Frontiers in Immunology,
Journal Year:
2022,
Volume and Issue:
13
Published: Aug. 9, 2022
Type
2
helper
T
(Th2)
cells,
a
subset
of
CD4
+
play
an
important
role
in
the
host
defense
against
pathogens
and
allergens
by
producing
Th2
cytokines,
such
as
interleukin-4
(IL-4),
IL-5,
IL-13,
to
trigger
inflammatory
responses.
Emerging
evidence
reveals
that
cells
also
contribute
repair
injured
tissues
after
reactions.
However,
when
tissue
process
becomes
chronic,
excessive,
or
uncontrolled,
pathological
fibrosis
is
induced,
leading
organ
failure
death.
Thus,
proper
control
needed
for
complete
without
induction
fibrosis.
Recently,
existence
pathogenic
(Tpath2)
has
been
revealed.
Tpath2
produce
large
amounts
cytokines
induce
type
inflammation
activated
antigen
exposure
injury.
In
recent
studies,
are
suggested
central
whereas
less
reported
comparison
conventional
cells.
this
review,
we
discuss
roles
sequence
inflammation,
repair,
Signal Transduction and Targeted Therapy,
Journal Year:
2023,
Volume and Issue:
8(1)
Published: June 19, 2023
T
cells
are
crucial
for
immune
functions
to
maintain
health
and
prevent
disease.
cell
development
occurs
in
a
stepwise
process
the
thymus
mainly
generates
CD4
Journal of Stroke,
Journal Year:
2020,
Volume and Issue:
22(1), P. 29 - 46
Published: Jan. 31, 2020
Spontaneous
intracerebral
hemorrhage
(ICH)
is
a
catastrophic
illness
causing
significant
morbidity
and
mortality.
Despite
advances
in
surgical
technique
addressing
primary
brain
injury
caused
by
ICH,
little
progress
has
been
made
treating
the
subsequent
inflammatory
cascade.
Pre-clinical
studies
have
advancements
identifying
components
of
neuroinflammation,
including
microglia,
astrocytes,
T
lymphocytes.
After
cerebral
insult,
inflammation
initially
driven
M1
secreting
cytokines
(e.g.,
interleukin-1β
[IL-1β]
tumor
necrosis
factor-α)
that
are
involved
breakdown
extracellular
matrix,
cellular
integrity,
blood
barrier.
Additionally,
factors
recruit
induce
differentiation
A1
reactive
astrocytes
helper
1
(Th1)
cells,
which
contribute
to
secretion
cytokines,
augmenting
polarization
potentiating
inflammation.
Within
7
days
ICH
ictus,
phenotype
coverts
M2
phenotype,
key
for
hematoma
removal,
tissue
healing,
overall
resolution
The
anti-inflammatory
IL-4,
IL-10)
can
drive
Th2
cell
differentiation.
maintained
additional
suppressing
Th1
phenotypes.
Elucidating
timing
trigger
may
be
integral
improving
clinical
outcomes.
A
challenge
current
translational
research
absence
an
equivalent
disease
animal
model
mirroring
patient
population
comorbid
pathophysiologic
state.
We
review
existing
data
describe
potential
therapeutic
targets
around
we
creating
bench
bedside
better
reflects
pathophysiology
patients.
Journal of Hematology & Oncology,
Journal Year:
2020,
Volume and Issue:
13(1)
Published: Aug. 3, 2020
Abstract
As
crucial
antigen
presenting
cells,
dendritic
cells
(DCs)
play
a
vital
role
in
tumor
immunotherapy.
Taking
into
account
the
many
recent
advances
DC
biology,
we
discuss
how
DCs
(1)
recognize
pathogenic
antigens
with
pattern
recognition
receptors
through
specific
phagocytosis
and
non-specific
micropinocytosis,
(2)
process
small
peptides
proper
sizes
sequences,
(3)
present
MHC-peptides
to
CD4
+
CD8
T
initiate
immune
responses
against
invading
microbes
aberrant
host
cells.
During
anti-tumor
responses,
DC-derived
exosomes
were
discovered
participate
presentation.
cell
microvillar
dynamics
TCR
conformational
changes
demonstrated
upon
Caspase-11-driven
hyperactive
recently
reported
convert
effectors
memory
also
crosstalk
NK
Additionally,
are
most
important
sentinel
for
surveillance
microenvironment.
Alongside
review
latest
developments
DC-based
immunotherapy
preclinical
studies
clinical
trials.
Personalized
vaccine-induced
immunity,
which
targets
tumor-specific
antigens,
has
been
be
promising
form
of
patients
melanoma.
Importantly,
allogeneic-IgG-loaded
HLA-restricted
neoantigen
vaccines
have
robust
effects
mice.
Our
comprehensive
biology
its
aids
understanding
as
mentors
novel
immense
potential.
MedComm,
Journal Year:
2021,
Volume and Issue:
2(4), P. 618 - 653
Published: Dec. 1, 2021
Abstract
Since
nuclear
factor
of
κ‐light
chain
enhancer‐activated
B
cells
(NF‐κB)
was
discovered
in
1986,
extraordinary
efforts
have
been
made
to
understand
the
function
and
regulating
mechanism
NF‐κB
for
35
years,
which
lead
significant
progress.
Meanwhile,
molecular
mechanisms
activation
also
illuminated,
cascades
signaling
events
leading
activity
key
components
pathway
are
identified.
It
has
suggested
plays
an
important
role
human
diseases,
especially
inflammation‐related
diseases.
These
studies
make
attractive
target
disease
treatment.
This
review
aims
summarize
knowledge
family
members
NF‐κB,
as
well
basic
activation.
We
will
effects
dysregulated
on
inflammation,
tumorigenesis,
tumor
microenvironment.
The
progression
translational
study
drug
development
targeting
inflammatory
diseases
cancer
treatment
potential
obstacles
be
discussed.
Further
investigations
precise
functions
physiological
pathological
settings
underlying
urgent
need
develop
drugs
treatment,
with
minimal
side
effects.
Frontiers in Immunology,
Journal Year:
2019,
Volume and Issue:
10
Published: March 6, 2019
Innate
immunity
is
maintained
in
part
by
antigen
presenting
cells
(APCs)
including
dendritic
cells,
macrophages,
and
B
cells.
APCs
interact
with
T
to
link
innate
adaptive
immune
responses.
By
displaying
bacterial
tumorigenic
antigens
on
their
surface
via
major
histocompatibility
complexes,
can
directly
influence
the
differentiation
of
Likewise,
cell
activation,
differentiation,
effector
functions
are
modulated
utilizing
multiple
mechanisms.
The
objective
this
review
describe
how
activation
maintain
during
exposure
microbial
infection
malignant
How
bacteria
cancer
take
advantage
some
these
interactions
for
own
benefit
will
also
be
discussed.
While
cover
a
broad
range
topics,
general
focus
held
around
pathogens,
cancers,
that
typically
occur
within
gastrointestinal
tract.
Annual Review of Immunology,
Journal Year:
2021,
Volume and Issue:
39(1), P. 759 - 790
Published: March 12, 2021
As
the
professional
antigen-presenting
cells
of
immune
system,
dendritic
(DCs)
sense
microenvironment
and
shape
ensuing
adaptive
response.
DCs
can
induce
both
activation
tolerance
according
to
peripheral
cues.
Recent
work
has
established
that
comprise
several
phenotypically
functionally
heterogeneous
subsets
differentially
regulate
T
lymphocyte
differentiation.
This
review
summarizes
mouse
human
DC
subset
phenotypes,
development,
diversification,
function.
We
focus
on
advances
in
our
understanding
how
different
distinct
CD4+
helper
(Th)
cell
differentiation
outcomes,
including
Th1,
Th2,
Th17,
follicular
helper,
regulatory
cells.
intrinsic
properties,
local
tissue
microenvironments,
other
together
determine
Th
during
homeostasis
inflammation.
Frontiers in Immunology,
Journal Year:
2018,
Volume and Issue:
9
Published: June 1, 2018
The
gastrointestinal
tract
is
a
site
of
high
immune
challenge,
as
it
must
maintain
delicate
balance
between
tolerating
luminal
contents
and
generating
an
response
towards
pathogens.
CD4+
T
cells
are
key
in
mediating
the
host
protective
homeostatic
responses.
Yet,
also
known
to
be
main
drivers
inflammatory
bowel
disease
(IBD)
when
this
perturbed.
Many
subsets
have
been
identified
players
perpetuating
chronic
intestinal
inflammation.
Over
last
few
decades,
understanding
how
each
subset
Th
plays
role
has
dramatically
increased.
Simultaneously,
allowed
development
therapeutic
innovation
targeting
specific
molecules
rather
than
broad
immunosuppressive
agents.
Here,
we
review
emerging
evidence
functions
promoting
sustaining
inflammation
that
characterizes
IBD.
Frontiers in Immunology,
Journal Year:
2021,
Volume and Issue:
12
Published: May 3, 2021
Current
success
of
immunotherapy
in
cancer
has
drawn
attention
to
the
subsets
T
H
cells
tumor
which
are
critical
for
activation
anti-tumor
response
either
directly
by
themselves
or
stimulating
cytotoxic
cell
activity.
However,
presence
immunosuppressive
pro-tumorigenic
milieu
further
contributes
complexity
regulation
cell-mediated
immune
response.
In
this
review,
we
present
an
overview
multifaceted
positive
and
negative
effects
cells,
with
emphasis
on
different
subtypes
various
how
a
delicate
balance
contradictory
signals
can
influence
overall
immunotherapy.
We
focus
regulatory
network
that
encompasses
dendritic
cell-induced
CD4
+
1
subsequent
priming
CD8
along
intersecting
anti-inflammatory
2
discuss
other
infiltrating
such
as
immunostimulatory
9
fh
reg
duality
17
function
contribute
tip
anti-
vs
responses
tumor.
highlight
developing
knowledge
against
neoantigens/oncodrivers,
impact
current
strategies
immunity,
opposing
action
be
explored
amplify
patients.
Understanding
nuances
molecular
framework
undergirding
balancing
act
between
is
rational
designing
immunotherapies
bypass
therapeutic
escape
maximize
potential