Homeostatic proliferation of Des-TCR CD8 T cells does not break tolerance
Donor mouse . | Incidence of tumor growth (P815.Kb.B7) . | |
---|---|---|
1 | No cell transfer | 14 of 14 |
2 | Des-TCR.RAG2−/− | 0 of 7 |
3 | Des-TCR.RAG2−/− (Tx) | 2 of 7 |
4 | Des-TCR × 2.4KerIV-Kb.RAG2−/− (Tx) | 14 of 15 |
Donor mouse . | Incidence of tumor growth (P815.Kb.B7) . | |
---|---|---|
1 | No cell transfer | 14 of 14 |
2 | Des-TCR.RAG2−/− | 0 of 7 |
3 | Des-TCR.RAG2−/− (Tx) | 2 of 7 |
4 | 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.