Fig. 4.
Fig. 4. Apoptosis rate and cytotoxic activity of B6dom1-specific T cells in B10 versus B10.H7b hosts. / BM cells (107) and spleen cells (5 × 107) from B10.H7b donors preimmunized with B10 splenocytes on day −14 were injected into irradiated (10 Gy) B10 or B10.H7b recipients on day 0. Recipients were injected with 5 × 104 EL4 cells on day +1. (A) Proportion of Annexin V+ cells among tetramer+ and tetramer− CD8 T cells from B10 and B10.H7brecipients. (B) Tetramer staining of CD8 T cells from B10 and B10.H7b mice; numbers indicate the mean fluorescence intensity of tetramer+ cells. (C) Direct cytotoxic activity of CD8 T cells harvested on day 15 after AHCT. Spleen CD8 T cells were enriched by negative depletion of B and CD4 lymphocytes and were cultured for 6 hours at various effector-to-target ratios with [3H]thymidine–labeled EL4 cells (3 mice per group).

Apoptosis rate and cytotoxic activity of B6dom1-specific T cells in B10 versus B10.H7b hosts.

BM cells (107) and spleen cells (5 × 107) from B10.H7b donors preimmunized with B10 splenocytes on day −14 were injected into irradiated (10 Gy) B10 or B10.H7b recipients on day 0. Recipients were injected with 5 × 104 EL4 cells on day +1. (A) Proportion of Annexin V+ cells among tetramer+ and tetramer CD8 T cells from B10 and B10.H7brecipients. (B) Tetramer staining of CD8 T cells from B10 and B10.H7b mice; numbers indicate the mean fluorescence intensity of tetramer+ cells. (C) Direct cytotoxic activity of CD8 T cells harvested on day 15 after AHCT. Spleen CD8 T cells were enriched by negative depletion of B and CD4 lymphocytes and were cultured for 6 hours at various effector-to-target ratios with [3H]thymidine–labeled EL4 cells (3 mice per group).

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