Harnessing CD3 diversity to optimize CAR T cells

Abstract: Current US Food and Drug Administration-approved chimeric antigen receptor (CAR) T cells harbor the T cell receptor (TCR)-derived ζ chain as an intracellular activation domain in addition to costimulatory domains. The functionality in a CAR format of the other chains of the TCR complex, namely CD3δ, CD3ε and CD3γ, instead of ζ, remains unknown. In the present study, we have systematically engineered new CD3 CARs, each containing only one of the CD3 intracellular domains. We found that CARs containing CD3δ, CD3ε or CD3γ cytoplasmic tails outperformed the conventional ζ CAR T cells in vivo. Transcriptomic and proteomic analysis revealed differences in activation potential, metabolism and stimulation-induced T cell dysfunctionality that mechanistically explain the enhanced anti-tumor performance. Furthermore, dimerization of the CARs improved their overall functionality. Using these CARs as minimalistic and synthetic surrogate TCRs, we have identified the phosphatase SHP-1 as a new interaction partner of CD3δ that binds the CD3δ–ITAM on phosphorylation of its C-terminal tyrosine. SHP-1 attenuates and restrains activation signals and might thus prevent exhaustion and dysfunction. These new insights into T cell activation could promote the rational redesign of synthetic antigen receptors to improve cancer immunotherapy

Standort
Deutsche Nationalbibliothek Frankfurt am Main
Umfang
Online-Ressource
Sprache
Englisch
Anmerkungen
Nature immunology. - 24, 12 (2023) , 2135-2149, ISSN: 1529-2916

Ereignis
Veröffentlichung
(wo)
Freiburg
(wer)
Universität
(wann)
2023
Urheber
Velasco Cárdenas, Rubí Misol-Há
Brandl, Simon M.
Meléndez Mayorga, Ana Valeria
Schlaak, Alexandra Emilia
Buschky, Annabelle
Peters, Timo
Beier, Fabian
Serrels, Bryan
Taromi, Sanaz
Raute, Katrin
Hauri, Simon
Gstaiger, Matthias
Laßmann, Silke
Huppa, Johannes
Börries, Melanie
Geoffroy, Andrieux
Bengsch, Bertram
Schamel, Wolfgang
Minguet, Susana

DOI
10.1038/s41590-023-01658-z
URN
urn:nbn:de:bsz:25-freidok-2412076
Rechteinformation
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Letzte Aktualisierung
15.08.2025, 07:35 MESZ

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  • 2023

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