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. 2007 Dec;150(3):397–406. doi: 10.1111/j.1365-2249.2007.03496.x

Table 1.

Effects of immunoglobulin G (IgG) on the expression of cell surface molecules in healthy controls.

Day 7 Day 9


Molecule Monocyte IgG Saline IgG Saline
CD1a 6·9 ± 4·3 59·8 ± 12·0** 74·5 ± 9·3 64·4 ± 8·5** 79·5 ± 8·0
CD83 3·7 ± 2·6 20·9 ± 8·7** 14·3 ± 9·0 50·1 ± 6·6** 29·7 ± 2·8
CD40 3·9 ± 2·3 34·0 ± 9·7 34·4 ± 10·3 53·9 ± 13·0** 81·0 ± 8·7
CD80 0·8 ± 0·8 25·4 ± 8·2* 32·3 ± 9·5 48·9 ± 14·1** 81·4 ± 7·2
CD86 78·0 ± 14·2 74·3 ± 13·2** 51·5 ± 17·5 96·8 ± 3·0* 84·7 ± 15·5
HLA-DR 46·0 ± 19·5 21·4 ± 11·9 21·1 ± 12·2 52·6 ± 24·0 48·1 ± 22·3
CD49d 94·4 ± 3·4 39·7 ± 8·2** 29·5 ± 8·7 27·5 ± 10·9** 49·8 ± 12·3

Monocyte isolation and differentiation into DCs were performed as described in Materials and methods. Healthy control samples (n = 8) were each divided into a group with IgG added at the beginning of the culture period (IgG) and a group treated with vehicle alone (saline). Monocytes and cells on days 7 and 9 of treatment were analysed by flow cytometry. The results show the frequency of cells (%) positive for each cell surface molecule [CD1a, CD83, CD40, CD80, CD86, human leucocyte antigen D-related (HLA-DR), and CD49d] as the mean value ± standard deviation. To calibrate the differences between the paired mean values, we used a paired t-test

**

(P < 0·01

*

P < 0·05).