The soluble anti-CD3 antibodies had no effect on T-cell proliferation (data not shown). In addition, neither the scFv anti-CD33 by itself nor any of the fusion proteins carrying the costimulatory molecules was able to induce proliferation (Fig. 1). Suboptimal T-cell proliferation was observed at concentrations smaller than 5 μg/ml dscFv anti-CD33/anti-CD3. The combination of 10 μg/ml sc CD80/anti-CD33 fusion protein with

the suboptimal concentration of 2 μg/ml AZD1208 supplier dscFv anti-CD33/anti-CD3 did not significantly enhance T-cell proliferation above that seen with dscFv anti-CD33/anti-CD3 alone (Fig. 2a). In contrast, T-cell proliferation was significantly increased by the combination of 2 μg/ml dscFv anti-CD33/anti-CD3 and 10 μg/ml sc CD86/anti-CD33 (P < 0·05) and reached levels that were comparable with the higher doses of dscFv anti-CD33/anti-CD3 (10 μg/ml). Another functionally important T-cell activation parameter is their ability to kill target cells. In agreement with the proliferation data, concentrations of dscFv anti-CD33/anti-CD3 smaller than 5 μg/ml induced a suboptimal level of T-cell cytotoxicity when compared with 10 μg/ml dscFv Daporinad mouse anti-CD33/anti-CD3.

However, the level of cytotoxicity could be significantly enhanced by adding 10 μg/ml sc CD86/anti-CD33 to 2 μg/ml dscFv anti-CD33/anti-CD3 (Fig. 2b). Under these conditions cytotoxicity levels were almost identical to the levels achieved with 10 μg/ml dscFv anti-CD33/anti-CD3. Only a small and insignificant increase in T-cell cytotoxic activity could be observed when 10 μg/ml sc CD80/anti-CD33 fusion protein was added to 2 μg/ml dscFv anti-CD33/anti-CD3. This difference between CD86 and CD80 costimulation was not only restricted to the single dose of 10 μg/ml but was also seen over an entire dose range (0·01–10 μg/ml; data not shown). The magnitude of Ca2+ influx has been shown to correlate

with T-cell proliferation23,28 so we tested the hypothesis that differences in Ca2+ signalling are responsible for differences in T-cell activation observed during costimulation. To analyse Ca2+ signals in single cells following costimulation, we established conditions that allowed Loperamide us to measure Ca2+ signals in primary T cells following stimulation by bi-specific antibody-loaded CHO cells (Fig. 3a). Contact between T cells and CHO cells that were preloaded with dscFv anti-CD33/anti-CD3 (used at 2 μg/ml from now on) induced Ca2+ signals in almost all cells, whereas cells with no contact showed no Ca2+ signals. The ratio 340/380, which is proportional to [Ca2+]i, is shown over time for one T cell that makes a CHO-cell contact and one T cell that makes no CHO-cell contact (Fig. 3b). We observed [Ca2+]i rises only in cells with contact, but not in cells with no contact or in cases when only costimulatory antibodies were used (Fig. S3).