Biomedicines,
Journal Year:
2023,
Volume and Issue:
11(2), P. 617 - 617
Published: Feb. 18, 2023
Antiretrovirals
(ARVs)
reduce
Human
Immunodeficiency
Virus
(HIV)
loads
to
undetectable
levels
in
infected
patients.
However,
HIV
can
persist
throughout
the
body
cellular
reservoirs
partly
due
inability
of
some
ARVs
cross
anatomical
barriers
and
capacity
HIV-1
establish
latent
infection
resting
CD4+
T
cells
monocytes/macrophages.
A
cure
for
is
not
likely
unless
latency
addressed
delivery
reservoir
sites
improved.
Nanomedicine
has
been
used
ARV
formulations
improve
efficacy.
More
specifically,
researchers
are
exploring
benefit
using
nanoparticles
nanomedicine
eradication
strategies
such
as
shock
kill,
block
lock,
others.
This
review
will
focus
on
mechanisms
nanomedicine-based
approaches
treat
HIV.
Viruses,
Journal Year:
2022,
Volume and Issue:
14(4), P. 829 - 829
Published: April 16, 2022
The
achievement
of
an
HIV
cure
is
dependent
on
the
eradication
or
permanent
silencing
HIV-latent
viral
reservoirs,
including
understudied
central
nervous
system
(CNS)
reservoir.
This
requires
a
deep
understanding
molecular
mechanisms
HIV's
entry
into
CNS,
latency
establishment,
persistence,
and
reversal.
Therefore,
representative
CNS
culture
models
that
reflect
intercellular
dynamics
pathophysiology
human
brain
are
urgently
needed
in
order
to
study
reservoir
HIV-induced
neuropathogenesis.
In
this
study,
we
characterized
cerebral
organoid
model
which
microglia
grow
intrinsically
as
infection
CNS.
We
demonstrated
both
organoids
isolated
organoid-derived
(oMG),
infected
with
replication-competent
HIVbal
reporter
viruses,
support
productive
via
CCR5
co-receptor.
Productive
was
only
observed
microglial
cells.
Fluorescence
analysis
revealed
target
cell.
Susceptibility
co-expression
microglia-specific
markers
CD4
receptors.
Altogether,
will
be
valuable
tool
within
research
community
HIV-CNS
interactions,
underlying
HIV-associated
neurological
disorders
(HAND),
efficacy
new
therapeutic
curative
strategies
Retrovirology,
Journal Year:
2023,
Volume and Issue:
20(1)
Published: Jan. 13, 2023
Abstract
HIV-associated
neurological
disorders
(HAND)
affect
up
to
50%
of
people
living
with
HIV
(PLWH),
even
in
the
era
combination
antiretroviral
therapy
(cART).
HIV-DNA
can
be
detected
cerebral
spinal
fluid
(CSF)
approximately
half
aviremic
ART-suppressed
PLWH
and
its
presence
is
associated
poorer
neurocognitive
performance.
DNA
+
RNA
cells
have
also
been
observed
postmortem
brain
tissue
individuals
sustained
cART
suppression.
In
this
review,
we
provide
an
overview
how
invades
infection
resident
glial
(astrocytes
microglia).
We
discuss
role
persistent
neuroinflammation
HAND
their
potential
contribution
reservoir.
eradication
strategies
that
target
persistently
infected
glia
will
likely
needed
achieve
cure.
International Journal of Molecular Sciences,
Journal Year:
2023,
Volume and Issue:
24(4), P. 3514 - 3514
Published: Feb. 9, 2023
Neuroinfections
of
the
central
nervous
system
(CNS)
can
be
triggered
by
various
pathogens.
Viruses
are
most
widespread
and
have
potential
to
induce
long-term
neurologic
symptoms
with
potentially
lethal
outcomes.
In
addition
directly
affecting
their
host
cells
inducing
immediate
changes
in
a
plethora
cellular
processes,
viral
infections
CNS
also
trigger
an
intense
immune
response.
Regulation
innate
response
depends
not
only
on
microglia,
which
fundamental
CNS,
but
astrocytes.
These
align
blood
vessels
ventricle
cavities,
consequently,
they
one
first
cell
types
become
infected
after
virus
breaches
CNS.
Moreover,
astrocytes
increasingly
recognized
as
reservoir
CNS;
therefore,
initiated
presence
intracellular
particles
may
profound
effect
tissue
physiology
morphology.
should
addressed
terms
persisting
because
contribute
recurring
sequelae.
To
date,
different
viruses
originating
from
genetically
distinct
families,
including
Flaviviridae,
Coronaviridae,
Retroviridae,
Togaviridae,
Paramyxoviridae,
Picomaviridae,
Rhabdoviridae,
Herpesviridae,
been
confirmed.
Astrocytes
express
receptors
that
detect
signaling
cascades,
leading
this
review,
we
summarize
current
knowledge
initiate
release
inflammatory
cytokines
depict
involvement
functions
Journal of Neuroinflammation,
Journal Year:
2025,
Volume and Issue:
22(1)
Published: March 5, 2025
HIV-1-associated
neurocognitive
impairment
(HIV-1-NCI)
is
marked
by
ongoing
and
chronic
neuroinflammation
with
loss
decline
in
neuronal
function
even
when
antiretroviral
drug
therapy
(ART)
successfully
suppresses
viral
replication.
Microglia,
the
primary
reservoirs
of
HIV-1
central
nervous
system
(CNS),
play
a
significant
role
maintaining
this
neuroinflammatory
state.
However,
understanding
how
generated
sustained
HIV-1,
or
impacted
ART,
difficult
due
to
limited
access
human
CNS
tissue.
We
an
vitro
model
admixed
hematopoietic
progenitor
cell
(HPC)
derived
microglia
embedded
into
embryonic
stem
(ESC)
Brain
Organoids
(BO).
Microglia
were
infected
prior
co-culture.
Infected
co-cultured
brain
organoids
BOs
infiltrate
establish
for
infection,
"HIV-1
M-BO".
M-BOs
treated
ART
variable
directions.
infection
was
monitored
p24
ELISA
digital
droplet
PCR
(ddPCR).
Inflammation
measured
cytokine
p-NF-kB
levels
using
multiplex
ELISA,
flow
cytometry
confocal
microscopy.
could
be
create
"brain"
infection.
Although
initial
source
pro-inflammatory
cytokines,
astrocytes,
neurons
neural
cells
also
had
increased
levels,
along
elevated
CCL2
supernatant
compared
Uninfected
M-BOs.
suppressed
virus
below
limit
detection
but
did
not
decrease
neuroinflammation.
These
findings
indicate
that
are
pro-inflammatory.
significantly
inflammation
persisted
ART-treated
Together,
these
infiltrated
provides
robust
understand
impact
on
Frontiers in Immunology,
Journal Year:
2021,
Volume and Issue:
12
Published: Oct. 4, 2021
Severe
acute
respiratory
syndrome
coronavirus
2
(SARS-CoV-2)
is
a
major
public
health
issue.
COVID-19
considered
an
airway/multi-systemic
disease,
and
demise
has
been
associated
with
uncontrolled
immune
response
cytokine
storm
in
to
the
virus.
However,
lung
pathology,
response,
tissue
damage
are
poorly
described
understood
due
safety
concerns.
Using
post-mortem
tissues
from
uninfected
deadly
cases
as
well
unbiased
combined
analysis
of
histology,
multi-viral
host
markers
staining,
correlative
microscopy,
confocal,
image
analysis,
we
identified
three
distinct
phenotypes
COVID-19-induced
damage.
First,
hemorrhage
characterized
by
minimal
infiltration
large
thrombus;
Second,
excessive
cell
but
no
hemorrhagic
events.
The
third
phenotype
correspond
combination
two
previous
ones.
We
observed
loss
alveolar
wall
integrity,
detachment
pieces,
fibroblast
proliferation,
extensive
fibrosis
all
phenotypes.
Although
studied
were
lethal
COVID-19,
strong
was
analyzed
significant
B
poor
T
infiltrations,
suggesting
exhausted
or
compromised
cellular
these
patients.
Overall,
our
data
show
that
SARS-CoV-2-induced
highly
heterogeneous.
These
individual
differences
need
be
understand
long-term
consequences.
Cells,
Journal Year:
2022,
Volume and Issue:
11(15), P. 2379 - 2379
Published: Aug. 2, 2022
The
major
barrier
to
cure
HIV
infection
is
the
early
generation
and
extended
survival
of
reservoirs
in
circulation
tissues.
Currently,
techniques
used
detect
quantify
are
mostly
based
on
blood-based
assays;
however,
it
has
become
evident
that
viral
remain
Our
study
describes
a
novel
multi-component
imaging
method
(HIV
DNA,
mRNA,
proteins
same
assay)
identify,
quantify,
characterize
tissues
blood
products
obtained
from
HIV-infected
individuals
even
when
systemic
replication
undetectable.
In
human
brains
under
ART,
we
identified
microglia/macrophages
small
population
astrocytes
main
cells
with
integrated
DNA.
Only
half
DNA
expressed
one-third
proteins.
Surprisingly,
residual
HIV-p24,
gp120,
nef,
vpr,
tat
protein
expression
accumulation
uninfected
around
suggesting
local
synthesis,
secretion,
bystander
uptake.
conclusion,
our
data
show
ART
reduces
size
brain’s
reservoirs;
local/chronic
secretion
still
occurs,
indicating
brain
anatomical
target
infection.
Cell Reports,
Journal Year:
2023,
Volume and Issue:
42(9), P. 113053 - 113053
Published: Sept. 1, 2023
HIV
persists
in
tissues
during
antiretroviral
therapy
(ART),
but
the
relative
contribution
of
different
anatomical
compartments
to
viral
reservoir
humans
remains
unknown.
We
performed
an
extensive
characterization
reservoirs
two
men
who
donated
their
bodies
cure
research
and
had
been
on
suppressive
ART
for
years.
DNA
is
detected
all
tissues,
with
large
variations
across
between
participants.
Intact
genomes
represent
2%
25%
proviruses
participants
are
mainly
secondary
lymphoid
organs,
spleen
mediastinal
lymph
nodes
harboring
intact
both
individuals.
Multiple
copies
identical
found
indicating
that
clonal
expansions
common
sites.
The
majority
(>85%)
these
expanded
clones
shared
multiple
tissues.
These
findings
suggest
infected
cells
expand,
migrate,
possibly
circulate
Advanced Science,
Journal Year:
2024,
Volume and Issue:
11(23)
Published: April 4, 2024
Abstract
Delivering
cargo
to
the
central
nervous
system
(CNS)
remains
a
pharmacological
challenge.
For
infectious
diseases
such
as
HIV,
CNS
acts
latent
reservoir
that
is
inadequately
managed
by
systemic
antiretrovirals
(ARTs).
ARTs
thus
cannot
eradicate
and
given
infection,
patients
experience
neurological
deficits
collectively
referred
“neuroHIV”.
Herein,
development
of
bioinspired
ionic
liquid‐coated
nanoparticles
(IL‐NPs)
for
in
situ
hitchhiking
on
red
blood
cells
(RBCs)
reported,
which
enables
48%
brain
delivery
intracarotid
arterial‐
infused
cargo.
Moreover,
IL
choline
trans‐2‐hexenoate
(CA2HA
1:2)
demonstrates
preferential
accumulation
parenchymal
microglia
over
endothelial
post‐delivery.
This
study
further
successful
loading
abacavir
(ABC),
an
ART
challenging
encapsulate,
into
IL‐NPs,
verifies
retention
antiviral
efficacy
vitro.
IL‐NPs
are
not
cytotoxic
primary
human
peripheral
mononuclear
(PBMCs)
CA2HA
1:2
coating
itself
confers
notable
anti‐viremic
capacity.
In
addition,
vitro
cell
culture
assays
show
markedly
increased
uptake
neural
compared
bare
PLGA
nanoparticles.
work
debuts
liquids
promising
nanoparticle
coatings
assist
biodistribution
has
potential
revolutionize
cargos
(i.e.,
drugs,
viral
vectors)
through
compartmental
barriers
blood‐brain‐barrier
(BBB).
Pathogens,
Journal Year:
2023,
Volume and Issue:
12(7), P. 879 - 879
Published: June 27, 2023
A
major
roadblock
to
achieving
a
cure
for
human
immunodeficiency
virus
type
one
(HIV-1)
is
the
persistence
of
latent
viral
infections
in
cells
and
tissue
compartments
an
infected
host.
Latent
HIV-1
proviral
DNA
persists
resting
memory
CD4+
T
mononuclear
phagocytes
(MPs;
macrophages,
microglia,
dendritic
cells).
Tissue
reservoirs
both
cell
types
reside
gut,
lymph
nodes,
bone
marrow,
spleen,
liver,
kidney,
skin,
adipose
tissue,
reproductive
organs,
brain.
However,
despite
identification
virus-susceptible
cells,
several
limitations
persist
identifying
broad
persons.
The
include
their
relatively
low
abundance,
precise
latently
lack
biomarkers
cells.
While
primary
MP
transformed
lines
are
used
interrogate
mechanisms
persistence,
they
often
fail
accurately
reflect
host
environments
that
carry
infections.
Given
specificity
HIV-1,
there
few
animal
models
replicate
natural
course
infection
with
any
precision.
These
needs
underlie
importance
humanized
mouse
as
valuable
cost-effective
tools
studying
latency
subsequently
means
eliminating
it.
In
this
review,
we
discuss
advantages
mice
studies
eye
toward
using
these
test
antiretroviral
excision
therapeutics.
goals
research
use
address
how
under
which
circumstances
can
be
detected
eliminated.
Targeting
ultimate
task
at
hand.