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. 2004 Mar;135(3):398–408. doi: 10.1111/j.1365-2249.2003.02380.x

Table 2.

CD4+ CD25+ LNC of SADBE-treated AA mice display weak inhibitory potential

cpm/1 × 105 or 1·5 × 105 cellsa (% inhibition)b

LNC Subpopulation Stimulus Healthy AA SADBE-treated AAc
Unseparated ConA 14·244 9·706 14·009
CD4+ CD25 ConA 10·713 8·180 11·012
CD4+ CD25+ ConA  7·215 7·244 12·410
Unseparated + CD4+ CD25+ ConA  7·593 (57·5) 7·972 (40·2) 16·189 (20·0)
CD4+ CD25- + CD4+ CD25+ ConA  7·309 (49·0) 9·288 (21·3) 16·389 (4·8)
Unseparated anti-CD3 35·282 nt 22·680
CD4+ CD25- anti-CD3 31·220 nt 27·955
CD+ CD25+ anti-CD3  4·868 nt 22·717
Unseparated + CD4+ CD25+ anti-CD3 10·392 (72·4) nt 29·398 (13·6)
CD4+ CD25 + CD4+ CD25+ anti-CD3  6·408 (81·0) nt 34·904 (11·2)
a

Counts per minute (cpm) are derived from 1 × 105 unseparated, CD4+ CD25- and CD4+ CD25+ lymphocytes and from 1 × 105 unseparated plus 0·5 × 105 CD4+ CD25+ and 1 × 105 CD4+ CD25 plus 0·5 × 105 CD4+ CD25+ lymphocytes, respectively; s.d. of triplicates were in the range of 2–5% and are not shown for clarity of presentation.

b

% Inhibition has been calculated from the sum of cpm obtained with the individual populations.

c

Mice were treated weekly with 0·5–1% SADBE in acetone for 8–12 weeks.