Fig. 1.
Fig. 1. Inhibition of normal B-cell proliferation by rituximab. / (A) Resting tonsillar B cells were stimulated in vitro with SAC (open circles) or anti-μ and anti-CD40 (closed circles) in the presence of the indicated concentrations of rituximab. SAC-stimulated cells were also incubated with a control IgG1 antibody (10 μg/mL My7 IgG1) (open square). 3H-thymidine incorporation of quadruplicate wells was measured at 48 to 66 hours. The data are represented as percentage of the stimulated controls in the absence of rituximab. (B) Resting tonsillar B cells were stimulated with SAC and rituximab was added at 2 μg/mL at the indicated times. 3H-thymidine was measured at 48 to 66 hours.

Inhibition of normal B-cell proliferation by rituximab.

(A) Resting tonsillar B cells were stimulated in vitro with SAC (open circles) or anti-μ and anti-CD40 (closed circles) in the presence of the indicated concentrations of rituximab. SAC-stimulated cells were also incubated with a control IgG1 antibody (10 μg/mL My7 IgG1) (open square). 3H-thymidine incorporation of quadruplicate wells was measured at 48 to 66 hours. The data are represented as percentage of the stimulated controls in the absence of rituximab. (B) Resting tonsillar B cells were stimulated with SAC and rituximab was added at 2 μg/mL at the indicated times. 3H-thymidine was measured at 48 to 66 hours.

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