Scientific Reports,
Journal Year:
2024,
Volume and Issue:
14(1)
Published: May 17, 2024
The
relationship
between
the
Systemic
Inflammatory
Response
Index
(SIRI)
and
Fibrinogen-to-albumin
ratio
(FAR)
has
not
been
extensively
investigated.
objective
of
this
study
was
to
determine
independent
FAR
SIRI
in
people
with
osteoporotic
fractures
(OPF).
A
cross-sectional
conducted
using
retrospective
data
from
3431
hospitalized
OPF
patients.
exposure
variable
baseline
FAR,
while
outcome
SIRI.
Covariates,
including
age,
gender,
BMI,
other
clinical
laboratory
factors,
were
adjusted.
Cross-correlation
analysis
linear
regression
models
applied.
generalized
additive
model
(GAM)
investigated
non-linear
relationships.
Adjusted
revealed
an
negative
association
patients
(β
=
-
0.114,
p
0.00064,
95%
CI
0.180,
0.049).
substantial
U-shaped
shown
GAM
(p
<
0.001).
indicated
a
for
below
6.344%
positive
correlation
over
6.344%.
results
our
FAR.
lowest
conceivable
bone-loose
inflammatory
disease
might
be
6.344%,
suggesting
that
particular
significance
medical
diagnosis
therapy
persons
OPF.
Consequently,
term
"inflammatory
trough"
is
proposed.
These
offer
fresh
perspectives
on
controlling
inflammation
individuals
preventing
osteoporosis.
Viruses,
Journal Year:
2023,
Volume and Issue:
15(4), P. 865 - 865
Published: March 28, 2023
Τhe
COVID-19
pandemic
highly
impacted
the
circulation,
seasonality,
and
morbidity
burden
of
several
respiratory
viruses.
We
reviewed
published
cases
SARS-CoV-2
virus
co-infections
as
12
April
2022.
influenza
were
reported
almost
exclusively
during
first
wave.
It
is
possible
that
overall
incidence
higher
because
paucity
co-testing
for
viruses
waves
when
mild
might
have
been
missed.
Animal
models
indicate
severe
lung
pathology
high
fatality;
nevertheless,
available
literature
largely
inconclusive
regarding
clinical
course
prognosis
co-infected
patients.
also
importance
considering
sequence
timing
each
infection;
however,
there
no
such
information
in
human
cases.
Given
differences
between
2020
2023
terms
epidemiology
availability
vaccines
specific
treatment
against
COVID-19,
it
rational
not
to
extrapolate
these
early
findings
present
times.
expected
characteristics
will
evolve
upcoming
seasons.
Multiplex
real-time
PCR-based
assays
developed
past
two
years
should
be
used
increase
diagnostic
infection
control
capacity,
surveillance
purposes.
share
same
high-risk
groups,
essential
latter
get
vaccinated
both
Further
studies
are
needed
elucidate
how
shaped
years,
impact
prognosis.
Advanced Biotechnology,
Journal Year:
2025,
Volume and Issue:
3(1)
Published: Jan. 21, 2025
The
co-circulation
of
influenza
and
SARS-CoV-2
has
led
to
co-infection
events,
primarily
affecting
children
older
adults,
who
are
at
higher
risk
for
severe
disease.
Although
prevalence
is
relatively
low,
it
associated
with
worse
outcomes
compared
mono-infections.
Previous
studies
have
shown
that
the
depend
on
multiple
factors,
including
viral
interference,
virus-host
interaction
host
response.
Children
elderly
exhibit
distinct
patterns
antiviral
response,
which
involve
airway
epithelium,
mucociliary
clearance,
innate
adaptive
immune
cells,
inflammatory
mediators.
This
review
explores
pathogeneses
co-infection,
focusing
responses
in
elderly.
By
comparing
immature
immunity
senescence
we
aim
provide
insights
clinical
management
cases.
Journal of Virology,
Journal Year:
2022,
Volume and Issue:
96(15)
Published: July 12, 2022
Severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
and
influenza
A
virus
(IAV)
represent
two
highly
transmissible
airborne
pathogens
with
pandemic
capabilities.
Although
these
viruses
belong
to
separate
families-SARS-CoV-2
is
a
member
of
the
family
Coronaviridae,
while
IAV
Orthomyxoviridae-both
have
shown
zoonotic
potential,
significant
animal
reservoirs
in
species
close
contact
humans.
The
are
similar
their
capacity
infect
human
airways,
coinfections
resulting
morbidity
mortality
been
documented.
Here,
we
investigate
interaction
between
SARS-CoV-2
USA-WA1/2020
H1N1
A/California/04/2009
during
coinfection.
Competition
assays
vitro
were
performed
susceptible
cells
that
either
interferon
type
I/III
(IFN-I/-III)
nonresponsive
or
IFN-I/-III
responsive,
addition
an
vivo
golden
hamster
model.
We
find
infection
does
not
interfere
biology
vivo,
regardless
timing
infections.
In
contrast,
observe
loss
replication
following
infection.
latter
phenotype
correlates
increased
levels
immune
priming
interferes
kinetics
replication.
Together,
data
suggest
cocirculation
unlikely
result
severity
disease.
IMPORTANCE
population
now
has
circulating
RNA
high
namely,
virus.
As
both
airways
can
mortality,
it
imperative
also
understand
consequences
getting
coinfected.
demonstrate
host
response
uniquely
although
inverse
relationship
evident.
Overall,
comparable
alone.
Viruses,
Journal Year:
2024,
Volume and Issue:
16(6), P. 863 - 863
Published: May 28, 2024
COVID-19
is
a
spectrum
of
clinical
symptoms
in
humans
caused
by
infection
with
SARS-CoV-2.
The
coalescence
SARS-CoV-2
seasonal
respiratory
viruses,
particularly
influenza
global
health
concern.
To
understand
this,
transgenic
mice
expressing
the
human
ACE2
receptor
(K18-hACE2)
were
infected
A
virus
(IAV)
followed
and
host
response
effect
on
biology
was
compared
to
K18-hACE2
IAV
or
alone.
sequentially
showed
reduced
RNA
synthesis,
yet
exhibited
more
rapid
weight
loss,
severe
lung
damage
prolongation
innate
singly
control
mice.
Sequential
also
exacerbated
extrapulmonary
encephalitic
manifestations
associated
infection.
Conversely,
prior
commercially
available,
multivalent
live-attenuated
vaccine
(Fluenz
Tetra)
elicited
same
reduction
albeit
without
increase
disease
severity.
This
suggests
that
immune
stimulated
inhibits
Interestingly,
an
attenuated,
apathogenic
does
not
result
aberrant
enhanced
Taken
together,
data
suggest
coinfection
(‘twinfection’)
deleterious
mitigation
steps
should
be
instituted
as
part
comprehensive
public
management
strategy
COVID-19.
Pathogens,
Journal Year:
2024,
Volume and Issue:
13(4), P. 316 - 316
Published: April 12, 2024
Respiratory
viral
coinfections
are
a
global
public
health
threat
that
poses
an
economic
burden
on
individuals,
families,
and
healthcare
infrastructure.
Viruses
may
coinfect
interact
synergistically
or
antagonistically,
their
coinfection
not
affect
replication
rate.
These
interactions
specific
to
different
virus
combinations,
which
underlines
the
importance
of
understanding
mechanisms
behind
these
differential
need
for
novel
diagnostic
methods
accurately
identify
multiple
viruses
causing
disease
in
patient
avoid
misdiagnosis.
This
review
examines
epidemiological
patterns,
pathology
manifestations,
immune
response
modulation
respiratory
combinations
occur
during
using
experimental
models
better
understand
dynamics
takes
driving
outcomes
severity,
is
crucial
guide
development
prevention
treatment
strategies.
PLoS Pathogens,
Journal Year:
2023,
Volume and Issue:
19(3), P. e1011167 - e1011167
Published: March 8, 2023
Despite
the
availability
of
effective
vaccines,
persistence
severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
suggests
that
cocirculation
with
other
pathogens
and
resulting
multiepidemics
(of,
for
example,
COVID-19
influenza)
may
become
increasingly
frequent.
To
better
forecast
control
risk
such
multiepidemics,
it
is
essential
to
elucidate
potential
interactions
SARS-CoV-2
pathogens;
these
interactions,
however,
remain
poorly
defined.
Here,
we
aimed
review
current
body
evidence
about
interactions.
Our
structured
in
four
parts.
study
pathogen
a
systematic
comprehensive
way,
first
developed
general
framework
capture
their
major
components:
sign
(either
negative
antagonistic
or
positive
synergistic
interactions),
strength
(i.e.,
magnitude
interaction),
symmetry
(describing
whether
interaction
depends
on
order
infection
interacting
pathogens),
duration
short-lived
long-lived),
mechanism
(e.g.,
modifies
susceptibility
infection,
transmissibility
severity
disease).
Second,
reviewed
experimental
from
animal
models
Of
14
studies
identified,
11
focused
outcomes
coinfection
nonattenuated
influenza
A
viruses
(IAVs),
3
pathogens.
The
IAV
used
different
designs
(ferrets,
hamsters,
mice)
but
generally
demonstrated
increased
disease
compared
either
monoinfection.
By
contrast,
effect
viral
load
virus
was
variable
inconsistent
across
studies.
Third,
epidemiological
human
populations.
Although
numerous
were
only
few
specifically
designed
infer
interaction,
many
prone
multiple
biases,
including
confounding.
Nevertheless,
results
suggested
pneumococcal
conjugate
vaccinations
associated
reduced
infection.
Finally,
fourth,
formulated
simple
transmission
an
epidemic
endemic
bacterial
pathogen,
showing
how
they
can
naturally
incorporate
proposed
framework.
More
generally,
argue
models,
when
integrative
multidisciplinary
perspective,
will
be
invaluable
tools
resolve
substantial
uncertainties
The Journal of Infectious Diseases,
Journal Year:
2023,
Volume and Issue:
229(5), P. 1430 - 1434
Published: Sept. 18, 2023
Abstract
To
gain
insight
into
interactions
among
respiratory
viruses,
we
modeled
influenza
A
virus
(IAV)-severe
acute
syndrome
coronavirus
2
(SARS-CoV-2)
coinfections
using
differentiated
human
airway
epithelial
cultures.
Replicating
IAV
induced
a
more
robust
interferon
response
than
SARS-CoV-2
and
suppressed
replication
in
both
sequential
simultaneous
infections,
whereas
did
not
enhance
host
cell
defense
during
infection
or
suppress
replication.
Oseltamivir,
an
antiviral
targeting
influenza,
reduced
coinfection
but
also
the
restored
These
results
demonstrate
how
perturbations
one
viral
can
impact
its
effect
on
coinfecting
virus.
Analytical Chemistry,
Journal Year:
2024,
Volume and Issue:
96(4), P. 1725 - 1732
Published: Jan. 19, 2024
Various
platforms
for
the
accurate
diagnosis
of
infectious
diseases
have
been
studied
because
emergence
coronavirus
disease
(COVID-19)
in
2019.
Recently,
it
has
become
difficult
to
distinguish
viruses
with
similar
symptoms
due
continuous
mutation
viruses,
and
there
is
an
increasing
need
a
diagnostic
method
detect
them
simultaneously.
Therefore,
we
developed
paper-based
rapid
antigen
test
using
DNA
aptamers
simultaneous
detection
influenza
A,
B,
COVID-19.
Aptamers
specific
each
target
viral
were
selected
attached
AuNPs
application
kit
our
company's
heterogeneous
sandwich-type
aptamer
screening
(H-SELEX).
We
confirmed
that
three
could
be
detected
on
same
membrane
without
cross-reactivity
based
high
stability,
specificity,
binding
affinity
aptamers.
Further,
limit
was
2.89
pg·mL–1
when
applied
develop
signal
amplification
technology;
virus
successfully
diluted
nasopharyngeal
samples.
believe
kit,
such
accuracy,
can
various
diseases,
thereby
therapeutic
effect
contributing
clinical
field.
The Journal of Experimental Medicine,
Journal Year:
2024,
Volume and Issue:
221(9)
Published: July 1, 2024
Studies
during
the
COVID-19
pandemic
showed
that
children
had
heightened
nasal
innate
immune
responses
compared
with
adults.
To
evaluate
role
of
viruses
and
bacteria
in
driving
these
responses,
we
performed
cytokine
profiling
comprehensive,
symptom-agnostic
testing
for
respiratory
bacterial
pathobionts
nasopharyngeal
samples
from
tested
SARS-CoV-2
2021-22
(n
=
467).
Respiratory
and/or
were
highly
prevalent
(82%
symptomatic
30%
asymptomatic
children;
90
49%
<5
years).
Virus
detection
load
correlated
interferon
response
biomarker
CXCL10,
previously
reported
discrepancy
between
viral
was
explained
by
coinfections.
Bacterial
a
distinct
proinflammatory
elevated
IL-1β
TNF
but
not
CXCL10.
Furthermore,
paired
healthy
1-year-olds
collected
1-2
wk
apart
revealed
frequent
virus
acquisition
or
clearance,
mucosal
immunophenotype
changing
parallel.
These
findings
reveal
frequent,
dynamic
host-pathogen
interactions
drive
activation
children.