Table 5.

Humoral immune responses to recipient-derived leukemic blasts before and after immunization



Anti-human IgG avidin PE, MFI
Pt/dosage*
Before study
After 3 injections
After 6 injections
Control
2/1   628   601   744   640  
3/1   41   59   67   55  
4/1   70   74   101   83  
6/2   261   385   516   85  
7/2   24   31   58   16  
8/3   4   4   4   NA  
9/3
 
292
 
341
 
309
 
270
 


Anti-human IgG avidin PE, MFI
Pt/dosage*
Before study
After 3 injections
After 6 injections
Control
2/1   628   601   744   640  
3/1   41   59   67   55  
4/1   70   74   101   83  
6/2   261   385   516   85  
7/2   24   31   58   16  
8/3   4   4   4   NA  
9/3
 
292
 
341
 
309
 
270
 

Differences in MFI were not statistically significant between patients (P > .091). Patients 6 and 7 had a 2- to 3-fold increase of their postimmunization MFI compared with healthy controls. Patient 1 (dose level 1) experienced early disease progression. Patients 5 (dose level 2) and 10 (dose level 3) did not have enough blasts for immunologic studies.

PE indicates phycoerythrin; MFI, mean fluorescence intensity; and NA, not available.

*

The dose-escalation schedule began at 2 × 105 CD40L-secreting skin fibroblasts per injection (dose level 1), increasing in log increments to 2 × 107 (dose level 3). IL-2-secreting skin fibroblasts and recipient-derived blasts were administered at a fixed dosage throughout the study (2 × 107 per injection)

Controls consisted of pooled plasmas from healthy donors; not shown are the responses of the patients' plasmas against unrelated cells (no increase in the fluorescent signal)

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