Fig. 1.
Fig. 1. CDC activity and binding levels of various antibodies directed to the B-cell surface. / (A) CDC induced by a panel of mouse IgG1 and IgG2a isotype mAbs directed at CD20, CD37, CD38, and MHCII. Daudi (▪) or EHRB (▨) cells (1 × 106/mL) were incubated with mAbs (10 μg/mL) for 15 minutes at room temperature. Normal human serum (NHS, 20% vol/vol) was then added as a source of complement and the cells incubated at 37°C for 30 minutes. Cell lysis was assessed by flow cytometry using a PI exclusion assay, and the level of CDC expressed as PI-positive cells as a percentage of total cells. The results show the means and SDs of 3 separate experiments. (B) Surface expression of CD20, CD37, CD38, and MHCII antigens on Daudi or EHRB cells. Daudi or EHRB cells (5 × 105/mL) were incubated with mAbs (10 μg/mL) for 30 minutes at room temperature, then washed and incubated with goat anti–mouse IgG F(ab′)2 FITC for 30 minutes on ice, prior to washing and analysis by flow cytometry.

CDC activity and binding levels of various antibodies directed to the B-cell surface.

(A) CDC induced by a panel of mouse IgG1 and IgG2a isotype mAbs directed at CD20, CD37, CD38, and MHCII. Daudi (▪) or EHRB (▨) cells (1 × 106/mL) were incubated with mAbs (10 μg/mL) for 15 minutes at room temperature. Normal human serum (NHS, 20% vol/vol) was then added as a source of complement and the cells incubated at 37°C for 30 minutes. Cell lysis was assessed by flow cytometry using a PI exclusion assay, and the level of CDC expressed as PI-positive cells as a percentage of total cells. The results show the means and SDs of 3 separate experiments. (B) Surface expression of CD20, CD37, CD38, and MHCII antigens on Daudi or EHRB cells. Daudi or EHRB cells (5 × 105/mL) were incubated with mAbs (10 μg/mL) for 30 minutes at room temperature, then washed and incubated with goat anti–mouse IgG F(ab′)2 FITC for 30 minutes on ice, prior to washing and analysis by flow cytometry.

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