Ursodeoxycholic acid does not reduce SARS-CoV-2 infection in newly allogeneic hematopoietic stem cell transplantation recipients: a prospective NICHE cohort
Hongye Gao,
No information about this author
Jiali Wang,
No information about this author
Xinhui Zheng
No information about this author
et al.
Frontiers in Cellular and Infection Microbiology,
Journal Year:
2024,
Volume and Issue:
14
Published: March 5, 2024
Introduction
Retrospective
studies
have
suggested
that
Ursodeoxycholic
Acid
(UDCA)
provide
a
protective
effect
against
SARS-CoV-2
infection,
particularly
in
patients
with
liver
disease.
However,
it
is
uncertain
whether
this
finding
can
be
extended
to
the
allogeneic
hematopoietic
stem
cell
transplantation
(allo-HSCT)
cohort.
Therefore,
we
aim
examine
potential
of
UDCA
infection
recently
received
allo-HSCT
patients.
Methods
During
initial
Omicron
variant
wave
China
(December
2022
February
2023),
conducted
prospective
observational
study
involving
91
hospitalized
who
had
undergone
within
previous
6
months
as
part
National
Longitudinal
Cohort
Hematological
Diseases
(NICHE).
Throughout
hospitalization,
continuously
monitored
status
COVID-19
using
PCR
kits
or
Antigen
Rapid
Tests.
Results
Among
these
patients,
67.0%
(n
=
61)
were
confirmed
contracted
infection.
For
52
evaluated,
23.1%
experienced
severe
critical
clinical
course.
There
was
no
difference
rate
severity
between
group
and
non-UDCA
group.
We
found
only
transplanted
3
ago
demonstrated
higher
risk
compared
those
(Odds
Ratio
[OR]:
3.241,
95%
Confidence
Interval
[CI]:
1.287-8.814,
P
0.016).
But
other
factors,
such
administration
UDCA,
showed
difference.
Notably,
age
≥38
years
old
remained
an
independent
factor
for
course
(OR:
3.664,
CI:
1.129-13.007,
0.035).
Conclusion
The
effectiveness
protecting
newly
recipients
remains
unconfirmed.
Presently,
most
effective
strategy
appears
minimizing
exposure
SARS-CoV-2.
Clinical
trial
registration
https://clinicaltrials.gov/ct2/show/NCT04645199
,
identifier
NCT04645199.
Language: Английский
Stimulation of Potent Humoral and Cellular Immunity via Synthetic Dual-Antigen MVA-Based COVID-19 Vaccine COH04S1 in Cancer Patients Post Hematopoietic Cell Transplantation and Cellular Therapy
Vaccines,
Journal Year:
2023,
Volume and Issue:
11(9), P. 1492 - 1492
Published: Sept. 15, 2023
Hematopoietic
cell
transplantation
(HCT)
and
chimeric
antigen
receptor
(CAR)-T
patients
are
immunocompromised,
remain
at
high
risk
following
SARS-CoV-2
infection,
less
likely
than
immunocompetent
individuals
to
respond
vaccination.
As
part
of
the
safety
lead-in
portion
a
phase
2
clinical
trial
in
post
HCT/CAR-T
for
hematological
malignancies
(HM),
we
tested
immunogenicity
synthetic
modified
vaccinia
Ankara-based
COVID-19
vaccine
COH04S1
co-expressing
spike
(S)
nucleocapsid
(N)
antigens.
Thirteen
were
vaccinated
3-12
months
with
two
four
doses
COH04S1.
antigen-specific
humoral
cellular
immune
responses,
including
neutralizing
antibodies
ancestral
virus
variants
concern
(VOC),
measured
up
six
vaccination
compared
responses
historical
cohorts
naïve
healthy
volunteers
(HV)
healthcare
workers
(HCW)
FDA-approved
mRNA
Comirnaty®
(Pfizer,
New
York,
NY,
USA).
After
one
or
doses,
recipients
showed
significant
increase
S-
N-specific
binding
antibody
titers
potent
activity
against
VOC,
highly
evasive
Omicron
XBB.1.5
variant.
Furthermore,
resulted
T
cells,
predominantly
CD4+
lymphocytes.
Elevated
continued
persist
both
COH04S1-vaccinated
superior
comparable
those
HV
Comirnaty®-vaccinated
HCW.
These
results
demonstrate
robust
stimulation
cross-reactive
by
HM
HCT/CAR-T,
supporting
further
testing
immunocompromised
populations.
Language: Английский
Characteristics and Outcomes of Stem Cell Transplant Patients during the COVID-19 Era: A Systematic Review and Meta-Analysis
Healthcare,
Journal Year:
2024,
Volume and Issue:
12(5), P. 530 - 530
Published: Feb. 23, 2024
This
systematic
review
and
meta-analysis
aims
to
identify
the
outcomes
of
stem
cell
transplant
(SCT)
patients
during
COVID-19
era.
Pooled
event
rates
(PER)
were
calculated,
meta-regression
was
performed.
A
random
effects
model
utilized.
In
total,
36
eligible
studies
included
out
290.
The
PER
COVID-19-related
deaths
hospital
admissions
21.1%
55.2%,
respectively.
use
hydroxychloroquine
53.27%,
receipt
immunosuppression
it
39.4%,
antivirals,
antibiotics,
steroids
71.61%,
37.94%,
18.46%,
time
elapsed
until
infection
after
SCT
more
than
6
months
85.3%.
fever,
respiratory
symptoms,
gastrointestinal
symptoms
70.9,
76.1,
19.3%,
acute
chronic
GvHD
40.2%
60.9%,
are
at
a
higher
risk
severe
mortality.
dexamethasone
improves
survival
hospitalized
with
moderate
requiring
supplemental
oxygen
or
ventilation.
patient
group
is
heterogeneous
varying
characteristics.
quality
reporting
on
these
when
infected
not
uniform
further
prospective
registry
needed
better
guide
clinical
care
in
this
unique
setting.
Language: Английский
COVID-19 antibody titers after tixagevimab–cilgavimab injection in patients with hematologic diseases; a single-center, prospective study
Naokazu Nakamura,
No information about this author
Hiroko Tsunemine,
No information about this author
Ryo Ikunari
No information about this author
et al.
Leukemia & lymphoma/Leukemia and lymphoma,
Journal Year:
2024,
Volume and Issue:
65(8), P. 1117 - 1126
Published: April 16, 2024
Knowledge
of
the
SARS-CoV-2
antibody
titers
induced
by
tixagevimab–cilgavimab
in
patients
with
hematologic
diseases
remains
insufficient.
Here,
we
performed
a
single-center,
prospective
study
to
reveal
changes
titer
after
administration
78
diseases.
The
median
peak
was
155.4
U/mL,
and
AUC
46556
days·U/mL.
First,
compared
several
characteristics
between
low
(peak
≤
U/mL)
high
>
U/mL).
We
extracted
6
factors
(patient
age,
sex,
ECOG-PS,
serum
albumin
level,
cross-sectional
area
computed
tomographic
number
psoas
major
muscle)
as
candidates
influencing
titers.
Multiple
regression
analysis
revealed
that
closely
associated
these
(contribution
rate
=
0.76,
p
0.02).
Our
data
support
inability
induce
sufficient
against
SARS-CoV-2,
especially
older,
frailer,
female
patients.
Language: Английский
Raising awareness may increase the likelihood of hematopoietic stem cell donation: analysis of a nationwide survey using Artificial Intelligence
Research Square (Research Square),
Journal Year:
2024,
Volume and Issue:
unknown
Published: April 26, 2024
Abstract
Background:
In
Italy,
the
demand
for
allogeneic
transplantation
exceeds
number
of
compatible
donors
registered
in
Italian
Bone
Marrow
Donor
Registry
(IBMDR).
As
various
factors
likely
contribute
to
donor
shortage,
our
aim
was
explore
knowledge,
beliefs,
opinions,
values,
and
feelings
population
regarding
stem
cell
donation.
Methods:
An
online
survey
shared
through
social
media.
Two
groups
respondents
were
retrospectively
identified
as
those
who
(currently
or
previously)
on
IBMDR
(Donor
Group)
had
never
(Non-Donor
Group).
Statistical
analyses
performed
confirm
relationship
between
respondents’
knowledge
level
their
willingness
donate.
Then,
a
generative
artificial
intelligence
strategy
applied
using
questionnaire
responses
features
train
6
different
classifiers
machine
learning
process.
The
predict
probability
enrollment.
Results:
A
total
1518
from
throughout
Italy
participated
study.
Among
NDG,
lower
donation
needs
(51.7%
vs
24.4%,
p<0.001)
negative
such
fear
(Z=-2.2642,
p=0.02),
perplexity
(Z=4.4821,
p<0.001),
uncertainty
(Z=3.3425,
emerged.
higher
about
associated
processes
predicted
greater
likelihood
analysis
showed
an
area
under
ROC
curve
(AUC)
ranging
0.65
0.81,
depending
classifier.
Conclusions:
results
underscore
need
improve
strategies
raise
awareness
its
process
among
population.
Language: Английский
Impact of prior COVID‐19 infection on allogeneic hematopoietic stem cell transplantation outcomes
Clinical Transplantation,
Journal Year:
2024,
Volume and Issue:
38(5)
Published: May 1, 2024
Abstract
There
are
limited
data
on
outcomes
of
allogeneic
hematopoietic
stem
cell
transplantation
(allo‐HSCT)
in
recipients
with
prior
COVID‐19
infection.
This
single‐center
retrospective
study
included
54
adult
patients
who
received
allo‐HSCT
from
July
2020
to
September
2021
after
previous
infection
and
122
control
group
without
a
history
underwent
HSCT
during
the
same
period,
median
follow‐up
17
months.
Median
time
was
211
days.
The
incidence
main
complications
post‐transplant
period
not
significantly
different
between
two
groups:
deep
vein
thrombosis
(
p
=
.85),
TMA
.8),
VOD
.25),
bloodstream
infections
.21),
pneumonia
any
etiology
.41),
viral
invasive
fungal
disease
.08).
2‐year
non‐relapse
mortality,
relapse
incidence,
overall
survival,
progression‐free
survival
also
were
comparable
22%
(95%
CI
10.5–36.2)
versus
26.3%
18.7–34.6)
.4;
15.6%
7.3–26.9)
23.6%
16.0–32.3)
.39;
67.9%
50.4–80.3)
59.8%
50.2–68.1)
.24
62.3%
45.5–75.3)
49.9%
40.0–59.1)
.18,
respectively.
did
affect
results
allo‐HSCT.
Language: Английский
Outcomes of hematopoietic stem cell transplantation in patients with SARS-CoV-2 infection during the Omicron era
Won Jun Choi,
No information about this author
Jinhong Lee,
No information about this author
Kowoon Choi
No information about this author
et al.
International Journal of Infectious Diseases,
Journal Year:
2024,
Volume and Issue:
147, P. 107207 - 107207
Published: Aug. 14, 2024
Language: Английский
Immunogenicity of Comirnaty Omicron XBB.1.5 booster COVID-19 mRNA vaccine in long-term survivors after allogeneic hematopoietic stem cell transplantation
Scientific Reports,
Journal Year:
2024,
Volume and Issue:
14(1)
Published: Oct. 21, 2024
Abstract
Primary
mRNA
vaccination
against
COVID-19
typically
involves
three
doses
for
immunocompromised
individuals,
including
hematopoietic
stem
cell
transplantation
(allo-HSCT)
recipients.
However,
optimal
subsequent
boosting
strategies
remain
unclear.
This
study
aimed
to
assess
the
immunogenicity
of
a
booster
dose
using
most
recently
updated
vaccine
(Comirnaty
Omicron
XBB.1.5)
among
long-term
allo-HSCT
survivors
having
previously
received
multiple
doses,
in
median
4
(2–6).
Thirty-four
recipients
were
enrolled
at
Sahlgrenska
University
Hospital,
and
peripheral
blood
samples
collected
immediately
before
four
weeks
after
booster.
Antibodies
receptor-binding
domain
(anti-RBD)
spike
1
(S1)
nucleocapsid,
as
well
S1-specific
ex
vivo
T-cell
responses,
evaluated.
Adverse
events
monitored.
Despite
13
months
since
prior
dose,
both
humoral
responses
S1
present
pre-booster
all
but
two
participants,
who
suffered
from
severe
chronic
Graft-versus-host
disease.
Notably,
62%
participants
had
confirmed
infection.
Significantly
higher
antibody
levels
observed
women
than
men
(
p
=
0.003).
Booster
dosing
strengthened
specific
T
equalized
gender
differences,
although
remained
significantly
lower
those
receiving
immunosuppressive
treatment
0.041).
In
population
survivors,
majority
whom
infection,
pre-
post-booster
immune
robust.
patients
undergoing
GvHD
exhibited
weaker
responses.
Language: Английский
Prevention is better than cure: immunocompromised people need COVID-19 prevention therapies now
Infectious Diseases,
Journal Year:
2024,
Volume and Issue:
56(12), P. 1107 - 1110
Published: Oct. 31, 2024
Immunocompromised
people
are
facing
ongoing
inequality
in
health
outcomes
because
of
COVID-19.
Let's
remain
ambitious
and
improve
availability
access
to
COVID-19
prevention
therapies
that
protect
patients
aid
management.
This
article
brings
together
opinions
from
four
experts
based
the
United
Kingdom
who
specialise
immunology,
solid
organ
transplantation,
respiratory
medicine
critical
care,
oncology
haematology.
In
this
article,
they
communicate
impact
SARS-CoV-2
infection
on
vulnerable
with
underlying
conditions
need
for
immediate
policies
Language: Английский