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. Author manuscript; available in PMC: 2013 Apr 1.
Published in final edited form as: Nat Immunol. 2012 Sep 9;13(10):991–999. doi: 10.1038/ni.2416

Table 1.

Induction of EAE following adoptive transfer of MOG specific TH17 cells and active immunization.

Mice Groups Disease
incidence
(%)
Mean
score α
Mean
day of
onsetα
Mortality
(%)
Statistics
2D2 IL-1β+IL-6+IL-23 20/21 (95%) 3.7±0.29 12.2±0.35 10/21 (48%) ns
2D2 TGF-β3+IL-6 13/15 (86%) 3.5±0.35 12.7±0.92 4/15 (26%) p<0.001
2D2 TGF-β1+IL-6 10/17 (58%) 2.6±0.45 14.1±1.77 0/17 (0%)
2D2 TGF-β1+IL-6+IL-23 11/21 (52%) 3.6±1.53 14.8±2.40 5/21 (23%) p<0.001χ
2D2xIL-23R−/− IL-1β+IL-6+IL-23 0/8 (0%) n/a n/a 0/8 (0%) p<0.001β
2D2xIL-23R−/− TGF-β3+IL-6 0/8 (0%) n/a n/a 0/8 (0%) p<0.001β
Wt Isotype control 19/22 (86%) 2.4±0.25 9±0.83 0/22 (0%) p<0.001
Wt Anti-TGF-β3 710 (70%) 1.6±0.37 9.8±2.2 0/10 (0%)
2D2xTbx21−/− TGF-β3+IL-6 8/11 (73%) 2.8±1.13 18.9±4.58 1/11 (1%) p<0.001
2D2xTbx21 TGF-β1+IL-6 0/11 (0%) n/a n/a 0/11 (0%)
2D2xTbx21 TGF-β1+IL-6+IL-23 0/7 (0%) n/a n/a 0/7 (0%) p<0.001β

The transferred 2D2 CD4+ cells were cultured in the presence of various combinations of IL-23, TGF-β, IL-1β, and IL-6.

Active EAE was induced with MOG35-55/CFA plus pertussis toxin.

Disease incidence, mean day of onset, and mortality are reported as number of mice affected/total number of mice

α

Mean calculated only from mice that developed clinical signs of experimental autoimmune encephaltomyelitis.

β

Compared to 2D2 controls with indicated cytokine conditions

χ

Compared to 2D2 (TGF-β1+IL-6+IL-23) to 2D2 (TGF-β1+IL-6) conditions

n/a : Denotes: not applicable

ns: Denotes: not significant