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. 2012 Jan 31;24(4):233–242. doi: 10.1093/intimm/dxs003

Table 3.

Increased splenic Foxp3+ Treg after depletion of B cells in NOD.H-2h4 mice

Treatmenta Splenocytes (×106)b CD4+ (%) CD4+ (×106) CD4+Foxp3+ (%) Treg/spleen (×106)
Isotype 46.3 ± 0.8 9.6 ± 1.1 4.5 ± 0.7 14.1 ± 0.4 0.62 ± 0.1
Anti-CD20 47.4 ± 0.2 23.2 ± 0.8 10.9 ± 0.6 12.3 ± 0.4 1.36 ± 0.1
Isotype 57.6 ± 0.2 17 ± 0.5 9.8 ± 0.6 10.9 ± 0.8 1.10 ± 0.1
Anti-CD20 52.7 ± 0.2 26.4 ± 1.9 14.1 ± 1.4 11.3 ± 0.7 1.53 ± 0.2
a

Foxp3GFP NOD.H-2h4 mice were given two injections of 125 μg anti-CD20 IgG2a or isotype control at 10 and 16 days of age (lines 1 and 2) or at 6 weeks of age (lines 3 and 4). Foxp3+ Treg in spleens were determined 12 days later, i.e. mice in lines 1 and 2 were 4 weeks old and mice in lines 3 and 4 were almost 8 weeks old. At the time of assay, isotype controls in line 1 had 60.8 ± 1.2% CD19+ B cells compared with 10.5 ± 1.5 in anti-CD20-treated mice and mice in line 3 had 59.4 ± 0.9% CD19+ B cells compared with 18.4 ± 3.1 in age-matched anti-CD20-treated mice (line 4).

b

Mean ± SEM of six to seven mice per group. P < 0.01 for anti-CD20-treated compared with control mice in lines 1 and 2 and P > 0.05 for anti-CD20 compared with controls in lines 3 and 4.