International Journal of Molecular Sciences,
Год журнала:
2024,
Номер
25(24), С. 13613 - 13613
Опубликована: Дек. 19, 2024
This
longitudinal
study
examined
how
active
gastrointestinal
(GI)
cancer
types
affect
immune
responses
to
SARS-CoV-2,
focusing
on
the
ability
neutralize
Omicron
variants.
Patients
with
GI
(n
=
168)
were
categorized
into
those
hepatocellular
carcinoma,
hepatic
metastatic
cancer,
non-hepatic
and
two
control
groups
of
patients
without
underlying
liver
diseases.
Humoral
cellular
evaluated
before
after
antigen
exposures.
In
pre-Omicron
era,
humoral
SARS-CoV-2
immunity
decreased
three
contacts
further
exposure.
While
neutralization
was
significantly
lower
than
wildtype
(p
<
0.01),
infections
yet
mild
moderate.
Additional
exposures
improved
IgG
levels
0.01)
0.01).
However,
this
effect
less
intense
in
particularly
pancreaticobiliary
neoplasms
(PBN;
p
0.04),
immunodeficiency
0.05),
and/or
under
conventional
chemotherapy
0.05).
Pre-Omicron
prevented
severe
clinical
courses
variants
cancer.
PBN,
immunodeficiency,
initial
antigens
triggered
only
reduced
responses.
Thus,
subgroups
could
be
identified
for
whom
booster
vaccinations
are
special
significance.
Research Square (Research Square),
Год журнала:
2024,
Номер
unknown
Опубликована: Окт. 17, 2024
Abstract
Objective
This
study
aimed
to
investigate
the
clearance
of
SARS-CoV-2
in
people
living
with
HIV
(PLWH)
after
receiving
anti-SARS-CoV-2
treatment
and
relevant
factors.
Methods
A
retrospective
investigation
was
conducted
based
on
clinical
data
patients
between
December
2022
June
2023.
The
were
categorized
into
PLWH
HIV-negative
groups.
Basic
information,
comorbidity,
COVID-19
severity,
white
blood
cell
count,
lymphocyte
medicine,
steroid
usage,
virus
shedding
duration
collected.
Kaplan-Meier
curve
employed
compare
rates,
multivariate
logistic
regression
Cox
analyses
utilized
identify
factors
influencing
duration.
Results
total
149
(32
117
individuals)
enrolled
study.
median
estimated
for
group
are
21
days
14
days,
respectively
(P
<
0.001).
rates
at
5th
day
15.63%
60.68%
0.001),
28th
87.50%
97.44%
=
0.019)
groups,
respectively.
Multivariate
analysis
showed
that
infection
(OR
0.026,
95%
CI:
0.004–0.159)
count
admission
4.341,
1.536–12.265)
independent
0.05).
Compared
mild
group,
moderate
severe
groups
had
significant
impacts
both
revealed
age
0.977,
0.963–0.991),
0.351,
0.197–0.626),
therapy
initiation
0.827,
0.786–0.871),
1.999,
1.372–2.914)
moderate,
severe,
critically
ill
statistically
nucleic
acid
conversion
Conclusion
a
prolonged
even
treatment,
which
could
lead
more
opportunities
accumulate
multiple
mutations
induce
resistance
medicines.
Antimicrobial Agents and Chemotherapy,
Год журнала:
2024,
Номер
unknown
Опубликована: Дек. 17, 2024
ABSTRACT
Novel
and
repurposed
antiviral
drugs
are
available
for
the
treatment
of
coronavirus
disease
2019
(COVID-19).
However,
combinations
may
be
more
potent
lead
to
faster
viral
clearance,
but
methods
screening
against
respiratory
viruses
not
well
established
labor-intensive.
Here,
we
describe
a
time-efficient
(72–96
h)
simple
in
vitro
drug-sensitivity
assay
severe
acute
syndrome
2
(SARS-CoV-2)
using
standard
96-well
plates.
We
employ
different
synergy
models
(zero
interaction
potency,
highest
single
agent,
Loewe,
Bliss)
determine
efficacy
therapies
synergistic
ancestral
emerging
clinical
SARS-CoV-2
strains.
found
that
monotherapy
remdesivir,
nirmatrelvir,
active
metabolite
molnupiravir
(EIDD-1931)
demonstrated
baseline
EC50s
within
clinically
achievable
levels
4.34
mg/L
(CI:
3.74–4.94
mg/L),
1.25
1.10–1.45
0.25
0.20–0.30
respectively,
strain.
their
varied
newer
Omicron
variants
BA.1.1.15
BA.2,
particularly
with
protease
inhibitor
nirmatrelvir.
also
remdesivir
nirmatrelvir
have
consistent,
strong
effect
(Bliss
score
>10)
at
relevant
drug
concentrations
(nirmatrelvir
0.25–1
1–4
mg/L)
across
all
strains
tested.
This
method
offers
practical
tool
streamlines
identification
effective
combination
detection
resistance.
Our
findings
support
use
targeting
multiple
components
enhance
COVID-19
efficacy,
context
International Journal of Molecular Sciences,
Год журнала:
2024,
Номер
25(24), С. 13613 - 13613
Опубликована: Дек. 19, 2024
This
longitudinal
study
examined
how
active
gastrointestinal
(GI)
cancer
types
affect
immune
responses
to
SARS-CoV-2,
focusing
on
the
ability
neutralize
Omicron
variants.
Patients
with
GI
(n
=
168)
were
categorized
into
those
hepatocellular
carcinoma,
hepatic
metastatic
cancer,
non-hepatic
and
two
control
groups
of
patients
without
underlying
liver
diseases.
Humoral
cellular
evaluated
before
after
antigen
exposures.
In
pre-Omicron
era,
humoral
SARS-CoV-2
immunity
decreased
three
contacts
further
exposure.
While
neutralization
was
significantly
lower
than
wildtype
(p
<
0.01),
infections
yet
mild
moderate.
Additional
exposures
improved
IgG
levels
0.01)
0.01).
However,
this
effect
less
intense
in
particularly
pancreaticobiliary
neoplasms
(PBN;
p
0.04),
immunodeficiency
0.05),
and/or
under
conventional
chemotherapy
0.05).
Pre-Omicron
prevented
severe
clinical
courses
variants
cancer.
PBN,
immunodeficiency,
initial
antigens
triggered
only
reduced
responses.
Thus,
subgroups
could
be
identified
for
whom
booster
vaccinations
are
special
significance.