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. 2024 Nov 13;32(12):1837–1850. doi: 10.32604/or.2024.056565

Figure A1. Activation of KDA11-01 and KDA11-02 TCR-Transduced Jurkat Cells. Flow cytometry analysis was used to assess the activation of TCR-transduced Jurkat reporter cells in response to specific antigens. (A) shows KDA11-01 TCR-transduced Jurkat reporter cells co-incubated with T2KO-A1101 cells without KD2 peptide loading, serving as a control to establish the gating strategy. (B) demonstrates the activation of KDA11-01 TCR-transduced Jurkat reporter cells following co-incubation with T2KO-A1101 cells loaded with 10−5 M KD2 peptide, indicated by the detection of reporter gene activation through flow cytometry. (C) shows KDA11-02 TCR-transduced Jurkat reporter cells co-incubated with T2KO-A1101 cells without KD2 peptide loading, confirming the gating strategy. (D) illustrates the activation of KDA11-02 TCR-transduced Jurkat reporter cells after co-incubation with T2KO-A1101 cells loaded with 10−5 M KD2 peptide, with reporter gene activation measured by flow cytometry.

Figure A1