Mycopathologia,
Journal Year:
2023,
Volume and Issue:
188(5), P. 667 - 681
Published: April 26, 2023
Abstract
Despite
improvements
in
treatment
and
diagnostics
over
the
last
two
decades,
invasive
aspergillosis
(IA)
remains
a
devastating
fungal
disease.
The
number
of
immunocompromised
patients
hence
vulnerable
hosts
increases,
which
is
paralleled
by
emergence
rise
IA
cases.
Increased
frequencies
azole-resistant
strains
are
reported
from
six
continents,
presenting
new
challenge
for
therapeutic
management.
Treatment
options
currently
consist
three
classes
antifungals
(azoles,
polyenes,
echinocandins)
with
distinctive
advantages
shortcomings.
Especially
settings
difficult
to
treat
IA,
comprising
drug
tolerance/resistance,
limiting
drug–drug
interactions,
and/or
severe
underlying
organ
dysfunction,
novel
approaches
urgently
needed.
Promising
drugs
late-stage
clinical
development,
including
olorofim
(a
dihydroorotate
dehydrogenase
inhibitor),
fosmanogepix
Gwt1
enzyme
ibrexafungerp
triterpenoid),
opelconazole
(an
azole
optimized
inhalation)
rezafungin
echinocandin
long
half-life
time).
Further,
insights
pathophysiology
yielding
immunotherapy
as
potential
add-on
therapy.
Current
investigations
show
encouraging
results,
so
far
mostly
preclinical
settings.
In
this
review
we
discuss
current
strategies,
give
an
outlook
on
possible
pharmaceutical
options,
and,
lastly,
provide
overview
ongoing
research
IA.
Journal of Clinical Microbiology,
Journal Year:
2023,
Volume and Issue:
61(3)
Published: Feb. 21, 2023
Timely
diagnosis
remains
an
unmet
need
in
non-neutropenic
patients
at
risk
for
aspergillosis,
including
those
with
COVID-19-associated
pulmonary
aspergillosis
(CAPA),
which
its
early
stages
is
characterized
by
tissue-invasive
growth
of
the
lungs
limited
angioinvasion.
Currently
available
mycological
tests
show
sensitivity
when
testing
blood
specimens.
BMC Infectious Diseases,
Journal Year:
2023,
Volume and Issue:
23(1)
Published: April 18, 2023
Critically
ill
COVID-19
patients
are
highly
susceptible
to
opportunistic
fungal
infection
due
many
factors,
including
virus-induced
immune
dysregulation,
host-related
comorbidities,
overuse
and
misuse
of
antibiotics
or
corticosteroids,
modulator
drugs,
the
emergencies
caused
by
pandemic.
This
study
aimed
assess
incidence,
identify
potential
risk
examine
impact
coinfection
on
outcomes
admitted
intensive
care
unit
(ICU).A
prospective
cohort
253
critically
aged
18
years
older
isolation
ICU
Zagazig
University
Hospitals
over
a
4-month
period
from
May
2021
August
was
conducted.
The
detection
carried
out.Eighty-three
(83)
(32.8%)
were
diagnosed
with
coinfection.
Candida
most
frequently
isolated
fungus
in
61
(24.1%)
patients,
followed
molds,
which
included
Aspergillus
11
(4.3%)
mucormycosis
five
(1.97%),
six
(2.4%)
other
rare
fungi.
Poor
diabetic
control,
prolonged
high-dose
steroids,
multiple
comorbidities
all
possible
factors
for
[OR
(95%
CI)
=
10.21
(3.43-30.39),
14.1
(5.67-35.10),
14.57
(5.83-33.78),
4.57
(1.83-14.88),
respectively].Fungal
is
common
complication
ICU.
Candidiasis,
aspergillosis,
COVID-19-associated
infections
have
great
mortality
rates.
PLoS Pathogens,
Journal Year:
2023,
Volume and Issue:
19(5), P. e1011322 - e1011322
Published: May 4, 2023
With
over
300
million
severe
cases
and
1.5
deaths
annually,
invasive
fungal
diseases
(IFDs)
are
a
major
medical
burden
source
of
global
morbidity
mortality.
The
World
Health
Organization
(WHO)
recently
released
the
first-ever
priority
pathogens
list
including
19
pathogens,
considering
perceived
public
health
importance.
Most
pathogenic
fungi
opportunistic
cause
in
patients
under
immunocompromised
conditions
such
as
HIV
infection,
cancer,
chemotherapy,
transplantation,
immune
suppressive
drug
therapy.
Worryingly,
mortality
caused
by
IFDs
continuously
on
rise
due
to
limited
available
antifungal
therapies,
emergence
resistance,
increase
population
that
is
vulnerable
IFDs.
Moreover,
COVID-19
pandemic
worsened
globe
threat
it
predisposes
secondary
life-threatening
fungi.
In
this
mini-review,
we
provide
perspective
advances
strategies
for
combating
with
therapies.
PLoS Pathogens,
Journal Year:
2023,
Volume and Issue:
19(1), P. e1011025 - e1011025
Published: Jan. 5, 2023
Racial
and
ethnic
identities,
largely
understood
as
social
rather
than
biologic
constructs,
may
impact
risk
for
acquiring
infectious
diseases,
including
fungal
infections.
Risk
factors
include
genetic
immunologic
differences
such
aberrations
in
host
immune
response,
polymorphisms,
epigenomic
stemming
from
environmental
exposures
underlying
determinants
of
health.
In
addition,
certain
racial
groups
be
predisposed
to
diseases
that
increase
infections,
well
disparities
healthcare
access
health
insurance.
this
review,
we
analyzed
identities
race
ethnicity
they
relate
severe
disease
invasive
mold
infections
aspergillosis
appear
related
health,
although
polymorphisms
contribute
some
circumstances.
Although
black
African
American
individuals
at
high
superficial
Candida
cryptococcosis,
the
reasons
are
unclear
underling
healthcare,
other
socioeconomic
disparities.
all
endemic
fungi
likely
socioeconomic,
disparities,
mechanisms
play
a
role
well,
particularly
disseminated
coccidioidomycosis.
Mycopathologia,
Journal Year:
2023,
Volume and Issue:
188(5), P. 667 - 681
Published: April 26, 2023
Abstract
Despite
improvements
in
treatment
and
diagnostics
over
the
last
two
decades,
invasive
aspergillosis
(IA)
remains
a
devastating
fungal
disease.
The
number
of
immunocompromised
patients
hence
vulnerable
hosts
increases,
which
is
paralleled
by
emergence
rise
IA
cases.
Increased
frequencies
azole-resistant
strains
are
reported
from
six
continents,
presenting
new
challenge
for
therapeutic
management.
Treatment
options
currently
consist
three
classes
antifungals
(azoles,
polyenes,
echinocandins)
with
distinctive
advantages
shortcomings.
Especially
settings
difficult
to
treat
IA,
comprising
drug
tolerance/resistance,
limiting
drug–drug
interactions,
and/or
severe
underlying
organ
dysfunction,
novel
approaches
urgently
needed.
Promising
drugs
late-stage
clinical
development,
including
olorofim
(a
dihydroorotate
dehydrogenase
inhibitor),
fosmanogepix
Gwt1
enzyme
ibrexafungerp
triterpenoid),
opelconazole
(an
azole
optimized
inhalation)
rezafungin
echinocandin
long
half-life
time).
Further,
insights
pathophysiology
yielding
immunotherapy
as
potential
add-on
therapy.
Current
investigations
show
encouraging
results,
so
far
mostly
preclinical
settings.
In
this
review
we
discuss
current
strategies,
give
an
outlook
on
possible
pharmaceutical
options,
and,
lastly,
provide
overview
ongoing
research
IA.