Fig. 4.
Fig. 4. The progeny of GM-CSF and GM-CSF/TNF-α–cultured CD34+/CD86+ cells induce proliferative response of allogeneic CD4+ cells. CD34+/CD86+ and CD34+/CD86− cells were cultured for 9 days in GM-CSF plus SCF, in the absence (B) or presence (C) of TNF-α. Fresh (A) and cultured cells (B and C) were resuspended in 15% PHS. Cells were irradiated at 3,000 cGy, and serial dilutions were cultured with HLA-DR–mismatched CD4+ T cells at 5 × 104 responders/well in U-bottomed plates. Cells were harvested on day 6 after 18 hours of exposure to3H-thymidine.

The progeny of GM-CSF and GM-CSF/TNF-α–cultured CD34+/CD86+ cells induce proliferative response of allogeneic CD4+ cells. CD34+/CD86+ and CD34+/CD86 cells were cultured for 9 days in GM-CSF plus SCF, in the absence (B) or presence (C) of TNF-α. Fresh (A) and cultured cells (B and C) were resuspended in 15% PHS. Cells were irradiated at 3,000 cGy, and serial dilutions were cultured with HLA-DR–mismatched CD4+ T cells at 5 × 104 responders/well in U-bottomed plates. Cells were harvested on day 6 after 18 hours of exposure to3H-thymidine.

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