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. Author manuscript; available in PMC: 2006 May 30.
Published in final edited form as: J Immunother. 2004;27(1):36–47. doi: 10.1097/00002371-200401000-00004

TABLE 5.

Analysis of g209-2M Peptide-Vaccinated Patient PBMC 1 Year After Immunization

% g209-Specific of CD8+ T Cells* Peptide-Induced Proliferation Cytolytic Activity
Patient Post 4 1 year g280 g209 P g280 g209 P
1 12.4 5.0 11,905 ± 714 18,663 ± 1371 <0.05 62.6 ± 3.4 63.6 ± 4.7 n.s.
2 5.6 0.8 10,208 ± 259 15,069 ± 1809 <0.05 12.0 ± 2.1 11.1 ± 1.5 n.s.
3 6.6 2.0 n.d. n.d. n.d. n.d. n.d. n.d.
5 38.2 25.4 8646 ± 1366 25,259 ± 481 <0.05 13.1 ± 0.8 51.8 ± 1.4 <0.05

Tetramer and functional assays on 1-year postimmunization PBMC were performed concurrently with preimmune and course 4 samples.

*

Values correspond to the number of gated CD8+ tetramer+ cells divided by the number of total CD8bright cells minus the CD8- tetramer+ background (number of CD8- tetramer+ cells divided by total CD8- cell number) × 100.

Values reflect the average counts per minute ± s.e.m. of 3 replicate well cocultures containing 2 × 105 PBMC and an equal number of irradiated T2 cells (20,000 rad) pulsed with 1 μM of g209 or g280 peptide in a 3-day [3H]-thymidine incorporation assay.

Values represent the mean percent lysis from triplicate wells ± s.e.m. at a 100:1 effector to 1 μM peptide-pulsed target cell ratio in a standard 4-hour 51Cr-release assay. Significance values >0.05 are indicated as n.s.