Figure 5.
Figure 5. Treatment with DCVIPs does not abrogate cytotoxicity of transplanted T cells against leukemic cells. GVHD was induced in recipient Balb/c (H-2d) mice by allogeneic transplantation of BMS from B6 (H-2b) mice. Two days after transplantation, recipients were given injections of medium (none) or with BM-DCs from Balb/c (H-2d) generated in the absence (DCcontrols) or presence (DCVIPs) of VIP. (A) Donor I-KbCD8+ cells isolated from recipient spleens (untreated, •; DCcontrols-treated, ○; DCVIPs-treated, ▾) were subjected to cytotoxicity assays against leukemia A20 (H-2d) and mastocytoma P815 (H-2d) cells (n = 8). (B) Donor I-KbCD8+ cells isolated from recipient spleens were analyzed for CD44 and CD62L expression by flow cytometry. Numbers represent the percentage of cells in each quadrant. Result is representative of 8 identical experiments.

Treatment with DCVIPs does not abrogate cytotoxicity of transplanted T cells against leukemic cells. GVHD was induced in recipient Balb/c (H-2d) mice by allogeneic transplantation of BMS from B6 (H-2b) mice. Two days after transplantation, recipients were given injections of medium (none) or with BM-DCs from Balb/c (H-2d) generated in the absence (DCcontrols) or presence (DCVIPs) of VIP. (A) Donor I-KbCD8+ cells isolated from recipient spleens (untreated, •; DCcontrols-treated, ○; DCVIPs-treated, ▾) were subjected to cytotoxicity assays against leukemia A20 (H-2d) and mastocytoma P815 (H-2d) cells (n = 8). (B) Donor I-KbCD8+ cells isolated from recipient spleens were analyzed for CD44 and CD62L expression by flow cytometry. Numbers represent the percentage of cells in each quadrant. Result is representative of 8 identical experiments.

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