Allergy,
Год журнала:
2022,
Номер
77(11), С. 3267 - 3292
Опубликована: Июль 17, 2022
The
inflammation
of
allergic
diseases
is
characterized
by
a
complex
interaction
between
type
2
and
3
immune
responses,
explaining
clinical
symptoms
histopathological
patterns.
Airborne
stimuli
activate
the
mucosal
epithelium
to
release
number
molecules
impacting
activity
resident
environmental
cells.
Signals
from
barrier,
regulatory
cells,
inflamed
tissue
are
crucial
conditions
able
modify
innate
adaptive
effector
cells
providing
selective
homing
eosinophils
or
neutrophils.
high
plasticity
T-
lymphoid
responding
external
signals
prerequisite
explain
multiplicity
endotypes
diseases.
This
notion
paved
way
for
huge
use
specific
biologic
drugs
interfering
with
pathogenic
mechanisms
inflammation.
Based
on
response
epithelial
functions
structural
non-lymphoid
this
review
proposes
some
immunopathogenic
scenarios
characterizing
principal
which
can
be
associated
precise
phenotype
asthma.
Recent
literature
indicates
that
similar
concepts
also
applied
other
non-respiratory
disorders.
next
challenges
will
consist
in
defining
biomarker(s)
each
endotype
allowing
quick
diagnosis
most
effective
personalized
therapy.
Allergy,
Год журнала:
2022,
Номер
77(11), С. 3293 - 3308
Опубликована: Июль 19, 2022
Abstract
Autoimmune
diseases
have
a
prevalence
of
approximately
7
to
9%
and
are
classified
as
either
organ‐specific
diseases,
including
type
I
diabetes,
multiple
sclerosis,
inflammatory
bowel
disease
myasthenia
gravis,
or
systemic
lupus
erythematosus,
rheumatoid
arthritis
Sjögren's
syndrome.
While
many
advancements
been
made
in
understanding
the
mechanisms
autoimmune
disease,
nature
self‐tolerance
its
breakdown,
there
remain
unmet
needs
terms
effective
highly
targeted
treatments.
T
regulatory
cells
(Tregs)
key
mediators
peripheral
tolerance
implicated
result
reduced
numbers
altered
function.
Tregs
may
be
broadly
divided
into
those
generated
thymus
(tTregs)
periphery
(pTregs).
target
different
immune
cell
subsets
tissues
suppress
excessive
inflammation
support
tissue
repair
homeostasis:
is
fine
balance
between
Treg
stability
plasticity
that
required
adjust
Tregs'
purposes
particular
responses.
The
central
role
immunoglobulin
E
(IgE)
allergic
well
recognized,
it
becoming
increasingly
apparent
this
also
has
wider
encompassing
other
disease.
Anti‐IgE
treatment
restores
capacity
plasmacytoid
dendritic
(pDCs)
impaired
by
IgE‐
high‐affinity
IgE
receptor
(FcεR1)
cross‐linking
induce
vitro
atopic
patients.
finding
anti‐IgE
therapy
homeostasis,
mechanism
associated
with
clinical
improvement
asthma
chronic
spontaneous
urticaria
suggests
potential
which
involved.
Allergy,
Год журнала:
2024,
Номер
79(5), С. 1230 - 1241
Опубликована: Фев. 25, 2024
Identifying
predictive
biomarkers
for
allergen
immunotherapy
response
is
crucial
enhancing
clinical
efficacy.
This
study
aims
to
identify
such
in
patients
with
allergic
rhinitis
(AR)
undergoing
subcutaneous
(SCIT)
house
dust
mite
allergy.
EBioMedicine,
Год журнала:
2024,
Номер
103, С. 105098 - 105098
Опубликована: Апрель 11, 2024
BackgroundThe
widespread
involvement
of
tumor-infiltrating
B
cells
highlights
their
potential
role
in
tumor
behavior.
However,
cell
heterogeneity
PDAC
remains
unexplored.
Studying
TIL-Bs
aims
to
identify
new
treatment
strategies.MethodsWe
performed
single-cell
RNA
sequencing
study
the
PDAC.
The
prognostic
and
immunologic
value
identified
CD38+
was
explored
FUSCC
(n
=
147)
TCGA
176)
cohorts.
Flow
cytometry
conducted
characterize
relationship
between
other
immune
cells,
as
well
phenotypic
features.
In
vitro
vivo
experiments
were
assess
putative
effect
on
antitumor
immunity.FindingsThe
presence
associated
with
unfavorable
clinicopathological
features
poorer
overall
survival
(p
<
0.001).
Increased
infiltration
accompanied
by
reduced
natural
killer
(NK)
0.021)
increased
regulatory
T
0.016).
Molecular
profiling
revealed
high
expression
IL-10,
IL-35,
TGF-β,
GZMB,
TIM-1,
CD5
CD21,
confirming
cell-like
Co-culture
demonstrated
suppression
NK
cytotoxicity
cell-derived
IL-10
Finally,
suggested
adoptive
transfer
immunity
administration
a
CD38
inhibitor
hampered
growth
0.001).InterpretationWe
discovered
an
independent
factor
use
may
provide
possibilities
for
immunotherapy.FundingThis
supported
National
Natural
Science
Foundation
China
(U21A20374),
Shanghai
Municipal
Technology
Major
Project
(21JC1401500),
Scientific
Innovation
Education
Committee
(2019-01-07-00-07-E00057),
Special
Clinical
Research
Health
Industry
Commission
(No.
20204Y0265)
(23ZR1479300).
Molecular and Cellular Pediatrics,
Год журнала:
2024,
Номер
11(1)
Опубликована: Янв. 4, 2024
Abstract
Background
As
the
most
common
chronic
disease
in
childhood,
asthma
displays
a
major
public
health
problem
worldwide
with
incidence
of
those
affected
rising.
there
is
currently
no
cure
for
allergic
asthma,
it
mandatory
to
get
better
understanding
underlying
molecular
mechanism.
Main
body
By
producing
IgE
antibodies
upon
allergen
contact,
B
cells
play
pivotal
role
asthma.
Besides
that,
IL-10-secreting
cell
subsets,
namely
regulatory
(Bregs),
are
reported
mice
and
humans
In
humans,
several
Breg
subsets
distinct
phenotypic
functional
properties
identified
among
at
different
maturational
differentiation
stages
that
exert
anti-inflammatory
functions
by
expressing
suppressor
molecules.
Emerging
research
has
focused
on
Bregs
as
well
their
future
diagnostic
preventive
strategies.
Conclusion
Knowledge
about
exact
function
human
still
very
limited.
This
review
aims
summarize
current
knowledge
Bregs.
We
discuss
ways
induction
mechanisms
through
which
they
immunoregulatory
functions,
(childhood)
Multiple
sclerosis
(MS)
is
a
severe
autoimmune
disorder
that
wreaks
havoc
on
the
central
nervous
system,
leading
to
spectrum
of
motor
and
cognitive
impairments.
There
no
cure,
current
treatment
strategies
rely
broad
immunosuppression,
leaving
patients
vulnerable
infections.
To
address
this
problem,
our
approach
aims
induce
antigen-specific
tolerance,
much-needed
shift
in
MS
therapy.
We
have
engineered
tolerogenic
therapy
consisting
spray-dried
particles
made
degradable
biopolymer,
acetalated
dextran,
loaded
with
an
antigenic
peptide
tolerizing
drug,
rapamycin
(Rapa).
After
initial
characterization
optimization,
were
tested
myelin
oligodendrocyte
glycoprotein
(MOG)-induced
experimental
encephalomyelitis
model
MS.
Representing
earliest
possible
time
diagnosis,
mice
treated
at
symptom
onset
early
therapeutic
model,
where
containing
MOG
Rapa+MOG
evoked
significant
reductions
clinical
score.
Particles
then
applied
highly
clinically
relevant
late
during
peak
disease,
each
elicited
dramatic
effect,
reversing
hind
limb
paralysis
restoring
fully
functional
limbs.
confirm
antigen
specificity
therapy,
we
immunized
against
influenza
hemagglutinin
(HA)
them
or
particles.
The
did
not
suppress
antibody
responses
HA.
Our
findings
underscore
potential
particle-based
reverse
autoimmunity
disease-relevant
models
without
compromising
immune
competence,
setting
it
apart
from
existing
treatments.
The Journal of Immunology,
Год журнала:
2022,
Номер
208(2), С. 257 - 266
Опубликована: Янв. 11, 2022
Abstract
This
Brief
Review
delves
into
B
cell
responses
in
the
context
of
allergy.
The
primary
contribution
cells
to
allergy
is
production
IgE,
Ab
isotype
that
triggers
immediate
hypersensitivity
reactions
through
release
mediators
from
mast
and
basophils.
may
also
have
protective
roles
allergy,
such
as
IgG
or
regulatory
cells.
In
this
review,
I
focus
on
basic
principles
differentiation
discuss
features
relevant
allergic
immune
responses.
particular,
discuss:
(1)
class-switch
recombination;
(2)
plasma
differentiation;
(3)
germinal
centers
affinity
maturation;
(4)
memory
recall
responses,
with
an
emphasis
IgG1,
IgG4.
consider
how
contribute
independent
production—for
example,
by
serving
APCs.
Frontiers in Immunology,
Год журнала:
2023,
Номер
14
Опубликована: Окт. 5, 2023
In
the
tumor
milieu
of
head
and
neck
squamous
cell
carcinoma
(HNSCC),
distinct
B
subpopulations
are
present,
which
exert
either
pro-
or
anti-tumor
activities.
Multiple
factors,
including
hypoxia,
cytokines,
interactions
with
cells,
other
immune
infiltrating
lymphocytes
(TILs),
alter
equilibrium
between
dual
roles
cells
leading
to
cancerogenesis.
Certain
subsets
in
microenvironment
(TME)
exhibit
immunosuppressive
function.
These
known
as
regulatory
(Breg)
cells.
Breg
suppress
responses
by
secreting
a
series
IL-10,
IL-35,
TGF-β,
granzyme
B,
adenosine
dampen
effector
TILs
intercellular
contacts.
phenotypes
have
been
discovered
human
mouse
cancer
models.
However,
when
compartmentalized
within
tertiary
lymphoid
structure
(TLS),
predominantly
play
effects.
A
mature
TLS
contains
CD20
+
zone
several
important
types
germinal-center
like
antibody-secreting
plasma
memory
They
kill
via
antibody-dependent
cytotoxicity
phagocytosis,
local
complement
activation
TLSs
also
privileged
sites
for
T
coordination
activation.
Nonetheless,
some
cases,
may
serve
niche
hidden
indicate
bad
prognosis.
Thus,
TIL-B
bidirectional
immune-modulatory
activity
responsive
variety
immunotherapies.
this
review,
we
discuss
functional
distinctions
immunogenic
that
focus
on
tumors
HNSCC
patients.
Additionally,
review
contemporary
immunotherapies
aim
target
For
development
innovative
therapeutic
approaches
T-cell-based
immunotherapy,
full
understanding
is
necessary.