Viruses,
Journal Year:
2024,
Volume and Issue:
16(8), P. 1294 - 1294
Published: Aug. 14, 2024
The
acquisition
or
reactivation
of
Epstein–Barr
virus
(EBV)
after
allogeneic
Hematopoietic
Stem
Cell
Transplant
(HSCT)
can
be
associated
with
complications
including
the
development
post-transplant
lymphoproliferative
disorder
(PTLD),
which
is
significant
morbidity
and
mortality.
A
number
risk
factors
for
PTLD
have
been
defined,
T-cell
depletion,
approaches
to
monitoring
EBV,
especially
in
high-risk
patients,
use
preemptive
therapy
upon
viral
activation
described.
Newer
therapies
preemption
treatment
PTLD,
such
as
EBV-specific
cytotoxic
T-cells,
hold
promise.
Further
studies
help
define
risks,
diagnosis,
EBV-related
are
needed
this
at-risk
population.
Frontiers in Immunology,
Journal Year:
2023,
Volume and Issue:
14
Published: July 24, 2023
Compelling
evidence
indicates
that
Epstein
Barr
virus
(EBV)
infection
is
a
prerequisite
for
multiple
sclerosis
(MS).
The
disease
may
arise
from
complex
interplay
between
latent
EBV
infection,
genetic
predisposition,
and
various
environmental
lifestyle
factors
negatively
affect
immune
control
of
the
infection.
Evidence
gene-environment
interactions
epigenetic
modifications
triggered
by
in
genetically
susceptible
individuals
supports
this
view.
This
review
gives
short
introduction
to
host
immunity
discusses
indicating
as
MS.
role
risk
factors,
their
interactions,
MS
pathogenesis
reviewed
put
context
Finally,
possible
preventive
measures
are
discussed
based
on
findings
presented.
Cancers,
Journal Year:
2024,
Volume and Issue:
16(5), P. 991 - 991
Published: Feb. 29, 2024
The
Epstein-Barr
Virus
(EBV)
is
a
double-stranded
DNA-based
human
tumor
virus
that
was
first
isolated
in
1964
from
lymphoma
biopsies.
Since
its
initial
discovery,
EBV
has
been
identified
as
major
contributor
to
numerous
cancers
and
chronic
autoimmune
disorders.
particularly
efficient
at
infecting
B-cells
but
can
also
infect
epithelial
cells,
utilizing
an
array
of
epigenetic
strategies
establish
long-term
latent
infection.
association
with
histone
modifications,
alteration
DNA
methylation
patterns
host
viral
genomes,
microRNA
targeting
cell
factors
are
core
drive
interactions
between
virus,
which
necessary
for
persistence
progression
EBV-associated
diseases.
Therefore,
understanding
regulation
role
post-entry
dynamics
elusive
area
research.
Here,
we
present
current
outlooks
it
pertains
during
infection
propensity
induce
tumorigenesis.
We
review
the
important
regulators
latency
explore
how
involved
differential
profiles
host-virus
cancers.
Journal of Virology,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 17, 2025
Discovered
in
1994
lesions
of
an
AIDS
patient,
Kaposi's
sarcoma-associated
herpesvirus
(KSHV)
is
a
member
the
gammaherpesvirus
subfamily
Herpesviridae
family,
which
contains
total
nine
that
infect
humans.
These
viruses
all
contain
large
envelope
glycoprotein,
glycoprotein
B
(gB),
required
for
viral
fusion
with
host
cell
membrane
to
initial
infection.
Although
atomic
structures
five
other
human
herpesviruses
their
postfusion
conformation
and
one
its
prefusion
are
known,
structure
KSHV
gB
has
not
been
reported.
Here,
we
report
first
ectodomain
determined
by
single-particle
cryogenic
electron
microscopy
(cryoEM).
Despite
similar
global
fold
between
gB,
possesses
local
differences
shared
relatives
herpesviruses.
The
glycosylation
sites
arranged
belts
down
symmetry
axis
distinct
localization
compared
herpesviruses,
occludes
certain
antibody
binding
sites.
An
extended
glycan
chain
observed
domain
I
(DI),
located
proximal
membrane,
may
suggest
possible
role
attachment.
Local
flexibility
IV
(DIV)
governed
molecular
hinges
at
interdomain
junctions
identifies
means
enabling
conformational
change.
A
mutation
III
(DIII)
central
helix
disrupts
incorporation
into
virions
despite
adoption
canonical
vitro.
Taken
together,
this
study
reveals
mechanisms
structural
variability
protein
informs
folding
immunogenicity.IMPORTANCEIn
1994,
cancer-causing
virus
was
discovered
patients,
later
named
(KSHV).
As
latest
herpesvirus,
classified
Herpesviridae.
In
study,
have
expressed
employed
(cryoEM)
determine
structure.
Importantly,
our
resolves
some
glycans
beyond
sugar
moiety.
pattern
unique
KSHV,
impacts
antigenicity
gB.
Our
also
caused
domains
provide
clues
mechanism
behind
drastic
change
states.
Infection Genetics and Evolution,
Journal Year:
2023,
Volume and Issue:
112, P. 105443 - 105443
Published: May 17, 2023
Epstein–Barr
virus
(EBV)
infection
is
extremely
common
worldwide,
with
approximately
90%
of
adults
testing
positive
for
EBV
antibodies.
Human
are
susceptible
to
infection,
and
primary
typically
occurs
early
in
life.
can
cause
infectious
mononucleosis
(IM)
as
well
some
severe
non-neoplastic
diseases,
such
chronic
active
(CAEBV)
EBV-associated
hemophagocytic
lymphohistiocytosis
(EBV-HLH),
which
have
a
heavy
disease
burden.
After
individuals
develop
robust
EBV-specific
T
cell
immune
responses,
CD8+
part
CD4+
cells
functioning
cytotoxic
cells,
defending
against
virus.
Different
proteins
expressed
during
EBV's
lytic
replication
latent
proliferation
varying
degrees
cellular
responses.
Strong
immunity
plays
key
role
controlling
by
decreasing
viral
load
eliminating
infected
cells.
However,
the
persists
healthy
carriers
even
response.
When
reactivated,
it
undergoes
then
transmits
virions
new
host.
Currently,
relationship
between
pathogenesis
lymphoproliferative
diseases
adaptive
system
still
not
fully
clarified
needs
be
explored
future.
Investigating
responses
evoked
utilizing
this
knowledge
design
promising
prophylactic
vaccines
urgent
issues
future
research
due
importance
immunity.
Nature Communications,
Journal Year:
2024,
Volume and Issue:
15(1)
Published: June 21, 2024
Abstract
Epstein-Barr
virus
(EBV)
infects
more
than
95%
of
adults
worldwide
and
is
closely
associated
with
various
malignancies.
Considering
the
complex
life
cycle
EBV,
developing
vaccines
targeting
key
entry
glycoproteins
to
elicit
robust
durable
adaptive
immune
responses
may
provide
better
protection.
EBV
gHgL-,
gB-
gp42-specific
antibodies
in
healthy
carriers
contributed
sera
neutralizing
abilities
vitro,
indicating
that
they
are
potential
antigen
candidates.
To
enhance
immunogenicity
these
antigens,
we
formulate
three
nanovaccines
by
co-delivering
molecular
adjuvants
(CpG
MPLA)
antigens
(gHgL,
gB
or
gp42).
These
induce
humoral
cellular
through
efficient
activation
dendritic
cells
germinal
center
response.
Importantly,
generate
high
levels
recognizing
vulnerable
sites
all
antigens.
IgGs
induced
a
cocktail
vaccine
containing
confer
superior
protection
from
lethal
challenge
female
humanized
mice
compared
IgG
elicited
individual
NP-gHgL,
NP-gB
NP-gp42.
serum
nanovaccine
immunization
against
EBV-associated
lymphoma.
Overall,
shows
promising
candidate
for
further
clinical
trials.
Diagnostics,
Journal Year:
2023,
Volume and Issue:
13(12), P. 2068 - 2068
Published: June 15, 2023
Burkitt
lymphoma
(BL)
is
a
form
of
B-cell
malignancy
that
progresses
aggressively
and
most
often
seen
in
children.
While
Epstein-Barr
virus
(EBV)
double-stranded
DNA
has
been
linked
to
variety
cancers,
it
can
transform
B
lymphocytes
into
immortalized
cells,
as
shown
BL.
Therefore,
the
estimated
prevalence
EBV
population
may
assist
prediction
whether
this
high
risk
increased
BL
cases.
This
systematic
review
meta-analysis
aimed
estimate
patients
with
lymphoma.
Using
appropriate
keywords,
four
electronic
databases
were
searched.
The
quality
included
studies
was
assessed
using
Joanna
Briggs
Institute's
critical
appraisal
tool.
results
reported
percentages
95%
confidence
interval
random-effects
model
(CI).
PROSPERO
used
register
protocol
(CRD42022372293),
135
included.
57.5%
(95%
CI:
51.5
63.4,
n
=
4837).
sensitivity
analyses
demonstrated
consistent
results,
65.2%
quality.
Egger's
test
revealed
there
significant
publication
bias.
found
significantly
proportion
(more
than
50%
patients).
study
recommends
testing
an
alternative
for
predictions
assessment
clinical
disease
status
Viruses,
Journal Year:
2024,
Volume and Issue:
16(9), P. 1357 - 1357
Published: Aug. 25, 2024
Despite
the
introduction
of
Pap
testing
for
screening
to
prevent
cervical
cancer
in
mid-20th
century,
remains
a
common
cause
cancer-related
mortality
and
morbidity
globally.
This
is
primarily
due
differences
access
care
between
low-income
high-income
resource
settings,
resulting
being
one
cancers
with
greatest
health
disparity.
The
discovery
human
papillomavirus
(HPV)
as
near-obligate
viral
can
revolutionize
how
it
be
prevented:
HPV
vaccination
against
infection
prophylaxis
testing-based
detection
treatment
pre-cancers
interception.
As
result
this
progress,
World
Health
Organization
has
championed
elimination
global
problem.
However,
unless
research,
investments,
actions
are
taken
ensure
equitable
these
highly
effective
preventive
interventions,
there
real
threat
exacerbating
current
inequities
cancer.
In
review,
progress
date
challenges
opportunities
fulfilling
potential
HPV-targeted
prevention
control
discussed.