Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: Oct. 18, 2024
This
study
aimed
to
investigate
the
potential
relationship
between
multiple
sclerosis
(MS)
and
coronavirus
disease
2019
(COVID-19)
outcomes
using
Mendelian
randomization
analysis.
Specifically,
it
evaluates
whether
genetic
factors,
including
single-nucleotide
polymorphism
(SNP)
rs10191329,
influence
susceptibility
of
MS
patients
three
COVID-19
[severe
acute
respiratory
syndrome
2
(SARS-CoV-2)
infection,
hospitalized
COVID-19,
severe
COVID-19].
utilized
genome-wide
association
summary
statistics
from
International
Multiple
Sclerosis
Genetics
Consortium
conduct
a
SNPs
strongly
associated
with
were
selected
examine
their
impact
on
outcomes.
The
analysis
focused
identifying
any
causal
associations
severity,
as
well
assessing
role
interferon
beta
(IFNβ)
treatment
in
modifying
these
results
suggest
an
increased
risk
but
individuals
carrying
rs10191329
SNP
appeared
less
likely
develop
COVID-19.
SNP,
located
within
DYSF-ZNF638
locus,
may
immune
responses
highlighting
its
relevance
for
personalized
strategies.
Importantly,
no
significant
was
found
IFNβ
outcomes,
indicating
that
findings
treated
differ
those
observed
untreated
patients.
suggests
offer
protective
effects
against
SARS-CoV-2
These
underscore
importance
such
shaping
clinical
context
Further
research
should
explore
targeted
therapies
approaches
managing
during
ongoing
pandemic.
Heliyon,
Journal Year:
2025,
Volume and Issue:
11(4), P. e42739 - e42739
Published: Feb. 1, 2025
This
review
explores
the
synergistic
potential
of
natural
products
and
nanotechnology
for
viral
infections,
highlighting
key
antiviral,
immunomodulatory,
antioxidant
properties
to
combat
pandemics
caused
by
highly
infectious
viruses.
These
often
result
in
severe
public
health
crises,
particularly
affecting
vulnerable
populations
due
respiratory
complications
increased
mortality
rates.
A
cytokine
storm
is
initiated
when
an
overload
pro-inflammatory
cytokines
chemokines
released,
leading
a
systemic
inflammatory
response.
Viral
mutations
limited
availability
effective
drugs,
vaccines,
therapies
contribute
continuous
transmission
virus.
The
coronavirus
disease-19
(COVID-19)
pandemic
has
sparked
renewed
interest
product-derived
antivirals.
efficacy
traditional
medicines
against
infections
examined.
Their
anti-inflammatory,
are
highlighted.
discusses
how
enhances
herbal
combating
infections.
Trends in Immunology,
Journal Year:
2024,
Volume and Issue:
45(8), P. 609 - 624
Published: July 20, 2024
Recent
studies
show
an
important
role
for
non-neutralizing
anti-spike
antibodies,
including
monoclonal
antibodies
(mAbs),
in
robustly
protecting
against
SARS-CoV-2
infection.
These
mAbs
use
Fc-mediated
functions
such
as
complement
activation,
phagocytosis,
and
cellular
cytotoxicity.
There
is
untapped
potential
using
durable
antibody
treatments;
because
of
their
available
conserved
epitopes,
they
may
not
be
sensitive
to
virus
mutations
neutralizing
mAbs.
Here,
we
discuss
evidence
mAb-mediated
protection
We
explore
how
mAb
can
enhanced
via
novel
antibody-engineering
techniques.
Important
questions
remain
answered
regarding
the
characteristics
protective
mAbs,
models
assays
used
study,
risks
ensuing
detrimental
inflammation,
well
durability
mechanisms
protection.
Immunity & Ageing,
Journal Year:
2025,
Volume and Issue:
22(1)
Published: March 12, 2025
Epidemiological
investigations
consistently
demonstrate
an
overrepresentation
of
the
elderly
in
COVID-19
hospitalizations
and
fatalities,
making
advanced
age
as
a
major
predictor
disease
severity.
Despite
this,
comprehensive
understanding
cellular
molecular
mechanisms
explaining
how
old
represents
risk
factor
remain
elusive.
To
investigate
we
compared
SARS-CoV-2
infection
outcomes
young
adults
(2
months)
geriatric
(15–22
mice.
Both
groups
K18-ACE2
mice
were
intranasally
infected
with
500
TCID50
Delta
variant
analyses
performed
on
days
3,
5,
7
post-infection
(DPI).
Analyses
included
pulmonary
cytokines,
lung
RNA-seq,
viral
loads,
lipidomic
profiles,
histological
assessments,
concurrent
evaluation
percentage
reaching
humane
endpoints.
The
findings
unveiled
notable
differences,
aged
exhibiting
impaired
clearance,
reduced
survival,
failure
to
recover
weight
loss
due
infection.
RNA-seq
data
suggested
greater
damage
respiratory
function
Additionally,
elderly-infected
exhibited
deficient
antiviral
response
characterized
by
Th1-associated
mediators
(IFNγ,
CCL2,
CCL3,
CXCL9)
diminished
number
macrophages,
NK
cells,
T
cells.
Furthermore,
mass-spectrometry
analysis
lipidome
indicated
altered
expression
several
lipids
immunomodulatory
pro-resolution
effects
such
Resolvin,
HOTrEs,
NeuroP,
but
also
DiHOMEs-related
ARDS.
These
indicate
that
aging
affects
immunity,
leading
prolonged
infection,
damage,
poorer
clinical
outcomes.
This
underscores
potential
efficacy
treatments
for
subjects
experiencing
symptoms
severe
COVID-19.
Brain Behavior & Immunity - Health,
Journal Year:
2025,
Volume and Issue:
unknown, P. 100983 - 100983
Published: March 1, 2025
The
acute
and
post-acute
sequelae
of
SARS-CoV-2
infection
have
been
great
clinical
interest
since
the
inception
COVID-19
pandemic.
Despite
a
high
prevalence
individuals
with
persistent
symptoms,
wholistic
view
effects
on
special
sensory
systems
is
lacking.
Considering
significant
impact
normal
function
quality
life,
goal
this
review
to
highlight
unresolved
issues
related
SARS-CoV-2-associated
insults
nervous
system.
In
narrative
review,
we
discuss
epidemiology
SARS-CoV-2-induced
perturbations,
underlying
pathological
mechanisms,
possible
therapeutic
strategies
across
olfactory,
gustatory,
somatosensory,
visual,
auditory
systems.
Examined
literature
included
studies
human
biospecimens,
human-derived
cell
lines,
naturally
susceptible
animal
models,
which
highlighted
evidence
functional
disruption
in
all
was
associated
inflammation
olfactory
epithelium/bulb,
somatosensory
ganglia,
gustatory
systems,
long-term
transcriptional
perturbations
central
system
peripheral
system,
detectable
degeneration/apoptosis
visual
Few
proposed
evidence-based
for
attenuating
specific
abnormalities
after
infection.
While
some
extent
more
thoroughly
investigated
from
symptomatology,
behavioral
molecular
perspectives,
there
still
an
unmet
need
development
therapeutics
treat
COVID-induced
impairment
these
Further,
additional
attention
must
be
placed
COVID-associated
lack
detailed
mechanistic
investigations
into
their
pathogenesis.
Viruses,
Journal Year:
2025,
Volume and Issue:
17(4), P. 500 - 500
Published: March 30, 2025
The
global
impact
of
the
COVID-19
pandemic,
caused
by
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2),
persists
in
part
due
to
emergence
new
variants.
Understanding
variant-specific
infection
dynamics
and
pathogenesis
murine
models
is
crucial
for
identifying
phenotypic
changes
guiding
development
countermeasures.
To
address
limitations
earlier
studies
that
investigated
only
a
few
variants
or
used
small
sample
sizes,
we
evaluated
clinical
disease,
kinetics,
viral
titers,
cellular
localization,
histopathologic
lungs
brains
transgenic
B6.Cg-Tg(K18-ACE2)2Prlmn/J
(“K18”)
corresponding
genetic
control
(C57BL/6J)
mice
expressing
human
angiotensin-converting
enzyme
(hACE2).
Six
SARS-CoV-2
were
assessed:
B.1
(WA1-like),
alpha,
beta,
delta,
omicron,
omicron
XBB.1.5,
using
cohorts
≥18
mice.
Following
intranasal
inoculation
with
B.1,
delta
variants,
K18
experienced
rapid
weight
loss
reached
euthanasia
criteria
5–6
days
post-inoculation
(dpi).
In
contrast,
inoculated
both
recovered
their
starting
within
4–6
dpi.
Infectious
was
detected
oropharynx
at
1
and2
dpi,
2,
4,
6
brain
4
dpi
all
except
omicron.
nucleoprotein
detected,
interstitial
pneumonia
varying
severity
observed
infected
Brain
lesions
identified
As
express
hACE2
brain—a
feature
not
present
humans—we
also
compared
three
those
mouse-adapted
WA1
strain
C57BL/6J
lacking
ACE2
gene.
did
experience
lethal
exhibited
milder
pneumonia,
had
no
evidence
neuroinvasion
despite
similar
kinetics
These
findings
demonstrate
contrasting
phenotypes
across
two
reduced
tropism
pathology
models.
This
comprehensive
analysis
mouse
provides
valuable
insights
model
variant
selection
future
studies.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: April 4, 2025
The
host
complement
system
is
a
critical
component
of
innate
immunity
and
serves
as
principal
mechanism
pathogen
defense
in
mammals.
EP67
an
engineered
decapeptide
derived
from
the
C
terminus
human
protein
C5a,
which
displays
selective
immunostimulatory
activity.
preferentially
activates
phagocyte
mononuclear
cells
but
shows
minimal
activity
towards
inflammatory
granulocytes,
including
neutrophils.
Previous
studies
viral
infection
showed
that
possessed
antiviral
efficacy
when
used
following
enhanced
antibody
responses
to
antigen
challenges
adjuvant.
Here,
we
show
rodent
model
immunization
with
inactivated
γ-irradiated
SARS-CoV-2
combination
can
produce
elevated
nucleocapsid-specific
IgG
antibodies
compared
lysate
alone,
supporting
adaptive
immune
response.
Additionally,
intranasal
administration
live
MHV-A59
coronavirus
resulted
rapid
health
improvement
symptomatic
infections
PBS
vehicle
controls.
Taken
together,
these
results
suggest
betacoronaviruses
adjuvant
during
or
therapeutic
active
infections.
Moreover,
findings
continue
support
capability
agent
useful
peptide.
PLoS Pathogens,
Journal Year:
2024,
Volume and Issue:
20(8), P. e1012439 - e1012439
Published: Aug. 12, 2024
Natural
killer
(NK)
cells
play
a
critical
role
in
virus
control.
However,
it
has
remained
largely
unclear
whether
NK
cell
mobilization
SARS-CoV-2
infections
is
beneficial
or
pathologic.
To
address
this
deficit,
we
employed
validated
experimental
depletion
non-human
primate
(NHP)
model
with
Delta
variant
B.1.617.2
challenge.
Viral
loads
(VL),
numbers,
activation,
proliferation,
and
functional
measures
were
evaluated
blood
tissues.
In
non-depleted
(control)
animals,
infection
rapidly
induced
expansion,
increased
tissue
trafficking
associated
VL.
Strikingly,
report
that
leads
to
higher
VL,
longer
duration
of
viral
shedding,
significantly
levels
pro-inflammatory
cytokines
the
lungs,
overt
lung
damage.
Overall,
find
first
significant
conclusive
evidence
for
cell-mediated
control
replication
disease
pathology.
These
data
indicate
adjunct
therapies
could
benefit
from
cell-targeted
approaches.