Figure 1
Figure 1. In vivo model of lymphoma immunotherapy. Survival of mice given (A) A20 cells, or (B) BL3750 tumor cells from a cMycTG+/− mouse. Left panels: CD20 expression by tumor cells (thick line) and the A20 cell line (thin line) assessed by immunofluorescence staining with flow cytometry analysis. Right panels: Mouse survival following subcutaneous transfer of 106 A20 or 105 BL3750 lymphoma cells on day 0. All mice were given CD20 (•) or control (○) mAb intravenously (250 μg/mouse) on day 1 (n = 4-9 mice/group). (C) Cell surface immunophenotype of BL3750 cells evaluated by immunofluorescence staining with gating on live cells as identified by forward/side light scatter as shown. Comparisons of CD19, CD20, and CD22 expression by BL3750 cells (thick line) and spleen B220+ cells (thin line) from cMycTG+/− mice was assessed by 3-color analysis. Cell surface expression of CD45R (B220), IgM, FcγRIIB, IgD, CD21, CD23, and CD5 (thick line) was assessed by 2-color analysis. Results represent those obtained in 3 independent experiments. (A-C) Background staining using a control (CTRL) mAb is shown (dashed line). (D) Hematoxylin and eosin staining of a lymph node tissue section 28 days after mice were given BL3750 cells. Results represent those obtained in 3 mice. Image was acquired with an Olympus BX60 microscope (Olympus, Center Valley, PA; magnification 40×/1.00 oil iris) and Camera SPOT 1.3.0 (Diagnostic Instruments, Sterling Heights, MI). Image was processed with SPOT 4.0.4 (Diagnostic Instruments) and Adobe Photoshop CS2, version 9.0.2 (Adobe Systems, San Jose, CA).

In vivo model of lymphoma immunotherapy. Survival of mice given (A) A20 cells, or (B) BL3750 tumor cells from a cMycTG+/− mouse. Left panels: CD20 expression by tumor cells (thick line) and the A20 cell line (thin line) assessed by immunofluorescence staining with flow cytometry analysis. Right panels: Mouse survival following subcutaneous transfer of 106 A20 or 105 BL3750 lymphoma cells on day 0. All mice were given CD20 (•) or control (○) mAb intravenously (250 μg/mouse) on day 1 (n = 4-9 mice/group). (C) Cell surface immunophenotype of BL3750 cells evaluated by immunofluorescence staining with gating on live cells as identified by forward/side light scatter as shown. Comparisons of CD19, CD20, and CD22 expression by BL3750 cells (thick line) and spleen B220+ cells (thin line) from cMycTG+/− mice was assessed by 3-color analysis. Cell surface expression of CD45R (B220), IgM, FcγRIIB, IgD, CD21, CD23, and CD5 (thick line) was assessed by 2-color analysis. Results represent those obtained in 3 independent experiments. (A-C) Background staining using a control (CTRL) mAb is shown (dashed line). (D) Hematoxylin and eosin staining of a lymph node tissue section 28 days after mice were given BL3750 cells. Results represent those obtained in 3 mice. Image was acquired with an Olympus BX60 microscope (Olympus, Center Valley, PA; magnification 40×/1.00 oil iris) and Camera SPOT 1.3.0 (Diagnostic Instruments, Sterling Heights, MI). Image was processed with SPOT 4.0.4 (Diagnostic Instruments) and Adobe Photoshop CS2, version 9.0.2 (Adobe Systems, San Jose, CA).

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