on
online
databases.
Given
consists
two
distinct
subgroups
(ESCC
EAC),
most
databases
combine
them
into
single
category.
Future
research
should
focus
evaluating
impact
each
subgroup
gain
more
specific
insights.
In
conclusion,
inhibiting
using
targeted
could
be
an
effective
strategy
treating
considering
potential
as
biomarker
factors.
International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(2), P. 579 - 579
Published: Jan. 11, 2025
The
field
of
translational
bioinformatics
is
rapidly
evolving,
driving
the
convergence
molecular
sciences
and
computational
methods
with
their
applications
in
industrial
clinical
practice
[...]
bioRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 14, 2025
Abstract
Inflammation
is
a
complex
host
response
to
harmful
infections
or
injuries,
playing
both
beneficial
and
detrimental
roles
in
tissue
regeneration.
Notably,
clinical
dentinogenesis
associated
with
caries
development
occurs
within
an
inflammatory
environment.
Reparative
closely
linked
intense
inflammation,
which
triggers
the
recruitment
differentiation
of
dental
pulp
stem
cells
(DPSCs)
into
dentin
lineage.
Understanding
how
responses
influence
DPSCs
essential
for
elucidating
mechanisms
underlying
Given
limited
data
on
this
process,
broad
approach
employed
here
gain
deeper
understanding
involved
identify
downstream
signaling
targets.
This
study
aims
investigate
role
inflammation
complement
receptor
C5L2
odontoblastic
transcriptomic
changes
using
poly-A
RNA
sequencing
(RNA-seq).
RNA-seq
techniques
provide
insight
transcriptome
cell,
offering
higher
coverage
greater
resolution
its
dynamic
nature.
Following
stimulation,
exhibit
significantly
altered
gene
profiles,
including
marked
upregulation
key
odontogenic
genes,
highlighting
critical
dentinogenesis.
We
demonstrate
that
TNFα-treated
odontoblast-like
differentiating
DPSCs,
under
modulation,
significant
differential
expression
changes.
The
presented
may
new
avenues
experimental
approaches
uncover
pathways
by
identifying
specific
transcription
factors
profiles.
Journal of Virology,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 25, 2025
ABSTRACT
Long
noncoding
RNAs
(lncRNAs)
are
a
newer
class
of
transcripts
identified
as
key
regulators
biological
processes.
Here,
we
aimed
to
identify
novel
lncRNA
targets
that
play
critical
roles
in
major
human
respiratory
viral
infections
by
systematically
mining
large-scale
transcriptomic
data
sets.
Using
bulk
RNA-sequencing
(RNA-seq)
analysis,
previously
uncharacterized
lncRNA,
named
virus-inducible
modulator
interferon
response
(
VILMIR
),
was
consistently
upregulated
after
vitro
influenza
infection
across
multiple
epithelial
cell
lines
and
A
virus
subtypes.
also
severe
acute
syndrome
coronavirus
2
(SARS-CoV-2)
syncytial
(RSV)
.
We
experimentally
confirmed
the
interferon-beta
(IFN-β)
treatment
A549
line
found
expression
robustly
induced
IFN-β
dose-
time-specific
manner.
Single-cell
RNA-seq
analysis
bronchoalveolar
lavage
fluid
samples
from
disease
2019
(COVID-19)
patients
uncovered
various
types,
including
at
least
five
immune
cells.
The
upregulation
cells
further
T
monocyte
lines,
SUP-T1
THP-1,
treatment.
Finally,
knockdown
reduced
magnitude
host
transcriptional
responses
both
Together,
our
results
show
is
interferon-stimulated
gene
(ISG)
regulates
may
be
potential
therapeutic
target
for
upon
mechanistic
investigation.
IMPORTANCE
Identifying
factors
regulate
developing
new
therapeutics.
Human
long
have
been
regulatory
during
processes;
however,
majority
functions
within
antiviral
remain
unknown.
In
this
study,
influenza,
2,
virus.
demonstrated
an
several
types.
Our
reveal
present
infections.