An Empirical Antigen Selection Method Identifies Neoantigens That Either Elicit Broad Antitumor T-cell Responses or Drive Tumor Growth.
Animals
Antigens, Neoplasm
/ genetics
Biomarkers, Tumor
/ genetics
Cancer Vaccines
/ administration & dosage
Cell Line, Tumor
Clinical Trials as Topic
DNA Mutational Analysis
Disease Models, Animal
Disease Progression
Genomics
/ methods
Humans
Immunity, Cellular
Immunogenicity, Vaccine
Melanoma, Experimental
Mice
Mutation
Neoplasms
/ genetics
T-Lymphocytes
/ immunology
Treatment Outcome
Vaccination
Journal
Cancer discovery
ISSN: 2159-8290
Titre abrégé: Cancer Discov
Pays: United States
ID NLM: 101561693
Informations de publication
Date de publication:
03 2021
03 2021
Historique:
received:
15
04
2020
revised:
15
09
2020
accepted:
13
11
2020
pubmed:
29
1
2021
medline:
20
1
2022
entrez:
28
1
2021
Statut:
ppublish
Résumé
Neoantigens are critical targets of antitumor T-cell responses. The ATLAS bioassay was developed to identify neoantigens empirically by expressing each unique patient-specific tumor mutation individually in
Identifiants
pubmed: 33504579
pii: 2159-8290.CD-20-0377
doi: 10.1158/2159-8290.CD-20-0377
doi:
Substances chimiques
Antigens, Neoplasm
0
Biomarkers, Tumor
0
Cancer Vaccines
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
696-713Informations de copyright
©2021 American Association for Cancer Research.
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