Frontiers in Immunology,
Journal Year:
2020,
Volume and Issue:
11
Published: Aug. 11, 2020
Evidence
from
the
global
outbreak
of
SARS-CoV-2
has
clearly
demonstrated
that
individuals
with
pre-existing
comorbidities
are
at
a
much
greater
risk
dying
COVID-19.
This
is
great
concern
for
living
these
conditions,
and
major
challenge
healthcare
systems
biomedical
research.
Not
all
confer
same
risk,
however,
many
affect
function
immune
system,
which
in
turn
directly
impacts
response
to
Furthermore,
myriad
drugs
prescribed
can
also
influence
progression
COVID-19
limit
additional
treatment
options
available
Here,
we
review
dysfunction
infection
impact
on
development
We
explore
how
underlying
disease
etiologies
common
therapies
used
treat
conditions
exacerbate
progression.
Moreover,
discuss
long-term
challenges
associated
use
both
novel
repurposed
patients
comorbidities.
Journal of Clinical Oncology,
Journal Year:
2022,
Volume and Issue:
40(13), P. 1474 - 1486
Published: Feb. 4, 2022
PURPOSE
Women
have
more
adverse
events
(AEs)
from
chemotherapy
than
men,
but
few
studies
investigated
sex
differences
in
immune
or
targeted
therapies.
We
examined
AEs
by
across
different
treatment
domains.
METHODS
analyzed
treatment-related
SWOG
phase
II
and
III
clinical
trials
conducted
between
1980
2019,
excluding
sex-specific
cancers.
AE
codes
grade
were
categorized
using
the
Common
Terminology
Criteria
for
Adverse
Events.
Symptomatic
defined
as
those
aligned
with
National
Cancer
Institute's
Patient-Reported
Outcome–Common
Events;
laboratory-based
observable/measurable
designated
objective
(hematologic
v
nonhematologic).
Multivariable
logistic
regression
was
used,
adjusting
age,
race,
disease
prognosis.
Thirteen
symptomatic
14
categories
examined.
RESULTS
In
total,
N
=
23,296
patients
(women,
8,838
[37.9%];
14,458
[62.1%])
202
experiencing
274,688
analyzed;
17,417
received
chemotherapy,
2,319
immunotherapy,
3,560
therapy.
Overall,
64.6%
(n
15,051)
experienced
one
severe
(grade
≥
3)
AEs.
had
a
34%
increased
risk
of
compared
men
(odds
ratio
[OR]
1.34;
95%
CI,
1.27
to
1.42;
P
<
.001),
including
49%
among
receiving
immunotherapy
(OR
1.49;
1.24
1.78;
.001).
an
all
treatments,
especially
1.66;
1.37
2.01;
hematologic
AE.
No
statistically
significant
nonhematologic
found.
CONCLUSION
The
greater
severity
both
women
multiple
modalities
indicates
that
broad-based
exist.
This
could
be
due
reported,
pharmacogenomics
drug
metabolism/disposition,
total
dose
received,
and/or
adherence
Particularly
large
observed
suggesting
studying
these
agents
is
priority.
Annals of the Rheumatic Diseases,
Journal Year:
2021,
Volume and Issue:
80(10), P. 1312 - 1316
Published: May 6, 2021
To
better
understand
the
factors
that
influence
humoral
immune
response
to
vaccination
against
SARS-CoV-2
in
patients
with
immune-mediated
inflammatory
diseases
(IMIDs).Patients
and
controls
from
a
large
COVID-19
study,
(1)
no
previous
history
of
COVID-19,
(2)
negative
baseline
anti-SARS-CoV-2
IgG
test
(3)
at
least
10
days
before
serum
collection
were
measured
for
IgG.
Demographic,
disease-specific
vaccination-specific
data
recorded.Vaccination
responses
84
IMID
182
analysed.
While
all
developed
IgG,
five
failed
develop
(p=0.003).
Moreover,
99.5%
but
only
90.5%
neutralising
antibody
activity
(p=0.0008).
Overall
delayed
reduced
(mean
(SD):
6.47
(3.14))
compared
(9.36
(1.85);
p<0.001).
Estimated
marginal
means
(95%
CI)
adjusted
age,
sex
time
first
sampling
8.48
(8.12-8.85)
6.90
(6.45-7.35)
IMIDs.
Significantly
pertained
untreated,
conventionally
anticytokine
treated
IMID.Immune
are
IMID.
This
effect
is
based
on
disease
itself
rather
than
concomitant
treatment.
Frontiers in Immunology,
Journal Year:
2021,
Volume and Issue:
12
Published: Aug. 31, 2021
The
ongoing
COVID-19
pandemic
has
increased
awareness
about
sex-specific
differences
in
immunity
and
outcomes
following
SARS-CoV-2
infection.
Strong
evidence
of
a
male
bias
disease
severity
is
hypothesized
to
be
mediated
by
sex
differential
immune
responses
against
SARS-CoV-2.
This
hypothesis
based
on
data
from
other
viral
infections,
including
influenza
viruses,
HIV,
hepatitis
others
that
have
demonstrated
infections.
Although
males
are
more
susceptible
most
females
possess
immunological
features
render
them
vulnerable
distinct
immune-related
outcomes.
Both
chromosome
complement
related
genes
as
well
steroids
play
important
roles
mediating
the
development
Frontiers in Immunology,
Journal Year:
2020,
Volume and Issue:
11
Published: Aug. 11, 2020
Evidence
from
the
global
outbreak
of
SARS-CoV-2
has
clearly
demonstrated
that
individuals
with
pre-existing
comorbidities
are
at
a
much
greater
risk
dying
COVID-19.
This
is
great
concern
for
living
these
conditions,
and
major
challenge
healthcare
systems
biomedical
research.
Not
all
confer
same
risk,
however,
many
affect
function
immune
system,
which
in
turn
directly
impacts
response
to
Furthermore,
myriad
drugs
prescribed
can
also
influence
progression
COVID-19
limit
additional
treatment
options
available
Here,
we
review
dysfunction
infection
impact
on
development
We
explore
how
underlying
disease
etiologies
common
therapies
used
treat
conditions
exacerbate
progression.
Moreover,
discuss
long-term
challenges
associated
use
both
novel
repurposed
patients
comorbidities.