Journal of Clinical & Experimental Immunology,
Journal Year:
2023,
Volume and Issue:
8(3)
Published: July 20, 2023
Not
all
cancer
therapeutic
strategies
known
to
date
are
adequate
for
patients.
Most
of
them
followed
by
a
high
rate
severe
side
effects
and
complications.
L-Tryptophan
metabolism
plays
key
role
in
organism
development,
as
well
the
occurrence
development
tumors.
By
degrading
certain
amino
acids,
tumor
growth
can
be
limited
while
maintaining
body´s
normal
nutritional
requirements.
The
L-tryptophan
depletion
bioreactor
is
described
possible
new
method
therapy.
an
essential
acid
that
has
been
recognized
important
nutrient
its
removal
lead
destruction
cells.
Tumor
cells
or
human
cannot
synthesize
therefore
resistance
unlikely
develop.
also
constituent
different
biomolecules
such
Sero-tonin,
Melatonin,
needed
other
synthesis
processes
cell
growth.
enzymes
with
three
iso-enzymes
called
tryptophan
chain
oxydase
(TSO)
I,
II,
III
have
molecular
weights
effectiveness.
All
TSO
heme
catalyze
essentially
similar
reactions
involving
substrate.
most
effective
type
III.
A
column,
which
contained
TSO,
immobilized
on
silica
beats
bioreactor,
was
integrated
plasmapheresis
unit
tested
it
animals.
In
sheep
rabbits,
plasma
shown
at
95%
100%
rates
respectively
single
pass
through
bioreactor.
20
lines,
there
were
efficacies.
Brest
medulloblastoma
showed
greatest
efficacy
degrading.
gene
technology
production
from
Pseudomonas
associated
formation
endotoxins.
These
endotoxins
must
eliminated.
Bioreactors
developed
treat
diseases
successfully
low
effects.
combination
available
thera-pies
possible.
Nanoscale Advances,
Journal Year:
2024,
Volume and Issue:
6(17), P. 4275 - 4308
Published: Jan. 1, 2024
Chemotherapy
and
surgery
remain
the
primary
treatment
modalities
for
cancers;
however,
these
techniques
have
drawbacks,
such
as
cancer
recurrence
toxic
side
effects,
necessitating
more
efficient
strategies.
Recent
advancements
in
research
medical
technology
provided
novel
insights
expanded
our
understanding
of
development;
consequently,
scholars
investigated
several
delivery
vehicles
therapy
to
improve
efficiency
patient
outcomes.
Herein,
we
summarize
types
smart
therapeutic
carriers
elaborate
on
mechanism
underlying
drug
delivery.
We
reveal
advantages
treatment,
focus
their
effectiveness
immunotherapy,
discuss
application
combination
with
other
emerging
strategies
treatment.
Finally,
bottlenecks
encountered
development
suggest
directions
future
research.
This
review
will
promote
progress
facilitate
related
Medicine,
Journal Year:
2025,
Volume and Issue:
104(10), P. e41548 - e41548
Published: March 7, 2025
AK104
is
a
novel
antibody
targeting
programmed
cell
death
protein
1
(PD-1)/cytotoxic
T-lymphocyte-associated
4.
This
study
aimed
to
evaluate
the
safety,
tolerability,
and
efficacy
of
in
treating
patients
with
advanced
solid
tumors
who
failed
prior
1/programmed
death-ligand
(PD/PD-L1)
therapies.
Clinical
data
from
135
PD/PD-L1
therapies
were
retrospectively
analyzed.
Patients
received
at
dose
6
mg/kg
every
2
weeks.
Baseline
demographic
characteristics,
clinical
outcomes,
adverse
reactions,
overall
survival,
progression-free
quality
life
assessments
Following
treatment,
17.78%
achieved
partial
response,
while
80.74%
experienced
stable
disease,
resulting
disease
control
rate
98.52%.
The
1-
2-year
survival
rates
48.15%
31.11%,
months
year
53.33%
28.15%,
respectively.
Post-treatment,
significant
improvements
quality-of-life
scores,
as
assessed
by
European
Organisation
for
Research
Treatment
Cancer
Quality
Life
Questionnaire-Core
30
EuroQol
5
Dimensions
Visual
Analog
Scale,
observed
post-treatment.
Immune-related
events
common,
affecting
85.19%
patients,
diarrhea,
enteritis,
pneumonia,
thyroid
dysfunction
being
most
frequently
reported.
demonstrated
ability
induce
responses,
extend
enhance
had
previously
PD-1/PD-L1
therapies,
underscoring
its
potential
promising
therapeutic
option.
However,
high
incidence
immune-related
necessitates
vigilant
monitoring
management
maximize
utility.
Further
prospective
studies
are
warranted
validate
these
findings
broader
patient
populations.
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(2), P. 947 - 947
Published: Jan. 12, 2024
Currently,
there
is
a
lack
of
effective
therapies
for
the
majority
glioblastomas
(GBMs),
most
common
and
malignant
primary
brain
tumor.
While
immunotherapies
have
shown
promise
in
treating
various
types
cancers,
they
had
limited
success
improving
overall
survival
GBM
patients.
Therefore,
advancing
treatment
requires
deeper
understanding
molecular
cellular
mechanisms
that
cause
resistance
to
immunotherapy.
Further
insights
into
innate
immune
response
are
crucial
developing
more
potent
treatments
tumors.
Our
review
provides
brief
overview
immunity.
In
addition,
we
provide
discussion
current
aimed
at
boosting
immunity
gliomas.
These
approaches
encompass
strategies
activate
Toll-like
receptors,
induce
stress
responses,
enhance
response,
leverage
interferon
type-I
therapy,
therapeutic
antibodies,
checkpoint
natural
killer
(NK)
cells,
oncolytic
virotherapy,
manipulate
microbiome.
Both
preclinical
clinical
studies
indicate
better
governing
could
immunotherapy
reinforce
effects
chemotherapy
radiotherapy.
Consequently,
comprehensive
against
cancer
should
lead
prognoses
increased
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(11), P. 6266 - 6266
Published: June 6, 2024
Endometriosis
(EMS)
is
an
oestrogen-dependent,
chronic
disease
affecting
women
of
a
reproductive
age.
One
the
important
factors
involved
in
development
this
complex
disorders
associated
with
functioning
immune
system.
Recent
evidence
has
shown
that
EMS
changes
systemic
and
local
immunity,
including
functional
disturbances
effector
antigen-presenting
cells.
reasons
for
imbalance
can
be
improper
expression
checkpoints
(ICPs).
ICPs
their
ligands
are
responsible
maintaining
self-tolerance
modulation
initiation,
duration,
magnitude
response
cells
normal
tissues
to
avoid
tissue
damage.
Considering
nature
co-stimulatory
or
co-inhibitory
signalling
between
APCs,
we
hypothesise
cells'
activity
caused
by
may
lead
serious
system
patients
endometriosis.
Moreover,
both
upregulation
downregulation
implicated
process,
reduced
against
endometrial
implants
process.
In
narrative
review,
discuss,
first
time,
key
findings
from
emerging
literature,
describing
associations
possible
implication
pathogenesis
Biomedicine & Pharmacotherapy,
Journal Year:
2023,
Volume and Issue:
161, P. 114436 - 114436
Published: Feb. 24, 2023
Immunotherapy
has
revolutionized
treatment
of
cancer
during
the
last
decades.
Oncolytic
virotherapy
also
emerged
as
a
strategy
to
fight
against
cells
both
via
lysis
malignant
and
activating
immune
responses.
Accepted
logical
strategy,
combination
monoclonal
antibodies
particularly
programmed
death-1
(PD-1)
death-ligand
1
(PD-L1)
is
introduced
improve
clinical
responses
checkpoint
inhibitors
(ICIs).
Accordingly,
Talimogene
laherparepvec
(T-VEC)
received
approval
for
use,
while
number
oncolytic
Adenoviruses
(Ads)
are
being
investigated
in
trials
malignancies.
Combination
Ads
with
PD-1/PD-L1
have
shown
potentials
promoting
ICIs,
changing
tumor
microenvironment,
inducing
long-term
protection
tumor,
survival
among
mice
models
Regarding
increasing
importance
therapy
cancers,
this
review
we
decide
outline
recent
studies
field.
International Journal of Molecular Sciences,
Journal Year:
2023,
Volume and Issue:
24(15), P. 12056 - 12056
Published: July 27, 2023
DNA
mismatch
repair
deficient
(dMMR)
and
microsatellite
instable
(MSI)
metastatic
colorectal
cancer
(mCRC)
can
be
successfully
treated
with
FDA-
EMA-approved
immune
checkpoint
inhibitors
(ICI)
pembrolizumab
nivolumab
(as
single
agents
targeting
the
anti-programmed
cell
death
protein-1
(PD-1))
or
combinations
of
a
PD-1
inhibitor
ipilimumab,
cytotoxic
T-lymphocyte-associated
protein
4
(CTLA-4)-targeting
antibody.
The
best
treatment
strategy
beyond
progression
on
single-agent
ICI
therapy
remains
unclear.
Here,
we
present
case
63-year-old
male
Lynch-syndrome-associated,
instability-high
(MSI-H)
mCRC
who
achieved
rapid
normalization
his
tumor
markers
complete
metabolic
remission
(CMR),
currently
lasting
for
ten
months,
sequential
combination
ipilimumab
followed
by
maintenance
after
anti-PD-1
therapy.
was
well-tolerated,
no
immune-related
adverse
events
occurred.
To
our
knowledge,
this
is
first
sustained
in
an
MSI-H
patient
initially
progressing
Thus,
dMMR
patients
might
benefit
from
regimens
even
long-term
responses.
However,
further
sophistication
clinical
algorithms
MSI-mCRC
urgently
needed.