Figure 4
Figure 4. Cilengitide administration allows for CD8-mediated cytotoxicity. Allo-HCT was performed as described. (A) CD4+/CD8+ Tc’s were isolated from BALB/c recipients on day 14 after allo-HCT and cilengitide or PBS treatment and used as effector cells against L1210 cells in the indicated ratios of target:effector. Values are the percentage of annexin V+/PI+ cells ± SD from 1 representative experiment. Experiments were repeated 3 times in triplicates with similar results. (B-C) Splenocytes were isolated on day 14 after allo-HCT from BALB/c recipients and stained for CD8 and CD107a. (B) Quantification of CD107a+ population as percentage ± SD of all CD8+ Tc’s. One representative of 2 independent experiments is shown, each performed with at least 4 animals per group. (C) Representative flow cytometry data for the indicated groups described in (B) are shown. (D) Expansion and rejection of A20luc cells in BALB/c recipients receiving BM alone, with Tc’s and PBS or cilengitide. Days 0, 6, and 13 as representative time points are shown (left panel). Photons emitted from the A20luc cells in vivo are shown over time for the indicated groups (n = 3 per group). The experiment was performed 3 times with at least 3 animals per group and showed similar results (right panel). (E) Mice from the indicated groups were euthanized on day 13 after allo-HCT. LN (axillary, mesenteric, inguinal) and BM from the femur was isolated and analyzed for the presence of B220high A20luc cells by flow cytometry. The percentage (mean ± SD) of B220high A20luc cells in the BM (left) and LN (right panel) is shown. The experiment was performed once with at least 3 mice in each group. (F) Survival of BALB/c recipients after allo-HCT receiving additional A20luc and PBS or cilengitide. Survival is improved in the BM/A20luc+Tc+cilengitide-treated group () as compared with BM/A20luc+Tc+PBS (; P = .005), BM/A20luc+cilengitide (; P = .025), and BM/A20luc alone (; P = .003). The experiment was performed twice, and the number of mice per group is indicated in the survival graph.

Cilengitide administration allows for CD8-mediated cytotoxicity. Allo-HCT was performed as described. (A) CD4+/CD8+ Tc’s were isolated from BALB/c recipients on day 14 after allo-HCT and cilengitide or PBS treatment and used as effector cells against L1210 cells in the indicated ratios of target:effector. Values are the percentage of annexin V+/PI+ cells ± SD from 1 representative experiment. Experiments were repeated 3 times in triplicates with similar results. (B-C) Splenocytes were isolated on day 14 after allo-HCT from BALB/c recipients and stained for CD8 and CD107a. (B) Quantification of CD107a+ population as percentage ± SD of all CD8+ Tc’s. One representative of 2 independent experiments is shown, each performed with at least 4 animals per group. (C) Representative flow cytometry data for the indicated groups described in (B) are shown. (D) Expansion and rejection of A20luc cells in BALB/c recipients receiving BM alone, with Tc’s and PBS or cilengitide. Days 0, 6, and 13 as representative time points are shown (left panel). Photons emitted from the A20luc cells in vivo are shown over time for the indicated groups (n = 3 per group). The experiment was performed 3 times with at least 3 animals per group and showed similar results (right panel). (E) Mice from the indicated groups were euthanized on day 13 after allo-HCT. LN (axillary, mesenteric, inguinal) and BM from the femur was isolated and analyzed for the presence of B220high A20luc cells by flow cytometry. The percentage (mean ± SD) of B220high A20luc cells in the BM (left) and LN (right panel) is shown. The experiment was performed once with at least 3 mice in each group. (F) Survival of BALB/c recipients after allo-HCT receiving additional A20luc and PBS or cilengitide. Survival is improved in the BM/A20luc+Tc+cilengitide-treated group () as compared with BM/A20luc+Tc+PBS (; P = .005), BM/A20luc+cilengitide (; P = .025), and BM/A20luc alone (; P = .003). The experiment was performed twice, and the number of mice per group is indicated in the survival graph.

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