How personalized cancer vaccines could keep tumours from coming back
Elie Dolgin
No information about this author
Nature,
Journal Year:
2024,
Volume and Issue:
630(8016), P. 290 - 292
Published: June 11, 2024
The
same
mRNA
technology
that
quickly
brought
the
world
a
vaccine
for
COVID-19
is
now
showing
promise
as
bespoke
therapy
cancer.
Language: Английский
Comparative performance analysis of neoepitope prediction algorithms in head and neck cancer
Leila Y. Chihab,
No information about this author
Julie G. Burel,
No information about this author
Aaron M. Miller
No information about this author
et al.
Frontiers in Immunology,
Journal Year:
2025,
Volume and Issue:
16
Published: March 4, 2025
Background
Mutations
in
cancer
cells
can
result
the
production
of
neoepitopes
that
be
recognized
by
T
and
trigger
an
immune
response.
A
reliable
pipeline
to
identify
such
immunogenic
for
a
given
tumor
would
beneficial
design
immunotherapies.
Current
methods,
as
proposed
Tumor
Neoantigen
Selection
Alliance
(TESLA),
aim
select
short
peptides
with
highest
likelihood
MHC-I
restricted
minimal
epitopes.
Typically,
only
small
percentage
these
predicted
epitopes
are
when
tested
experimentally.
This
is
particularly
problematic
limited
amount
sample
available
from
patients
acutely
sick
restricts
number
practice.
led
our
group
develop
in-house
termed
Identify-Prioritize-Validate
(IPV)
identifies
long
cover
both
CD4
CD8
Methods
Here,
we
systematically
compared
how
IPV
performs
TESLA
pipeline.
Patient
peripheral
blood
mononuclear
were
cultured
vitro
their
corresponding
candidate
peptides,
recognition
was
measured
using
cytokine-secretion
assays.
Results
The
consistently
outperformed
predicting
elicited
response
assay.
primarily
due
inclusion
longer
TESLA.
Conclusions
Our
work
underscores
improved
predictive
ability
comparison
this
assay
system
highlights
need
clearly
define
which
experimental
metrics
used
evaluate
bioinformatic
epitope
predictions.
Language: Английский
MHC class II-mediated spontaneous rejection of breast carcinomas expressing model neoantigens
James W. Jenkins,
No information about this author
Alvaro Peña,
No information about this author
Sarah A Castro
No information about this author
et al.
Journal for ImmunoTherapy of Cancer,
Journal Year:
2025,
Volume and Issue:
13(4), P. e010434 - e010434
Published: April 1, 2025
Background
Cancers
persist
despite
expression
of
immunogenic
neoantigens
and
ongoing
antitumor
immune
responses.
While
some
occult
tumors
likely
are
cleared
by
effective
responses,
the
targeted
antigens
not
easily
identifiable
as
those
spontaneously
disappear.
Methods
We
used
mouse
models
with
a
defined
antigenic
protein
mimicking
tumor-specific
to
address
nature
these
spontaneous
anti-tumor
Results
BALB/c
(
H-2
d
)
mice
challenged
breast
expressing
rat-erbB2
oncoprotein
succumb
their
responses
targeting
model
antigens.
Meanwhile,
congenic
BALB.B
b
/H-2
F1
hybrid
eliminate
genetically
matched
in
major
histocompatibility
complex
(MHC)-II
dependent
manner.
Adoptive
transfer
cell
depletion
strategies
revealed
CD4+
T
cells
CD20+
B
crucial
mediators
protective
response
mice.
Furthermore,
passive
serum
from
rejecting
confers
resistance
tumor
antigen-tolerant
animals
an
inversely
proportional
relationship
between
outgrowth
amount
specific
antibody
present
tumor-bearing
Introduction
rat-erb2
ectodomain
into
other
also
promotes
rejection.
Notably,
microenvironments
differ
rat-erbB2+
at
time
fate
decision
reflecting
differences
ineffective
Conclusions
find
that
immunity
cancer
is
determined
MHC-II-restricted
presentation
optimal
cancer-associated
These
on
cells,
antigen-specific
antibodies.
Language: Английский
mRNA cancer vaccines: features of problems and collisions
Molecular Genetics Microbiology and Virology (Russian),
Journal Year:
2025,
Volume and Issue:
43(1), P. 3 - 3
Published: April 10, 2025
The
article
examines
the
structural
organization
of
vaccine
mRNA,
classification
tumor
antigens,
lessons
from
use
mRNA
in
Covid19
pandemic,
possibility
including
genome
vaccinated,
limitations
immune
system
terms
existence
a
continuum
protein
affinity
evolutionary
hierarchy
organisms,
causes
weak
immunogenicity
neoantigens.
restrictions
on
tripeptides
primary
structure
human
proteins
and
viruses
pathogenic
to
it
is
shown.
results
analysis
homology
between
several
canonical
non-canonical
neoantigens
various
are
presented.
Collisions
with
considered
aspect
an
immunoepitope
affinity,
which
emergence
auto-tolerance
Undetected
or
rarely
occurring
viral
can
be
used
as
potential
biomarkers
predict
similarity
epitopes
proteins,
infection
induces
lifelong
immunity,
discussed
possible
biomarker
immunodominance
induce
long-term
memory.
Language: Английский
Vaccines as Prophylactics and Therapeutics
Published: Jan. 1, 2025
Language: Английский
CIMT 2024: Report on the 21st Annual Meeting of the Association for Cancer Immunotherapy
Yasemin Ahrberg,
No information about this author
Julia Dallmann,
No information about this author
Janina Freitag
No information about this author
et al.
Human Vaccines & Immunotherapeutics,
Journal Year:
2024,
Volume and Issue:
20(1)
Published: July 23, 2024
The
21st
Association
for
Cancer
Immunotherapy
(CIMT)
Annual
Meeting
took
place
from
May
15th
to
17th
in
Mainz,
Germany,
and
was
attended
by
a
total
of
855
academic
clinical
professionals
hailing
33
different
countries.
conference
served
as
platform
these
experts
convene
discuss
the
latest
breakthroughs
cancer
immunology
immunotherapy
research.
Dedicated
sessions
covering
advancements
artificial
intelligence
tools
research,
well
landscape
care
trials
on
African
continent,
prompted
lively
informative
discussions
among
attendees.
This
report
aims
provide
an
overview
most
noteworthy
highlights
key
takeaways
CIMT2024.
Language: Английский