Figure 3.
Figure 3. Increasing recipient TCR clonotypic variety reduces penetrance and severity of cGVHD. Combined data from 2 experiments. On day 0, recipient mice were lethally irradiated and reconstituted with 8 × 106 BM cells alone (n = 29, all recipient types) or BM plus 107 spleen cells: WT (n = 29), DO11.10 (RAG2+/+) (n = 12), DO11.10 (RAG2-/-) (n = 18), RAG2-/- (n = 16). (A) Incidence of cGVHD. *P < .05 for DO11.10 (RAG2+/+) versus WT and versus RAG2-/-; P = .094 for DO11.10 (RAG2+/+) versus DO11.10 (RAG2-/-). (B) Pathology score for representative mice. Mean score is indicated by a horizontal bar. *P < .05 for DO11.10 (RAG2+/+) versus DO11.10 (RAG2-/-) and versus RAG2-/-. Pathology samples were taken on day 24, 28, or 50.

Increasing recipient TCR clonotypic variety reduces penetrance and severity of cGVHD. Combined data from 2 experiments. On day 0, recipient mice were lethally irradiated and reconstituted with 8 × 106 BM cells alone (n = 29, all recipient types) or BM plus 107 spleen cells: WT (n = 29), DO11.10 (RAG2+/+) (n = 12), DO11.10 (RAG2-/-) (n = 18), RAG2-/- (n = 16). (A) Incidence of cGVHD. *P < .05 for DO11.10 (RAG2+/+) versus WT and versus RAG2-/-; P = .094 for DO11.10 (RAG2+/+) versus DO11.10 (RAG2-/-). (B) Pathology score for representative mice. Mean score is indicated by a horizontal bar. *P < .05 for DO11.10 (RAG2+/+) versus DO11.10 (RAG2-/-) and versus RAG2-/-. Pathology samples were taken on day 24, 28, or 50.

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