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. 2003 Jun;109(2):238–245. doi: 10.1046/j.1365-2567.2003.01661.x

Table 1.

Continuous in vivo exposure to ES-62 does not reduce the recovery of splenic B cells or modulate the relative proportions of lymphocyte populations*

Cell type PBS ES-62 (0·05 µg/hr) ES-62 (0·2 µg/hr)
B220 50·2 ± 7·7 42·4 ± 12·0 43·9 ± 10·4
CD3 29·6 ± 1·8 31·5 ± 2·3 31·9 ± 11·4
CD4 21·9 ± 4·7 21·1 ± 8·6 22·7 ± 12·0
CD8 7·7 ± 0·3 8·5 ± 2·0 8·1 ± 1·9
*

Cell counts following sacrifice demonstrated no significant differences in the numbers of cells recovered between PBS and ES-62 treatments and indicated that in vivo exposure to ES-62 did not reduce splenic cellularity. In three experiments using five mice per group, post-death spleen cell counts (mean ± SD) were PBS: 142 ± 38 × 106; ES-62 (0·05 µg/hr): 123 ± 27 × 106 and ES-62 (0·2 µg/hr): 143 ± 7 × 106. Determination of the percentage of individual lymphocyte populations by lineage marker analysis demonstrated that relative cell proportions remained unchanged and that B cell numbers recovered were essentially identical in control and ES-62 treated groups. Data are presented as the percentage of cells (mean ± SD, n = 4 independent experiments) and there were no significant differences amongst any of the groups.