Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: May 15, 2025
Background
Atopic
dermatitis
(AD),
a
prevalent
inflammatory
skin
disease
affecting
10%-20%
of
the
population,
is
linked
to
development
asthma
through
atopic
march
(AM).
This
study
aims
explore
role
basophils
in
OVA-induced
lung
inflammation
presence
AD-like
lesions
and
investigate
potential
contribution
thymic
stromal
lymphopoietin
(TSLP)
activating
basophils.
Methods
Mouse
AM
models
were
established
C57BL/6
mice
using
MC903
OVA
epicutaneous
sensitization,
followed
by
intranasal
challenges.
An
intraperitoneal
OVA-sensitized
model
was
employed
as
control
group.
RNA-Seq
analysis
conducted
on
CD45
+
immune
cells
from
these
models.
Histologic
examinations,
flow
cytometry,
ELISA
used
examine
systemic
response.
Basophil
depletion
achieved
administration
anti-FcϵRIα
mAb.
The
TSLP
investigated
TSLPR
knockout
mice.
Results
As
sensitization
model,
also
induced
eosinophilic
mice,
resembling
process.
revealed
differential
gene
expression,
with
genes
related
being
prominent
model.
Increased
basophil
activation
IL-4
production
observed
epicutaneously
sensitized
attenuated
inflammation.
levels
increased
topical
MC903,
reduced
inflammation,
suggesting
involved
activation.
Conclusion
Basophils
play
crucial
context
lesions,
appears
drive
Understanding
interactions
provides
insights
for
therapeutic
interventions
AM-associated
conditions.
Pediatric Drugs,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 22, 2025
Pediatric
asthma
remains
a
prevalent
and
challenging
chronic
condition
globally,
affecting
quality
of
life
imposing
significant
burdens
on
families
healthcare
systems.
Despite
advancements
in
understanding
pathophysiology
treatment,
key
controversies
persist
optimizing
management
strategies.
Inhaled
corticosteroids
(ICS)
are
the
cornerstone
reducing
inflammation
preventing
exacerbations.
While
concerns
about
growth
suppression
exist,
evidence
suggests
that
this
effect
is
primarily
associated
with
high
doses
prolonged
use,
rather
than
standard
maintenance
therapy.
Nonetheless,
adherence
to
ICS
suboptimal,
necessitating
strategies
ensure
effective
sustained
treatment.
The
introduction
reliever
therapy
(MART)
ICS–formoterol
has
offered
improved
outcomes
by
simplifying
regimens
reliance
short-acting
beta-agonists
(SABA).
However,
supporting
MART
ICS-SABA
younger
children
limited,
highlighting
gaps
pediatric-focused
research.
Biologics
targeting
inflammatory
pathways,
such
as
omalizumab,
mepolizumab,
dupilumab,
represent
personalized
approach
for
severe
but
face
challenges
including
costs,
limited
long-term
safety
data,
uncertainty
regarding
their
ability
modify
disease
progression.
In
addition,
complexity
treatment
decisions
compounded
insufficient
biomarkers
age-specific
guide
Addressing
these
requires
robust
clinical
studies
tailored
pediatric
populations.
This
review
critically
examines
current
pharmacological
strategies,
unresolved
issues,
evolving
approaches
management,
emphasizing
need
evidence-based
care.
Enhancing
necessitates
balancing
therapeutic
benefits
minimal
adverse
effects
leveraging
ongoing
research
inform
future
practice.
Allergies,
Journal Year:
2025,
Volume and Issue:
5(2), P. 9 - 9
Published: March 27, 2025
Background:
Atopic
dermatitis
(AD),
allergic
rhinitis
(AR),
and
chronic
rhinosinusitis
with
nasal
polyps
(CRSwNP)
represent
interconnected
conditions
within
the
spectrum
of
type
2
inflammatory
diseases.
While
these
share
common
genetic
epigenetic
pathways,
precise
molecular
mechanisms
remain
underexplored.
Methods:
This
review
integrates
latest
insights
on
factors
linking
AD,
AR,
CRSwNP,
focusing
genome-wide
association
studies,
DNA
methylation
patterns,
histone
modifications,
microRNA
regulation.
Results:
In
all
three
conditions,
including
(Me)
acetylation
(Ac)
methylation,
regulate
barrier-related
genes,
influencing
disease
severity.
Notably,
miRNAs
such
as
miR-146a
miR-155
play
pivotal
roles
in
modulating
inflammation
across
diseases,
while
disease-specific
contribute
to
airway
remodeling
(miR-125b
miR-21
AR
CRSwNP).
Emerging
evidence
underscores
role
microbiome-driven
inflammasome
activation
matrix
metalloproteinases
(MMP-2,
MMP-9,
MMP-12)
perpetuating
remodeling.
Conclusions:
The
interplay
between
predispositions,
exposomal
systemic
nature
inflammation.
A
deeper
understanding
could
lead
transformative,
personalized
diagnostic
therapeutic
advancements.
Immunological Reviews,
Journal Year:
2025,
Volume and Issue:
331(1)
Published: March 31, 2025
Type
2-mediated
immune
responses
protect
the
body
against
environmental
threats
at
barrier
surfaces,
such
as
large
parasites
and
toxins,
facilitate
repair
of
inflammatory
tissue
damage.
However,
maladaptive
to
typically
nonpathogenic
substances,
commonly
known
allergens,
can
lead
development
allergic
diseases.
2
immunity
involves
a
series
prototype
TH2
cytokines
(IL-4,
IL-5,
IL-13)
alarmins
(IL-33,
TSLP)
that
promote
generation
adaptive
CD4+
helper
cells
humoral
products
allergen-specific
IgE.
Mast
basophils
are
integral
players
in
this
network,
serving
primary
effectors
IgE-mediated
responses.
These
bind
IgE
via
high-affinity
receptors
(FcεRI)
expressed
on
their
surface
and,
upon
activation
by
release
variety
mediators
regulate
responses,
attract
modulate
other
cells,
contribute
repair.
Here,
we
review
biology
effector
mechanisms
these
focusing
primarily
role
mediating
both
physiological
pathological
contexts.
Vaccines,
Journal Year:
2025,
Volume and Issue:
13(5), P. 448 - 448
Published: April 24, 2025
Background:
Food
allergy
(FA)
poses
a
major
global
health
issue
due
to
the
increasing
prevalence
and
lack
of
effective
prevention
strategies.
Allergen-specific
immunotherapy
(AIT)
has
emerged
as
disease-modifying
therapy
for
FA.
However,
long-term
treatment
duration
unexpected
adverse
reactions,
only
minority
patients
benefit
from
AIT.
Therefore,
prophylactic
interventions
are
urgently
needed
FA
patients.
Methods:
In
this
proof-of-concept
study,
using
well-established
mRNA
platform,
we
developed
vaccine
candidates
encoding
egg
white
allergen
Gal
d2
comprehensively
evaluated
their
efficacy
against
anaphylaxis
in
d2-induced
allergic
mouse
model.
Results:
Two
formulations,
d2-IL-10
vaccine,
both
demonstrated
potent
ability
inducing
allergen-specific
IgG
Th1-type
T
cells.
Importantly,
two
formulations
showed
promise
preventing
onset
disease,
which
is
indicated
by
body
temperature
decline
during
anaphylaxis.
Conclusions:
We
provided
preliminary
evidence
showing
that
platform
unique
holds
development
anti-allergy
vaccines.
This
largely
attributed
capacities
vaccines
eliciting
an
allergen-blocking
antibody,
shifting
Th2
towards
Th1
immunity,
well
generating
peripheral
tolerance.
further
investigations
required
better
understand
mode
action.
Frontiers in Allergy,
Journal Year:
2025,
Volume and Issue:
6
Published: April 30, 2025
Allergic
disorders
encompass
a
variety
of
conditions
including
asthma,
atopic
dermatitis,
food
allergy,
allergic
rhinitis,
and
eosinophilic
esophagitis.
These
are
connected
via
an
abnormal
host
immune
response
to
the
environment.
A
series
longitudinal
cross-sectional
studies
conducted
over
past
3
decades
have
reported
on
epidemiological
trends
that
contribute
towards
development
pediatric
asthma
disease.
Infant
birth
cohort
assessing
microbiome
offered
clues
as
underlying
biological
mechanisms
basis
for
Why
this
is
occurring
research
reasons
chapter.
Our
understanding
biology
system
has
increased
exponentially
with
advances
in
genomic
testing,
providing
further
opportunity
targeted
treatments
more
importantly,
primary
prevention
Clinical and Translational Medicine,
Journal Year:
2025,
Volume and Issue:
15(5)
Published: May 1, 2025
Abstract
Obesity
and
allergic
diseases
are
global
health
concerns,
both
of
which
seeing
an
increase
in
prevalence
recent
years.
has
been
recognised
as
important
comorbidity
subpopulations
with
airway
diseases,
represents
a
unique
phenotype
endotype.
Obesity‐related
associated
exacerbated
clinical
symptom
burden,
altered
immune
response,
increased
disease
severity
compromised
predictive
capability
conventional
biomarkers
for
evaluating
endotype
prognosis.
Moreover,
treatment
obesity‐related
is
challenging
because
this
poor
response
to
standard
therapeutic
strategies.
Therapeutic
regimen
that
involves
weight
loss
by
non‐surgical
surgical
interventions,
gut
microbiome‐targeted
treatment,
glucagon‐like
peptide‐1
receptor
agonist
other
agents
should
be
considered
population.
In
review,
we
outline
the
current
knowledge
impact
obesity
on
prevalence,
endotypes,
management
diseases.
Increased
understanding
implications
may
contribute
better
options
refractory
inflammation,
particularly
precision
medicine.
Key
points
can
such
asthma,
AR,
CRSwNP.
alters
exacerbates
symptoms
respiratory
exhibit
resistance
treatment.
constitute
distinct
category
endotypes
phenotypes,
requiring
further
in‐depth
research
novel
approaches.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: May 8, 2025
Although
infrequent,
there
have
been
Apollo
program
reports
of
lunar
dust
exposure
leading
to
notable
upper
respiratory
symptoms
in
select
crewmembers.
Possible
mechanisms
include
particulate
irritation,
inflammation
from
toxic
insult,
or
legitimate
adaptive
immune-mediated
response.
sterile
non-protein
matter
would
not
be
expected
immunogenic,
one
flight
surgeon
reported
increasing
upon
repeated
perceived
with
associated
eosinophilia,
suggestive
possible
allergic
reactions.
Many
International
Space
Station
(ISS)
crews
display
a
pattern
persistent
immune
system
dysregulation
and
latent
virus
reactivation.
Some
ISS
manifest
atypical
and/or
dermatitis
which
could
an
component.
It
is
logical
anticipate
crew
worsen
during
prolonged
deep
space
missions
planetary
surface
hazards
will
only
complicate
health
risks.
Allergic
(i.e.
mast
cell-mediated)
reactivity
adversely
increase
negative
clinical
operational
impacts
for
long-duration
astronauts
affect
countermeasure
requirements
vehicles.
This
study
investigated
whether
possibly
elicit
IgE
mediated
response
spaceflight
by
utilizing
vitro
cell
culture
models.
Our
laboratory
was
officially
approved
receipt
actual
samples
the
16
mission
NASA.
These
were
used
complete
proposed
set
experiments,
using
human
peripheral
blood
mononuclear
cells
(PBMC)
healthy
individuals,
basophils
eosinophil
lines.
Cells
co-cultured
cellular
mitogens,
common
recall
antigens
(Der
p1),
fine
ground
silica
quartz
(control),
dust,
alter
generation
selective
responses
Measured
outputs
included
supernatant-derived
total
IgE,
tryptase,
histamine,
selected
cytokine
levels.
Cellular
activation
monitored
assessing
markers
via
flow
cytometry.
EM/x-ray
analysis
determine
interactions
particles.
The
assessments
primary
indicated
no
evidence
responsiveness
nor
’allergy-like‘
dust.
Assessments
purified
’allergic‘
lines,
did
yield
some
unique
but
mild
however
such
lines
can
profiles
somewhat
different
their
vivo
counterparts.
determining
allergy
specific
responses,
help
guide
NASA
develop
mitigation
techniques
potential
countermeasures
necessary
event
excessive
EVAs.
International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(10), P. 4509 - 4509
Published: May 9, 2025
Allergic
rhinitis
(AR)
is
a
common
and
increasingly
prevalent
chronic
inflammatory
disorder
of
the
nasal
mucosa
that
severely
impacts
patients’
quality
life,
causing
symptoms
like
congestion,
sneezing,
itching.
AR
primarily
mediated
by
immunoglobulin
E
(IgE)
when
allergens
are
present,
making
it
challenging
to
manage
despite
available
therapies
pharmacotherapy,
immunotherapy,
surgery.
Recently,
research
has
focused
on
biologics
as
an
emerging
therapeutic
option
for
AR.
Biologics
target
specific
immune
pathways
in
type
2
inflammation,
which
underlies
many
allergic
diseases
including
offer
targeted
potentially
more
effective
alternative
traditional
therapies,
addressing
underlying
mechanisms
rather
than
simply
alleviating
symptoms.
Based
key
clinical
trial
evidence,
this
paper
tentatively
proposes
multidimensional
strategy
selecting
AR,
integrating
serum
IgE
levels,
disease
phenotypes
(seasonal/persistent),
comorbid
characteristics
guide
individualized
treatment.
However,
long-term
cost-effectiveness,
optimal
dosing
regimens,
patient
adherence
require
further
validation
through
real-world
data.
Despite
these
challenges,
recent
advancements
represent
promising
step
forward
management.
With
ongoing
trials,
may
soon
provide
lasting
relief
patients
suffering
from
rhinitis.