Figure 3
IL-15-dependent engraftment of CMV-specific TCM/E cells in NOG mice is greater than that of TEM/E. (A) Schematic of the experiment. (B) Mean percentage (± SE) of human T cells (CD45+ CD8+) in peripheral blood lymphocytes (PBLs) of mice engrafted with TCM/E (squares) or TEM/E (circles) was determined by flow cytometry (n = 5). *P < .05, TCM/E versus TEM/E cell engraftment in the presence of NS0-IL-15 cells (unpaired Student t test). (Inset) Mean levels of human IL-15 (± SE) in day 7 serum of NOG mice that had received 3 intraperitoneal injections of 1.5 × 107 irradiated NS0-IL-15 cells (n = 6) or in control mice (n = 10). (C) Mean percentage of human T cells (CD45+ CD8+) plus or minus SE in mouse PBL, bone marrow, and spleen at day 21. *P < .05, TCM/E cell engraftment in each organ versus that of TEM/E in the presence of NS0-IL-15 cells. (D) TCR Vβ repertoire of the CMV-specific TCM/E and TEM/E before (Input) and after (d21) engraftment. Percentage of CD3+ cells (Input) or CD45+ CD3+ cells (d21) that were positive for the indicated TCR Vβ genes was determined by flow cytometry.

IL-15-dependent engraftment of CMV-specific TCM/E cells in NOG mice is greater than that of TEM/E. (A) Schematic of the experiment. (B) Mean percentage (± SE) of human T cells (CD45+ CD8+) in peripheral blood lymphocytes (PBLs) of mice engrafted with TCM/E (squares) or TEM/E (circles) was determined by flow cytometry (n = 5). *P < .05, TCM/E versus TEM/E cell engraftment in the presence of NS0-IL-15 cells (unpaired Student t test). (Inset) Mean levels of human IL-15 (± SE) in day 7 serum of NOG mice that had received 3 intraperitoneal injections of 1.5 × 107 irradiated NS0-IL-15 cells (n = 6) or in control mice (n = 10). (C) Mean percentage of human T cells (CD45+ CD8+) plus or minus SE in mouse PBL, bone marrow, and spleen at day 21. *P < .05, TCM/E cell engraftment in each organ versus that of TEM/E in the presence of NS0-IL-15 cells. (D) TCR Vβ repertoire of the CMV-specific TCM/E and TEM/E before (Input) and after (d21) engraftment. Percentage of CD3+ cells (Input) or CD45+ CD3+ cells (d21) that were positive for the indicated TCR Vβ genes was determined by flow cytometry.

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