Journal of Biomedical Science,
Journal Year:
2024,
Volume and Issue:
31(1)
Published: Jan. 12, 2024
Abstract
The
developments
of
antibodies
for
cancer
therapeutics
have
made
remarkable
success
in
recent
years.
There
are
multiple
factors
contributing
to
the
biological
molecule
including
origin
antibody,
isotype,
affinity,
avidity
and
mechanism
action.
With
better
understanding
progression
immune
manipulation,
recombinant
formats
used
develop
therapeutic
modalities
manipulating
cells
patients
by
targeting
specific
molecules
control
disease.
These
been
successful
minimizing
side
effects
instead
caused
small
or
systemic
chemotherapy
but
because
developing
resistance
against
these
antibodies,
combination
therapy
is
thought
be
best
bet
patient
care.
Here,
this
review,
we
discussed
different
aspects
affecting
their
efficacy
with
some
relevant
examples
most
studied
approved
US
FDA.
Molecular Biomedicine,
Journal Year:
2024,
Volume and Issue:
5(1)
Published: July 4, 2024
Abstract
Multiple
myeloma
(MM)
is
the
second
most
common
hematological
malignancy
of
plasma
cells,
characterized
by
osteolytic
bone
lesions,
anemia,
hypercalcemia,
renal
failure,
and
accumulation
malignant
cells.
The
pathogenesis
MM
involves
interaction
between
cells
marrow
microenvironment
through
soluble
cytokines
cell
adhesion
molecules,
which
activate
various
signaling
pathways
such
as
PI3K/AKT/mTOR,
RAS/MAPK,
JAK/STAT,
Wnt/β-catenin,
NF-κB
pathways.
Aberrant
activation
these
contributes
to
proliferation,
survival,
migration,
drug
resistance
making
them
attractive
targets
for
therapeutic
intervention.
Currently,
approved
drugs
targeting
in
are
limited,
with
many
inhibitors
inducers
still
preclinical
or
clinical
research
stages.
Therapeutic
options
include
non-targeted
like
alkylating
agents,
corticosteroids,
immunomodulatory
drugs,
proteasome
inhibitors,
histone
deacetylase
inhibitors.
Additionally,
targeted
monoclonal
antibodies,
chimeric
antigen
receptor
T
bispecific
T-cell
engagers,
antibodies
being
used
treatment.
Despite
significant
advancements
treatment,
disease
remains
incurable,
emphasizing
need
development
novel
combined
therapies
based
on
emerging
theoretical
knowledge,
technologies,
platforms.
In
this
review,
we
highlight
key
role
progression
treatment
MM,
exploring
advances
therapy
potential
treatments
offer
further
insights
improving
management
outcomes.
European Journal of Heart Failure,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 10, 2025
Clonal
haematopoiesis
(CH)
is
recognized
as
a
significant
risk
factor
for
various
non-haematologic
conditions,
including
cardiovascular
diseases.
However,
recent
studies
examining
its
relationship
with
heart
failure
(HF)
have
reported
conflicting
findings.
To
address
these
inconsistencies,
the
present
meta-analysis
aimed
to
evaluate
association
of
CH
incidence
and
clinical
outcomes
HF.
MEDLINE,
Cochrane
Library
Scopus
were
searched
until
12
December
2024.
Triple-independent
study
selection,
data
extraction
quality
assessment
performed.
Evidence
was
pooled
using
three-level
mixed-effects
meta-analyses.
Participants
(n
=
57
755)
had
significantly
greater
new-onset
HF
compared
non-CH
group
(hazard
ratio
[HR]
1.23,
95%
confidence
interval
[CI]
1.12-1.35,
p
<
0.0001;
I2
0%),
irrespective
prior
history
coronary
artery
disease.
also
correlated
higher
composite
outcome
all-cause
mortality
hospitalization
(HHF)
in
patients
established
(HR
1.84,
CI
1.25-2.70,
0.002;
0%).
Specifically,
associated
1.95,
1.54-2.47,
3%
increase
every
1%
variant
allele
fraction.
concomitant
56%
HHF
1.56,
1.05-2.33,
0.029;
19%).
an
increased
incident
worse
prognosis
individuals
affected
by
These
findings
highlight
potential
contribute
deeper
understanding
HF,
improve
stratification,
support
more
personalized
approaches
management.
Molecular Therapy,
Journal Year:
2022,
Volume and Issue:
30(8), P. 2800 - 2816
Published: May 6, 2022
Several
preclinical
studies
demonstrate
that
antitumor
efficacy
of
programmed
cell
death-1
(PD-1)/programmed
death-ligand
1
(PD-L1)
blockade
can
be
improved
by
combination
with
other
checkpoint
inhibitors.
Lymphocyte-activation
gene
3
(LAG-3)
is
an
inhibitory
receptor
involved
in
T
exhaustion
and
tumor
immune
escape.
Here,
we
describe
ABL501,
a
bispecific
antibody
targeting
LAG-3
PD-L1
modulating
responses
against
tumors.
ABL501
efficiently
inhibits
both
pathways
enhances
the
activation
effector
CD4
Cancer Immunology Research,
Journal Year:
2022,
Volume and Issue:
10(12), P. 1423 - 1432
Published: Oct. 20, 2022
The
sialic
acid-binding
immunoglobulin-like
lectin
(Siglec)-sialic
acid
immune
axis
is
an
evolutionarily
conserved
immunoregulatory
pathway
that
provides
a
mechanism
for
establishing
self-recognition
and
combatting
invasive
pathogens.
Perturbations
in
the
lead
to
many
dysregulated
diseases,
including
autoimmunity,
neurodegeneration,
allergic
conditions,
cancer.
purpose
of
this
review
provide
brief
overview
relationship
between
Siglecs
as
they
relate
human
health
disease,
consider
current
Siglec-based
therapeutics,
discuss
new
therapeutic
approaches
targeting
Siglec-sialic
axis,
with
focus
on
Cancers,
Journal Year:
2022,
Volume and Issue:
14(15), P. 3575 - 3575
Published: July 22, 2022
Immune
checkpoint
inhibitors
(ICIs),
antagonists
used
to
remove
tumor
suppression
of
immune
cells,
have
been
widely
in
clinical
settings.
Their
high
antitumor
effect
makes
them
crucial
for
treating
cancer
after
surgery,
radiotherapy,
chemotherapy,
and
targeted
therapy.
However,
with
the
advent
ICIs
their
use
by
a
large
number
patients,
more
data
gradually
shown
that
some
patients
still
resistance
ICI
treatment,
which
unable
benefit
from
effect.
Therefore,
it
is
vital
understand
drug
mechanisms.
In
this
review,
we
focused
on
action
sites
mechanisms
different
types
ICIs.
We
then
listed
main
possible
based
recent
studies.
Finally,
proposed
current
future
solutions
ICIs,
providing
theoretical
support
improving
Journal of Hematology & Oncology,
Journal Year:
2022,
Volume and Issue:
15(1)
Published: June 7, 2022
Multiple
myeloma
(MM)
is
a
plasma
cell
malignancy
that
affects
an
increasing
number
of
patients
worldwide.
Despite
all
the
efforts
to
understand
its
pathogenesis
and
develop
new
treatment
modalities,
MM
remains
incurable
disease.
Novel
immunotherapies,
such
as
CAR
T
therapy
(CAR)
bispecific
engagers
(BiTE),
are
intensively
targeting
different
surface
antigens,
BMCA,
SLAMF7
(CS1),
GPRC5D,
FCRH5
or
CD38.
However,
stem
transplantation
still
indispensable
in
transplant-eligible
patients.
Studies
suggest
early
use
immunotherapy
may
improve
outcomes
significantly.
In
this
review,
we
summarize
currently
available
clinical
literature
on
BiTE
MM.
Furthermore,
will
compare
these
two
cell-based
immunotherapies
discuss
potential
therapeutic
approaches
promote
development
trials,
using
even
bridging
therapies
transplant.
Cancers,
Journal Year:
2023,
Volume and Issue:
15(4), P. 1189 - 1189
Published: Feb. 13, 2023
Harnessing
the
immune
system
to
fight
cancer
has
become
a
reality
with
clinical
success
of
immune-checkpoint
blockade
(ICB)
antibodies
against
PD(L)-1
and
CTLA-4.
However,
not
all
patients
respond
ICB.
Thus,
there
is
need
modulate
through
alternative
strategies
for
improving
responses
The
CD3-T
cell
receptor
(TCR)
canonical
complex
on
T
cells.
It
provides
"first
signal"
that
initiates
activation
determines
specificity
response.
TCR
confers
binding
whilst
CD3
subunits
facilitate
signal
transduction
necessary
activation.
While
mechanisms
which
antigen
sensing
occur
in
CD3-TCR
are
still
under
debate,
recent
revelations
regarding
intricate
3D
structure
might
open
possibility
modulating
its
activity
by
designing
targeted
drugs
tools,
including
aptamers.
In
this
review,
we
summarize
basis
assembly
survey
preclinical
therapeutic
tools
available
function
potentiating
immunotherapy.