WO2023111322 - GLYCO-ENGINEERED CAR-T CELLS

National phase entry:
Publication Number WO/2023/111322
Publication Date 22.06.2023
International Application No. PCT/EP2022/086474
International Filing Date 16.12.2022
Title **
[English] GLYCO-ENGINEERED CAR-T CELLS
[French] CELLULES CAR-T GLYCO-MODIFIÉES
Applicants **
VIB VZW Suzanne Tassierstraat 1 9052 Gent, BE
UNIVERSITEIT GENT Sint-Pietersnieuwstraat 25 9000 Gent, BE
Inventors
CALLEWAERT, Nico Begijnhoflaan 15 9850 Nevele, BE
FESTJENS, Nele Bruggestraat 35 9690 Kluisbergen, BE
DE BOUSSER, Elien Guldenmeers 13 9050 Gent, BE
Priority Data
21215482.7   17.12.2021   EP
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Quotation for National Phase entry

Country StagesTotal
China Filing1519
EPO Filing, Examination5896
Japan Filing529
South Korea Filing575
USA Filing, Examination5635
MasterCard Visa

Total: 14154

The term for entry into the National Phase has expired. This quotation is for informational purposes only

Abstract[English] gene, as to provide for surface glycan structures devoid of tetra-antennary N-glycans, which results in a sustained memory when applied in immunotherapy, to cure cancer, reduce (recurrent) tumor growth and tumor burden, as well as to prevent relapse. The invention further relates to methods for manufacturing of those CAR-T cells, wherein addition of low amounts of DMSO during activation and expansion ex vivo skews T cell populations to a more predominant memory phenotype, thereby providing for improved glycol- engineered CAR-T cell compositions for adoptive T cell transfer.[French] muté, de manière à fournir des structures de glycane de surface dépourvues de N-glycanes tétra-antennaires, ce qui permet d'obtenir une mémoire soutenue lors d'une application en immunothérapie, de guérir le cancer, de réduire la croissance tumorale (récurrente) et la charge tumorale, ainsi que d'empêcher une rechute. L'invention concerne en outre des procédés de fabrication de ces cellules CAR-T, l'ajout de faibles quantités de DMSO pendant l'activation et l'expansion ex vivo orientant les populations de lymphocytes T vers un phénotype de mémoire plus prédominant, ce qui permet d'obtenir des compositions de cellules CAR-T modifiées par glycol améliorées pour un transfert adoptif de lymphocytes T.
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