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. 2013 Oct 6;174(2):281–291. doi: 10.1111/cei.12165

Table 1.

Cytokine production from activated γδ and CD4+ T cells

Cytokine concentration (pg/ml) Cytokine concentration (pg/ml)


Resting γδ Activated γδ P n Resting CD4 Activated CD4 P n
IFN-γ 21·8 ± 8·0 1124·6 ± 513·3 <0·001 10 3·0 ± 2·2 1605·1 ± 423·9 <0·001 8
IL-4 3·8 ± 1·6 10·0 ± 2·6 n.s. 8 3·0 ± 1·8 107·6 ± 37·9 <0·001 8
IL-10 5·5 ± 0·9 30·7 ± 8·1 <0·05 9 2·5 ± 1·3 630·5 ± 173·9 <0·001 8
TNF-α 33·4 ± 8·5 1050·4 ± 256·9 <0·001 10 4·4 ± 2·1 2630·1 ± 440·4 <0·001 8
IL-1β 12·6 ± 2·8 54·9 ± 11·9 <0·05 6 2·4 ± 0·8 68·4 ± 21·8 <0·05 6
IL-6 151·7 ± 33·3 430·1 ± 131·1 <0·05 10 14·2 ± 4·4 327·6 ± 94·3 <0·05 8
IL-17 4·3 ± 4·2 13·5 ± 10·9 n.s. 16 9·7 ± 9·7 354·6 ± 118·5 <0·001 14
GM-CSF 0·7 ± 0·4 209·1 ± 60·9 <0·05 3 n.d. 4412·5 ± 1575·9 3

The production of pro- and anti-osteoclastogenic cytokines was determined for resting γδ and CD4 T cells, and following anti-CD3/anti-CD28 stimulation for 24 h. Production of interferon (IFN)-γ, interleukin (IL)-10, tumour necrosis factor (TNF)-α, IL-1β, IL-6 and granulocyte– macrophage colony-stimulating factor (GM-CSF) was assessed using a multiplexed cytometric bead array. IL-17 production was assessed by enzyme-linked immunosorbent assay (ELISA). Data shown are mean ± standard error of the mean from independent experiments from n number of independent donors (n.s. = not significant; n.d. = not determined).