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. 1997 Jul 22;94(15):8070–8075. doi: 10.1073/pnas.94.15.8070

Table 1.

Efficiencies of CD8+ CD44low LN T cell cloning and cytokine mRNA detection among subclones

Parameter Experiment 1 Experiment 2 Experiment 3 Experiment 4
Primary cultures
No. parent cells cultured 480 480 180 300
% cultures with ≥1 cell at day 2  72%  75%  59%  58%
% cultures with ≥2 cells at day 2  69%  62%  46%  52%
Secondary cultures IL-2 IL-2 + IL-4 IL-2 IL-2 + IL-4 IL-2 IL-2 + IL-4 IL-2 IL-2 + IL-4
No. cells transferred on day 2 78 75 58 56 68 60 58 51
% cells that recloned by day 5 83% 75% 95% 88% 85% 75% 88% 84%
Mean subclone size on day 5 52 ± 38 38 ± 32 66 ± 49 43 ± 40 106 ± 70 86 ± 69 130 ± 63 106 ± 54
No. subclones assayed by RT-PCR 55 (38) 54 (38) 44 (37) 44 (37) 42 (38) 44 (38) 30 (30) 30 (30)
No. β-actin/CD3ɛ+ subclones 37 (26) 35 (26) 25 (25) 20 (18) 42 (38) 44 (38) 30 (30) 30 (30)
No. informative parent cells  20  13  38  30

Numbers in parentheses indicate the number of parent cells from which the assayed subclones were derived.