Fig. 8.
Fig. 8. In vivo tracking of BCL1 tumor in the spleen. / HuCD64+ mice received 2 μg murine G-CSF/d subcutaneously 4 days before tumor and continuing throughout the course of therapy (10 days in total). Mice were then inoculated with 107 BCL1 tumor cells intraperitoneally on day 0 and were treated with twice daily injections of 50 μg BsAb intraperitoneally on days 1 to 5 (500 μg/mouse in total). One animal per group was killed on days 5, 10, and 15, and the percentages tumor cells in spleen were determined using flow cytometry with PE-labeled anti-Id versus FITC-labeled anti-CD22. Shown are dot plots from a representative mouse at days 10 and 15, treated with BsAb of the specificities indicated. Control BsAb was the nonbinding [huCD64 × A31 Id].

In vivo tracking of BCL1 tumor in the spleen.

HuCD64+ mice received 2 μg murine G-CSF/d subcutaneously 4 days before tumor and continuing throughout the course of therapy (10 days in total). Mice were then inoculated with 107 BCL1 tumor cells intraperitoneally on day 0 and were treated with twice daily injections of 50 μg BsAb intraperitoneally on days 1 to 5 (500 μg/mouse in total). One animal per group was killed on days 5, 10, and 15, and the percentages tumor cells in spleen were determined using flow cytometry with PE-labeled anti-Id versus FITC-labeled anti-CD22. Shown are dot plots from a representative mouse at days 10 and 15, treated with BsAb of the specificities indicated. Control BsAb was the nonbinding [huCD64 × A31 Id].

Close Modal

or Create an Account

Close Modal
Close Modal