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. 2004 Mar 2;101(11):3892–3897. doi: 10.1073/pnas.0400138101

Fig. 1.

Fig. 1.

(A) The process of spontaneous transgenesis and immunization with transgenic lymphocytes. Details of the two procedures are described in Materials and Methods. (B) The characteristics of the primary CD4 T cell response: kinetics and specificity. C57BL/6 mice were injected with 5 × 103 γ1NV2NA3 transgenic cells. Spleen cells were harvested at different time points and tested in a T cell proliferation assay. Tests were run in triplicate. Values represent the mean stimulation index ± SD of four mice per group (24). The cpm at each time point are as follows: day 5, NVDP peptide (11,581)/medium alone (1,988); day 7, NVDP peptide (40,016)/medium alone (4,932); day 14, NVDP peptide (29,856)/medium alone (1,165); day 21, NVDP peptide (15,788)/medium alone (2,322); and day 28, NVDP peptide (1,014)/medium alone (732). (C) T cell proliferation in lymph nodes (LNs). Fourteen days after injection LNs were collected from the upper, middle, and lower body anatomical regions. The cpm per each group are as follows: upper LN, NVDP peptide (10,576)/NANP peptide (1,201); middle LN, NVDP peptide (10,236)/NANP peptide (1,130); and lower LN, NVDP peptide (9,786)/NANP peptide (887). Spleen cells in the same experiment (data not shown) were NVDP peptide (14,505)/NANP peptide (1,022). (D) Dose-response of CD4 T cell induction. Mice (two per group) were injected with lymphocytes transgenic for γ1NV2NA3 (▪) or γ1NANP (□) as a control, with varying numbers (20,000-70) of transgenic cells. Mice were killed on day 14, and spleen CD4 T cells were restimulated in vitro with the -NVDP- peptide. Proliferation is expressed as cpm. Two independent experiments yielded a similar result. (E) Cytokine production vs. immunizing dose. Culture supernatants from the experiment depicted in D were analyzed for cytokine content (pg/ml). (F) The CD8 T cell response: phase of induction and kinetics after injection of 5 × 103 γ1NV2NP3 transgenic cells. Spleen cells were harvested at the time points indicated, restimulated in vitro with peptide NP366-374 (5 μg/ml), and tested in a standard 51Cr-release assay using EL-4 cells pulsed with NP366-374 as target at various effector-to-target cell ratios. Results are expressed as the percentage of specific lysis. (G) Dose-response of CTL induction. Groups of three mice each received a single injection of varying numbers (20,000-70) of transgenic cells. Mice were killed on day 14, and the CTL response was measured by using EL-4 cells pulsed with NP366-374 (filled symbols) or EL-4 alone (open symbols) as targets.