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. Author manuscript; available in PMC: 2013 Jul 24.
Published in final edited form as: Cell Death Differ. 2009 Jan 30;16(5):708–718. doi: 10.1038/cdd.2008.197

Table 3.

Antiapoptotic effects of IRX-2 in comparison to IL-2, IL-7 and IL-15 in MV- or CH-11 Ab-induceda primary T cellsa

CD8+ cells
CD4+ cells
FITC-VAD-FMK+ cells P-valueb FITC-VAD-FMK+ cells P-valueb
(A) MV-induced apoptosis
 Control 21.8±3.9 14.3±5.0
 No IRX-2+MV 71.0±8.0 45.7±1.6 0.0222c
 +IRX-2+MV 20.6±0.8 0.0006 10.2±0.4 0.0038
 +IL-7+MV 49.5±3.5 0.0004 34.5±1.9 0.0124
 +IL-15+MV 16.8±6.2 0.0044 16.7±2.1 0.0072
 +IL-7/IL-15+MV 11.8±6.2 0.0036 11.9±0.8 0.0031
 +IL-2+MV 21.9±2.7 0.0002 22.2±2.7 0.0113
(B) CH-11 Ab-induced apoptosis
 Control 12.3±2.8 11.4±1.3
 No IRX-2+MV 50.0±0.2 46.8±3.0
 +IRX-2+MV 13.4±3.0 0.0007 12.0±1.7 0.0001
 +IL-7+MV 37.7±1.4 0.0015 31.8±10.6
 +IL-15+MV 28.8±3.1 0.0020 21.1±5.3 0.0086
 +IL-7/IL-15+MV 24.2±4.9 0.0028 20.2±0.1 0.0010
 +IL-2+MV 44.2±6.9 31.7±3.0 0.0128
a

Activated primary CD8+ and CD4+ T cells were preincubated with IRX-2 (1 : 3 dilution), recombinant human IL-2 (100 IU/ml), IL-7 (10 ng/ml), IL-15 (10 ng/ml) or IL-7 and IL-15 (both 10 ng/ml) for 24 h and then treated with 10 μg MV or 400 ng/ml CH-11 Ab for an additional 24 h. Activation of caspases was analyzed by flow cytometry. The data are mean percentages of FITC-VAD-FMK+ cells±S.D. obtained in three independent experiments.

b

The P-values refer to significant differences between cells pretreated with IRX-2 compared to MV alone or cells pretreated with the indicated cytokine compared to those pretreated with IRX-2.

c

The P-value refers to the difference in sensitivity to MV-mediated apoptosis between CD8+ and CD4+ T cells