Cancer neoantigens targeted by adoptive T cell transfer: private no more.


Journal

The Journal of clinical investigation
ISSN: 1558-8238
Titre abrégé: J Clin Invest
Pays: United States
ID NLM: 7802877

Informations de publication

Date de publication:
01 03 2019
Historique:
pubmed: 5 2 2019
medline: 18 2 2020
entrez: 5 2 2019
Statut: ppublish

Résumé

Effector T cell responses directed toward cancer neoantigens mediate tumor regression following checkpoint blockade or adoptive T cell immunotherapy, but are generally "private", thus requiring considerable effort for their identification. In this issue of the JCI, Malekzadeh et al. show that a fraction of patients with epithelial cancers mount antigen-specific T cell responses to "hot spot" p53 mutations that in some cases are shared among patients. This work suggests that other genes frequently mutated in human cancer can be immunogenic, thus offering a rapid way to screen for cancer neoantigens that can be targeted by subsequent T cell-based therapies.

Identifiants

pubmed: 30714989
pii: 126295
doi: 10.1172/JCI126295
pmc: PMC6391111
doi:
pii:

Substances chimiques

Antigens, Neoplasm 0
TP53 protein, human 0
Tumor Suppressor Protein p53 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Comment

Langues

eng

Sous-ensembles de citation

IM

Pagination

949-951

Commentaires et corrections

Type : CommentOn

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Auteurs

Enrico Lugli (E)

Laboratory of Translational Immunology and.
Flow Cytometry Core, Humanitas Clinical and Research Center, Rozzano, Milan, Italy.

Pia Kvistborg (P)

Division of Molecular Oncology and Immunology, The Netherlands Cancer Institute, Amsterdam, Netherlands.

Giovanni Galletti (G)

Laboratory of Translational Immunology and.

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Classifications MeSH