Fig. 2.
Fig. 2. RIT of BCL1 using radioiodinated and unlabeled anti-B cell MoAb. (A) Composite graph showing results from three individual RIT (minimum of 40 animals per group) performed under the same experimental conditions. Mice were given 106 fresh BCL1 cells IV on day 0 and then treated with MoAb (500 μg with or without approximately 5 MBq 131I) 4 days later. (B) Groups of 10 BCL1-bearing mice were treated as in Fig 2A, but with 750 μg of MoAb (with or without approximately 7.5 MBq of131I) on day 4. Treatments included: Control IgG (⋆);131I-control IgG (⧫); anti-MHCII (TI2-3; ○, •); anti-Id (□, ▪); anti-CD19 (⌓;); anti-CD22 (▵, ▴); and anti-MHCII MoAb (N22; ▿, ▾). The solid and open symbols represent MoAb labeled with and without radioactive iodine, respectively. Results with the anti-MHCII MoAb (○, •) are shown in both (A) and (B). Animal survival was monitored daily. Control 131I-IgG1 MoAb had a very small, but statistically significant therapeutic effect (P < .01).

RIT of BCL1 using radioiodinated and unlabeled anti-B cell MoAb. (A) Composite graph showing results from three individual RIT (minimum of 40 animals per group) performed under the same experimental conditions. Mice were given 106 fresh BCL1 cells IV on day 0 and then treated with MoAb (500 μg with or without approximately 5 MBq 131I) 4 days later. (B) Groups of 10 BCL1-bearing mice were treated as in Fig 2A, but with 750 μg of MoAb (with or without approximately 7.5 MBq of131I) on day 4. Treatments included: Control IgG (⋆);131I-control IgG (⧫); anti-MHCII (TI2-3; ○, •); anti-Id (□, ▪); anti-CD19 (⌓;); anti-CD22 (▵, ▴); and anti-MHCII MoAb (N22; ▿, ▾). The solid and open symbols represent MoAb labeled with and without radioactive iodine, respectively. Results with the anti-MHCII MoAb (○, •) are shown in both (A) and (B). Animal survival was monitored daily. Control 131I-IgG1 MoAb had a very small, but statistically significant therapeutic effect (P < .01).

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