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. Author manuscript; available in PMC: 2015 May 11.
Published in final edited form as: J Immunol. 2004 Jun 15;172(12):7451–7458. doi: 10.4049/jimmunol.172.12.7451

FIGURE 5.

FIGURE 5

Histological assessment of cardiac allografts. a, C57BL/6 donor allograft harvested from a BALB/c rag−/− recipient left unreconstituted at >60 days demonstrating normal cardiomyocytes and vasculature without evidence of rejection. b, C57BL/6 control donor allograft rejected in BALB/c rag−/− recipient reconstituted with enriched CD4+ T cells demonstrating a moderate to severe lymphocytic infiltration and cardiomyocyte necrosis. c, B6 → C2D chimeric donor allograft (MHC class II expression isolated to the bone marrow-derived compartment) harvested 60 days after CD4+ T cell transfer demonstrating mild lymphocytic infiltration, relatively intact cardiomyocytes, and no obvious evidence of necrosis. d, B6 → B6 control chimeric donor allograft demonstrating moderate to severe lymphocytic infiltration and cardiomyocyte necrosis similar to that of C57BL/6 control allografts. e, C2D → B6 (MHC class II expression isolated to the somatic compartment) harvested 60 days after CD4+ T cell transfer demonstrating mild lymphocytic infiltration and mild cardiomyocyte damage (some minimal early necrosis). f, C2D → B6 donor allograft rejected 18 days after CD4+ T cell transfer and 16 days after transfer of C57BL/6 rag−/− splenocytes (source of MHC class II+ APCs) demonstrating moderate to severe lymphocytic infiltration and cardiomyocyte necrosis. Immunoperoxidase staining for CD4 and CD8 demonstrated CD4+ staining and a lack of CD8+ staining in all allografts (data not shown).