Figure 6
Figure 6. Effect of H60 vaccination on TM recipients. B6.H60 → actH60 mice were irradiated and reconstituted with T cell–depleted C3H.SW BM with no T cells or 5 × 105 CD8+ TM from DEC-H60–vaccinated or unmanipulated C3H.SW donors. Additional positive GVHD control groups received 5 × 105 or 106 TN from unmanipulated C3H.SW donors. As measured by weight change (A) and survival (B), neither CD8+ TM from DEC-H60–vaccinated nor those from unmanipulated C3H.SW mice induced clinical GVHD. P > .07 comparing percent weight change of TMH60 and BM controls at all days except days +3 and +24. P ≥ .29 comparing weight change in TMH60 and TM recipients at all days except day +3. P ≥ .4561 comparing survival in BM alone with the TMH60 or TM group; P ≤ .0109 comparing BM alone recipients with either TN group. Neither TM nor TMH60 cells induced histopathologic skin, ear, or colon GVHD (P > .12 compared with BM alone controls). However, TMH60 induced GVHD in the liver compared with TM or BM alone groups (P = .0015). TM and TMH60 recipients had similar scores in all other tissues (P ≥ .2). In contrast, both TN doses induced significant ear GVHD and 106 TN induced skin, colon, and liver pathology (P ≤ .04 compared with BM alone controls). TetH60+ cells expanded in TMH60 recipients. (D) Representative flow cytometry at day +14. Data are combined from 2 experiments with similar results.

Effect of H60 vaccination on TM recipients. B6.H60 → actH60 mice were irradiated and reconstituted with T cell–depleted C3H.SW BM with no T cells or 5 × 105 CD8+ TM from DEC-H60–vaccinated or unmanipulated C3H.SW donors. Additional positive GVHD control groups received 5 × 105 or 106 TN from unmanipulated C3H.SW donors. As measured by weight change (A) and survival (B), neither CD8+ TM from DEC-H60–vaccinated nor those from unmanipulated C3H.SW mice induced clinical GVHD. P > .07 comparing percent weight change of TMH60 and BM controls at all days except days +3 and +24. P ≥ .29 comparing weight change in TMH60 and TM recipients at all days except day +3. P ≥ .4561 comparing survival in BM alone with the TMH60 or TM group; P ≤ .0109 comparing BM alone recipients with either TN group. Neither TM nor TMH60 cells induced histopathologic skin, ear, or colon GVHD (P > .12 compared with BM alone controls). However, TMH60 induced GVHD in the liver compared with TM or BM alone groups (P = .0015). TM and TMH60 recipients had similar scores in all other tissues (P ≥ .2). In contrast, both TN doses induced significant ear GVHD and 106 TN induced skin, colon, and liver pathology (P ≤ .04 compared with BM alone controls). TetH60+ cells expanded in TMH60 recipients. (D) Representative flow cytometry at day +14. Data are combined from 2 experiments with similar results.

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