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. Author manuscript; available in PMC: 2009 Jan 22.
Published in final edited form as: J Immunol. 2007 Nov 1;179(9):5936–5946. doi: 10.4049/jimmunol.179.9.5936

FIGURE 2.

FIGURE 2

Diabetes recurred more slowly in diabetic NOD-RIP-CD80 mice. A, Transplant survival was monitored in diabetic NOD, NOD-RIP-CD80, and NOD-RIP-CD86 mice in which islets from 6-wk-old NOD mice were transplanted under the kidney capsule and rendered euglycemic after 48 h. The difference in time of development of recurrent diabetes was statistically significant (p < 0.05). B, Cellular phenotypes infiltrating transplanted islets in diabetic NOD (Tg negative (−ve)), NOD-RIP-CD80, and NOD-RIP-CD86 were examined by immunohistochemistry on frozen sections.