Figure 5.
Figure 5. Donor T cell-derived TNF-α critically contributes to the development of IPS. Lethally irradiated B6D2F1 mice underwent transplantation as described in Figure 2 (syngeneic, ▥; allogeneic wild-type, ▪; allogeneic TNF-α-/-, ▦). A third allogeneic group received allogeneic TNF-α+/+ bone marrow cells mixed with allogeneic TNF-α-/- T cells (▥). Lung injury was assessed 35 days after transplantation by lung histopathology (A), BAL cellularity (B), and BAL fluid TNF-α levels (C). Data are presented as mean ± SEM and are from 1 of 2 comparable experiments; n = 4 to 8 per group; *P < .05, ▦ and ▥ versus ▪.

Donor T cell-derived TNF-α critically contributes to the development of IPS. Lethally irradiated B6D2F1 mice underwent transplantation as described in Figure 2 (syngeneic, ▥; allogeneic wild-type, ▪; allogeneic TNF-α-/-, ▦). A third allogeneic group received allogeneic TNF-α+/+ bone marrow cells mixed with allogeneic TNF-α-/- T cells (▥). Lung injury was assessed 35 days after transplantation by lung histopathology (A), BAL cellularity (B), and BAL fluid TNF-α levels (C). Data are presented as mean ± SEM and are from 1 of 2 comparable experiments; n = 4 to 8 per group; *P < .05, ▦ and ▥ versus ▪.

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