Journal article
The chimeric TAC receptor co-opts the T cell receptor yielding robust anti-tumor activity without toxicity
Abstract
Engineering T cells with chimeric antigen receptors (CARs) is an effective method for directing T cells to attack tumors, but may cause adverse side effects such as the potentially lethal cytokine release syndrome. Here the authors show that the T cell antigen coupler (TAC), a chimeric receptor that co-opts the endogenous TCR, induces more efficient anti-tumor responses and reduced toxicity when compared with past-generation CARs. …
Authors
Helsen CW; Hammill JA; Lau VWC; Mwawasi KA; Afsahi A; Bezverbnaya K; Newhook L; Hayes DL; Aarts C; Bojovic B
Journal
Nature Communications, Vol. 9, No. 1,
Publisher
Springer Nature
DOI
10.1038/s41467-018-05395-y
ISSN
2041-1723
Associated Experts
Fields of Research (FoR)
Medical Subject Headings (MeSH)
Adoptive TransferAnimalsCD28 AntigensCell Line, TumorCytokinesCytotoxicity, ImmunologicFemaleGenetic EngineeringHEK293 CellsHumansImmunotherapy, AdoptiveLentivirusLymphocyte ActivationMaleMiceMice, Inbred NODProtein EngineeringReceptor, ErbB-2Receptors, AntigenReceptors, Chimeric AntigenRecombinant ProteinsSingle-Domain AntibodiesT-Cell Antigen Receptor SpecificityT-LymphocytesT-Lymphocytes, CytotoxicVision, OcularXenograft Model Antitumor Assays