High-affinity T cell receptors for adoptive cell transfer.


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:
02 01 2019
Historique:
pubmed: 12 12 2018
medline: 31 10 2019
entrez: 12 12 2018
Statut: ppublish

Résumé

Adoptive cell transfer (ACT) of engineered T cell receptors (TCRs) for cancer immunotherapy has evolved from simple gene transfer of isolated TCRs to various affinity enhancement techniques that overcome limitations imposed by central and peripheral tolerance on TCR affinity. In the current issue of the JCI, Poncette et al. used mice with human TCRαβ and HLA gene loci to discover CD4+ TCRs of optimal affinity for cancer testis antigen (CTA) NY-ESO-1. They combined this TCR with a previously discovered NY-ESO-1-specific CD8+ TCR in an ACT fibrosarcoma tumor model to demonstrate the importance of T cell help in mediating antitumor responses.

Identifiants

pubmed: 30530992
pii: 125471
doi: 10.1172/JCI125471
pmc: PMC6307956
doi:
pii:

Substances chimiques

Antigens, Neoplasm 0
Receptors, Antigen, T-Cell 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Comment

Langues

eng

Sous-ensembles de citation

IM

Pagination

69-71

Subventions

Organisme : NIAID NIH HHS
ID : P01 AI072677
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA108835
Pays : United States
Organisme : NCI NIH HHS
ID : R21 CA185819
Pays : United States
Organisme : NIBIB NIH HHS
ID : R21 EB023411
Pays : United States

Commentaires et corrections

Type : CommentOn

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Auteurs

Ariel Isser (A)

Department of Biomedical Engineering.

Jonathan P Schneck (JP)

Department of Pathology, Medicine and Oncology, and.
Immunology Program, Institute of Cellular Engineering, Johns Hopkins University, School of Medicine, Baltimore, Maryland, USA.

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Classifications MeSH