Phenotypic characterization of cells transduced by a lentiviral vector after stimulation with IL-2, IL-7, and IL-15
. | IL-2, % . | . | IL-7, % . | . | IL-15, % . | . | TCR-activated, % . | . | . | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Surface marker . | LNGFr+ . | LNGFr- . | LNGFr+ . | LNGFr- . | LNGFr+ . | LNGFr- . | LNGFr+ . | LNGFr- . | PBMC, % . | ||||
CD3 | >90 | >90 | >90 | >90 | >90 | >90 | >90 | >90 | 87 | ||||
CD4 | 47 | 47 | 48 | 53 | 36 | 44 | 42 | 17 | 53 | ||||
CD8 | 20 | 38 | 26 | 35 | 41 | 35 | 47 | 60 | 32 | ||||
CD56 | 8 | 5 | 4 | 9 | 13 | 18 | 96 | 24 | 12 | ||||
CD62L | 56 | 60 | 54 | 69 | 23 | 45 | 88 | 70 | 33 | ||||
CD95 | 83 | 89 | 90 | 93 | 91 | 91 | 99 | 96 | 40 | ||||
CD25 | 20 | 6 | 23 | 26 | 52 | 43 | 77 | 78 | 1 | ||||
CD16 | 7 | 4 | 5 | 2 | 5 | 7 | 1 | 5 | 5 | ||||
CD14 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | ||||
CD45RA | 50 | 30 | 52 | 40 | 38 | 38 | 11 | 30 | 50 | ||||
CD45RO | 26 | 59 | 28 | 46 | 41 | 46 | 92 | 70 | 49 |
. | IL-2, % . | . | IL-7, % . | . | IL-15, % . | . | TCR-activated, % . | . | . | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Surface marker . | LNGFr+ . | LNGFr- . | LNGFr+ . | LNGFr- . | LNGFr+ . | LNGFr- . | LNGFr+ . | LNGFr- . | PBMC, % . | ||||
CD3 | >90 | >90 | >90 | >90 | >90 | >90 | >90 | >90 | 87 | ||||
CD4 | 47 | 47 | 48 | 53 | 36 | 44 | 42 | 17 | 53 | ||||
CD8 | 20 | 38 | 26 | 35 | 41 | 35 | 47 | 60 | 32 | ||||
CD56 | 8 | 5 | 4 | 9 | 13 | 18 | 96 | 24 | 12 | ||||
CD62L | 56 | 60 | 54 | 69 | 23 | 45 | 88 | 70 | 33 | ||||
CD95 | 83 | 89 | 90 | 93 | 91 | 91 | 99 | 96 | 40 | ||||
CD25 | 20 | 6 | 23 | 26 | 52 | 43 | 77 | 78 | 1 | ||||
CD16 | 7 | 4 | 5 | 2 | 5 | 7 | 1 | 5 | 5 | ||||
CD14 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | ||||
CD45RA | 50 | 30 | 52 | 40 | 38 | 38 | 11 | 30 | 50 | ||||
CD45RO | 26 | 59 | 28 | 46 | 41 | 46 | 92 | 70 | 49 |
Transduced T cells previously stimulated with IL-2, IL-7, and IL-15 or TCR-triggered were characterized for the expression of lineage and activation markers and for transgene expression by flow cytometry. Unmodified PBMCs from the same donors were stained as controls. Transduced and untransduced cells were analyzed and compared by gating on LNGFr+ and LNGFr- cell populations. A representative experiment is shown.