Figure S4 from Targeting SALL4 with an HLA Class I–Restricted TCR for Cancer Immunotherapy

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Authors: Myriam Ben Khelil, Maxime Fredon, Nawfel Adib, Adeline Bouard, Marie Perchaud, Syrine Abdeljaoued, Charles-Frédéric Mantion, Kamal Asgarov, Philippe Guillaume, Laurie Spehner, Evan Seffar, Marjorie Labesse
+13 more Angélique Vienot, Virginie Mougey, Mathieu Gonçalves-Venturelli, Sara Bobisse, Alexandre Harari, Camilla Jandus, Francine Garnache‐Ottou, Delphine Binda, Olivier Adotévi, Yann Godet, Marie Kroemer, Christophe Borg, Romain Loyon
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Abstract

SALL4-derived S9V specific CD8+ T clone recognize and kill MDA-MB231-SALL4 cell line in vitro. Mean number of IFN-γ (left) and GZMB (right) spots counted on ELISpot upon 24h coculture of SALL4 specific CD8+ T clone with MDA-MB231-SALL4 with different E:T ratio 10:1, 5:1, 1:1, 1:5 and 1:10. Data represent mean ± SD of duplicates. Responses were considered positive if the number of SFC was > 10 spots/104 T clone and 2 times the background value. MDA-MB231-CTRL cell line transduced with empty lentiviral vector was used as negative control. Anti MHC-I antibody was used for specific T cell restriction reactivation validation.

Fields of Study & Subjects

Renal and related cancers CAR-T cell therapy research Pluripotent Stem Cells Research

Publication details

Publication date
8 January 2026