Figure 1.
Figure 1. Acute GVHD induced after allogeneic BMT using extensive conditioning in mice with or without PPs. (A) TNFΔ/Δ and TNF-/- mice develop mesenteric LNs and cecal patches (CPs). TNF-/- mice develop PPs, but TNFΔ/Δ mice do not. Not all PPs formed in the TNF-/- mice are visible. Fresh mouse organs, from representative adult naive animals, were photographed using Nikon Coolpix 2500 digital camera set to macro mode. (B) TNFΔ/Δ, TNF-/- mice, or WT mice were used as recipients of allogeneic BM grafts in combination with 3 × 107 spleen cells (SCs) as a source of T cells (n = 9-11 mice/group/experiment). Some groups received BM only to control for non–GVHD-associated changes (n = 3-8 mice/group/experiment). Combined results of 2 independent experiments are shown. No significant differences were observed in mice that received BM and spleen cells. (C) Kinetics of weight loss in one of the 2 independent experiments represented in panel B. (D) TNFΔ/Δ or WT mice were used as recipients of allogeneic BM grafts in combination with 2.5 or 1.25 × 107 spleen cells (SCs) as a source of T cells (n = 5-8 mice/group). Some groups received BM only to control for non–GVHD-associated changes. Representative results of 2 independent experiments are shown for survival kinetics. No significant differences were observed between experimental groups for either dose of spleen cells.

Acute GVHD induced after allogeneic BMT using extensive conditioning in mice with or without PPs. (A) TNFΔ/Δ and TNF-/- mice develop mesenteric LNs and cecal patches (CPs). TNF-/- mice develop PPs, but TNFΔ/Δ mice do not. Not all PPs formed in the TNF-/- mice are visible. Fresh mouse organs, from representative adult naive animals, were photographed using Nikon Coolpix 2500 digital camera set to macro mode. (B) TNFΔ/Δ, TNF-/- mice, or WT mice were used as recipients of allogeneic BM grafts in combination with 3 × 107 spleen cells (SCs) as a source of T cells (n = 9-11 mice/group/experiment). Some groups received BM only to control for non–GVHD-associated changes (n = 3-8 mice/group/experiment). Combined results of 2 independent experiments are shown. No significant differences were observed in mice that received BM and spleen cells. (C) Kinetics of weight loss in one of the 2 independent experiments represented in panel B. (D) TNFΔ/Δ or WT mice were used as recipients of allogeneic BM grafts in combination with 2.5 or 1.25 × 107 spleen cells (SCs) as a source of T cells (n = 5-8 mice/group). Some groups received BM only to control for non–GVHD-associated changes. Representative results of 2 independent experiments are shown for survival kinetics. No significant differences were observed between experimental groups for either dose of spleen cells.

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