Table 1

Homeostatic proliferation of Des-TCR CD8 T cells does not break tolerance

Donor mouseIncidence of tumor growth (P815.Kb.B7)
No cell transfer 14 of 14 
Des-TCR.RAG2−/− 0 of 7 
Des-TCR.RAG2−/− (Tx) 2 of 7 
Des-TCR × 2.4KerIV-Kb.RAG2−/− (Tx) 14 of 15 
Donor mouseIncidence of tumor growth (P815.Kb.B7)
No cell transfer 14 of 14 
Des-TCR.RAG2−/− 0 of 7 
Des-TCR.RAG2−/− (Tx) 2 of 7 
Des-TCR × 2.4KerIV-Kb.RAG2−/− (Tx) 14 of 15 

Thirty thousand MACS-purified Des-TCR CD8 T cells from reactive Des-TCR.RAG2−/−, thymectomized reactive Des-TCR.RAG2−/−, and thymectomized tolerant Des-TCR × 2.4KerIV-Kb.RAG2−/− donor mice were transferred intravenously into RAG2−/− mice. After 3 days the mice were challenged subcutaneously with 2 × 105 P815.Kb.B7 tumor cells and the mice were then analyzed for tumor growth. After 14 to 18 days, most tumor-bearing mice had to be sacrificed due to the size of the tumors. Tumor-free mice were continued to be observed. The summarized data are from 3 independent experiments.

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