Rheumatology Science and Practice,
Journal Year:
2024,
Volume and Issue:
62(5), P. 465 - 473
Published: Oct. 31, 2024
Patients
with
ANCA-associated
systemic
vasculitis
(AAV)
are
at
risk
of
severe
COVID-19.
At
the
same
time,
in
immunocompromised
patients,
particular
those
receiving
anti-B
cell
therapy
rituximab
(RTX),
post-vaccination
effect
may
be
insufficient.
Since
2022
long-acting
virus-neutralizing
monoclonal
antibodies
(MAB)
tixagevimab
and
cilgavimab
(Evushheld,
AZD7442)
have
been
used
as
pre-exposure
prophylaxis
for
The
aim
study
is
to
evaluate
effectiveness
(TC)
COVID-19
its
safety
RTX
treated
patients
AAV.
Materials
methods
.
prospective
included
63
AAV
RTX.
Median
age
53
(19–
79)
years,
M:F
1:1.1.
From
March
June
2023,
TC
was
administered
a
total
dose
300
mg
and/or
600
mg.
Observation
continued
until
April
2024.
In
November
2023
2024
telephone
online
survey
conducted
simultaneously
identify
confirmed
cases
adverse
reactions.
also
Treatment
Satisfaction
Questionnaire
version
9
(TSQM-9).
Considering
duration
(6
months),
were
divided
into
two
groups
depending
on
interval
after
last
administration
TC:
up
6
months
inclusive
–
group
1;
more
than
2.
Results
During
two-year
follow-up
period,
detected
31.7%
median
between
development
5.5
[2–19]
months.
1,
which
12
COVID-19,
92%
had
mild
form
disease,
only
one
lung
damage,
there
no
fatal
outcomes.
2,
cessation
accompanied
by
damage
89%
cases,
required
hospitalization
78%,
patients.
Four
prolonged
course
persistence
SARS-CoV-2
(pCOVID,
persistent
COVID).
4
including
3
pCOVID,
treatment
carried
out
combined
antiviral
drug
nirmarelvir
+
ritonavir
(Skyvira)
combination
intravenous
human
immunoglobulin
(IVIG)
effect.
There
statistically
significant
differences
incidence
secondary
immunodeficiency
without
it
(p=0.868).
final
stage
study,
serum
level
IgG
examined
34
70.4
(0.33–1086.1)
binding
antibody
units
(BAU),
indicates
lack
neutralizing
most
patients;
statistical
their
(p=0.685).
No
reactions
directly
related
use
observed.
A
high
TSQM-9
global
satisfaction
domain
noted
71.4
(14.3–100);
72,4%
respondents
answered
“satisfied”–
“extremely
satisfied”
first
question
(effectiveness
domain).
Conclusions
Pre-exposure
using
RTM
safe
allowed
reduce
avoid
deaths
during
period
action.
After
TC,
an
increase
frequency
need
observed,
pCOVID
noted.
Skyvira
IVIG
effective
all
cases.
MAB
other
rheumatic
diseases
requires
further
in-depth
study.
Viruses,
Journal Year:
2025,
Volume and Issue:
17(2), P. 147 - 147
Published: Jan. 23, 2025
In
a
patient
on
immunosuppressant
treatment,
SARS-CoV-2
RNA
was
documented
in
different
extra-respiratory
samples
over
several
months
the
absence
of
positive
determinations
upper
respiratory
samples.
Whole-genome
sequencing
these
showed
acquisition
single-nucleotide
polymorphisms
time,
suggesting
viral
evolution
and
thus
viability.
Research Square (Research Square),
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 3, 2025
Abstract
COVID-19
associated
coagulation
abnormalities
and
thrombosis
are
life-threatening
complications
after
SARS-CoV-2
infection.
However,
the
underlying
mechanisms
unclear.
Here,
we
found
that
spike
(S)
protein
induced
excessive
reactive
oxygen
species
(ROS)
production,
disrupting
mitochondrial
dynamics
causing
endothelial
cells
damage,
thereby
promoting
thrombogenesis.
Mechanistically,
S
inhibited
expression
of
signaling
lymphocytic
activation
molecule
family
8
(SLAMF8)
to
induce
an
upregulation
NADPH
oxidase
2
(NOX2)
p66SHC
phosphorylation.
This
NOX2-p66SHC
axis
resulted
in
a
persistent
elevation
ROS
disorder,
ultimately
leading
injury.
infection
also
promoted
transformation
into
prothrombotic
phenotype
by
inhibiting
SLAMF8.
Furthermore,
single-cell
sequencing
analysis
revealed
negative
correlation
between
SLAMF8
thrombotic
activity
patients.
Notably,
overexpression
reversed
protein-mediated
increase
blood
flow
obstruction
platelet
aggregation
observed
mice
with
ferric
chloride-induced
thrombosis.
These
findings
suggest
distinct
mechanism
pathogenesis
SARS-CoV-2-associated
thrombosis,
providing
novel
perspectives
strategies
for
prevention,
management
treatment
individuals
or
long
COVID.
Journal of Antimicrobial Chemotherapy,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 13, 2025
Abstract
Background
Persistent
COVID-19
(pCOVID-19)
in
immunocompromised
patients
is
characterized
by
unspecific
symptoms
and
pulmonary
infiltrates
due
to
ongoing
severe
acute
respiratory
syndrome
coronavirus-2
(SARS-CoV-2)
replication.
Treatment
options
remain
unclear,
leading
different
approaches,
including
combination
therapy
extended
durations.
The
purpose
of
this
study
was
assess
the
efficacy
safety
antiviral
therapies
for
pCOVID-19
since
Omicron
surge.
Methods
We
searched
MEDLINE
Scopus
from
1
January
2022
6
August
2024
cohort
studies
case
series
on
nirmatrelvir/ritonavir,
remdesivir,
ensitrelvir
molnupiravir.
Evidence
certainty
rated
using
Grading
Recommendations
Assessment,
Development,
Evaluation
outcomes
viral
clearance,
recurrence/relapse,
mortality,
adverse
events
(AEs)
symptom
resolution.
Results
Thirteen
involving
127
cases
were
included.
very
low.
In
with
at
least
two
direct
agents,
clearance
79%,
a
16%
recurrence
rate.
All-cause
mortality
9%,
6%
while
SARS-CoV-2
positive.
47
cases,
AEs
reported
11%.
Symptom
resolution
ranged
3
days
studies.
one
agent
passive
immunization,
89%,
an
11%
rate
no
deaths.
four
documented
observed.
monotherapy,
100%,
15%
One
death,
unrelated
SARS-CoV-2,
occurred.
12
Conclusions
Based
low
evidence,
combining
immunization
resulted
high
rates
few
recurrences.
occurred
treated
antivirals.
Controlled
are
needed.
Viruses,
Journal Year:
2025,
Volume and Issue:
17(2), P. 182 - 182
Published: Jan. 27, 2025
The
SARS-CoV-2-induced
disease,
COVID-19,
remains
a
worldwide
public
health
concern
due
to
its
high
rate
of
transmission,
even
in
vaccinated
and
previously
infected
people.
In
the
endemic
state,
it
continues
cause
significant
pathology.
To
elu-
cidate
viral
mutational
changes
screen
emergence
new
variants
concern,
we
conducted
this
study
Bangladesh.
RNA
genomes
extracted
from
25
ran-
domly
collected
samples
COVID-19-positive
patients
March
2021
February
2022
were
sequenced
using
Illumina
COVID
Seq
protocol
genomic
data
processing,
as
well
evaluations
performed
DRAGEN
Lineage
software.
study,
percentage
Delta,
Omicron,
Mauritius
identified
88%,
8%,
4%,
respectively.
All
had
23,403
A>G
(D614G,
S
gene),
3037
C>T
(nsp3),
14,408
(nsp12)
mutations,
where
was
responsible
for
increased
transmis-
sion.
Omicron
highest
number
unique
mutations
spike
protein
(i.e.,
sub-
stitutions,
deletions,
insertions),
which
may
explain
higher
transmissibility
immune-evading
ability
than
Delta.
A
total
779
identified,
691
substitutions,
85
3
insertion
observed.
sum
up,
our
will
enrich
database
SARS-CoV-2,
aiding
treatment
strategies
along
with
understanding
virus’s
preferences
both
mutation
type
site
predicting
newly
emerged
viruses’
survival
thus
preparing
coun-
teract
them.
BMC Infectious Diseases,
Journal Year:
2025,
Volume and Issue:
25(1)
Published: April 28, 2025
Immunocompromised
(IC)
patients
face
significant
challenges
in
managing
COVID-19
due
to
their
heightened
susceptibility
severe
illness,
persistent
infections,
and
the
potential
development
of
drug
resistance.
Studies
indicate
that
IC
patients,
particularly
those
with
hematologic
malignancies
(HM),
hematopoietic
stem
cell
transplants
(HSCTR),
or
solid
organ
(SOTR),
experience
higher
mortality
rates
worse
outcomes
compared
general
population,
even
post-vaccination.
The
persistence
virus
these
combined
its
rapid
mutation,
further
complicates
treatment.
Recent
evidence
supports
use
neutralizing
monoclonal
antibodies
(mAbs)
direct-acting
antivirals
(DAAs)
as
a
more
effective
approach
viral
clearance,
reducing
mortality,
preventing
relapses.
However,
rise
resistant
variants,
especially
mAbs,
concerns
about
safety
prolonged
intensive
therapies
pose
ongoing
challenges.
Monotherapies
often
fail
short
address
issues,
highlighting
need
for
early
therapy
(ECT)
mAbs
DAAs.
ECT
has
shown
promise
individuals
by
targeting
multiple
stages
lifecycle,
load,
clearing
infections
at
earlier
stages,
which
helps
mitigate
risks
disease
Continued
research
is
essential
refine
treatment
protocols,
evolves.
Although
studies
are
needed,
current
findings
suggest
may
become
standard
care
severely
offering
better
clinical
hindering
persistence.