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. 2008 Aug;19(8):1520–1529. doi: 10.1681/ASN.2007121375

Table 1.

Systemic inflammatory response of mice from groups 1 and 2a

Characteristics of Mice Group 1
Group 2
Vehicle Rapamycin Vehicle Rapamycin
Cytokine expression in LN
    IFN-γ 53.7 ± 9.2 14.9 ± 3.8b 36.8 ± 7.9 22.0 ± 5.5
    TNF-α 4.2 ± 0.5 3.0 ± 0.4 5.1 ± 1.0 5.9 ± 0.8
    IL-6 23.6 ± 18.9 1.5 ± 0.4 20.8 ± 5.6 21.9 ± 6.8
    IL-10 3.3 ± 0.3 2.9 ± 0.4 6.9 ± 1.2 6.0 ± 0.8
    IL-17 10.1 ± 1.3 4.6 ± 1.3b 13.7 ± 3.5 15.1 ± 4.0
FoxP3 expression in LN 5.7 ± 1.1 4.9 ± 0.7 7.2 ± 2.7 4.8 ± 1.2
Splenocyte proliferation
    proliferation to LPS (OD 450) 0.50 ± 0.00 0.22 ± 0.00b 1.81 ± 0.10 1.92 ± 0.20
    proliferation to PHA (OD 450) 0.48 ± 0.00 0.21 ± 0.00b 2.12 ± 0.20 2.00 ± 0.20
B cell response
    rabbit anti-mouse IgG (OD 450) 0.73 ± 0.10 0.34 ± 0.10b 0.91 ± 0.10 0.73 ± 0.10
Deposition of rabbit IgG (titer) 1:3200 1:3200 1:3200 1:3200
a

Mice were treated with either rapamycin or vehicle starting on the day of immunization (group 1; n = 8 in the rapamycin group, n = 6 in the vehicle group) or 14 d after induction of anti-GBM GN (group 2; n = 8 per group). We evaluated the cytokine expression profiles and FoxP3 expression in the lymph node (LN), splenocyte proliferation, and the amount of mouse anti-rabbit IgG in the serum 21 (group 1) or 35 d (group 2) after induction of anti-GBM GN. In addition we provided the titer of the deposited rabbit IgG on the GBM. The cytokine expressions evaluated by real-time PCR are given as fold increase compared with healthy controls. Data are means ± SEM.

b

P < 0.05 versus the respective control group.