Table 1.

Phenotypic analysis of B cells infected with rF-TRICOM, activated with CD40L, or infected with rF-TRICOM and activated with CD40L; IFN-γ production by Flu-specific T cells using B cells as APCs






IFN-γ, pg/mL

B7-1
ICAM-1
LFA-3
No peptide
Flu peptide, 0.8 μg/mL
Uninfected   6.9 (21.4)   73.9 (22.0)   79.6 (39.4)   < 15.6   < 15.6  
FP-WT   8.4 (19.2)   71.0 (32.3)   82.7 (40.2)   < 15.6   < 15.6  
CD40L   17.6 (29.8)   86.6 (76.9)   94.3 (86.8)   < 15.6   19.7  
rF-TRICOM   43.1 (51.5)   82.4 (45.1)   73.8 (47.2)   < 15.6   30.5  
CD40L + rF-TRICOM
 
46.7 (66.8)
 
92.0 (90.2)
 
96.0 (92.5)
 
< 15.6
 
59.7
 





IFN-γ, pg/mL

B7-1
ICAM-1
LFA-3
No peptide
Flu peptide, 0.8 μg/mL
Uninfected   6.9 (21.4)   73.9 (22.0)   79.6 (39.4)   < 15.6   < 15.6  
FP-WT   8.4 (19.2)   71.0 (32.3)   82.7 (40.2)   < 15.6   < 15.6  
CD40L   17.6 (29.8)   86.6 (76.9)   94.3 (86.8)   < 15.6   19.7  
rF-TRICOM   43.1 (51.5)   82.4 (45.1)   73.8 (47.2)   < 15.6   30.5  
CD40L + rF-TRICOM
 
46.7 (66.8)
 
92.0 (90.2)
 
96.0 (92.5)
 
< 15.6
 
59.7
 

Numbers in the B7-1, ICAM-1, and LFA-3 columns indicate the percentage of positive cells for each surface marker, and the numbers in parentheses indicate mean fluorescence intensity (MFI). B cells from each treatment were used for stimulation of autologous CD8+ T cells (0.3 × 106/mL); supernatants were tested for IFN-γ production at 24 hours of stimulation. The APC/effector cell ratio used was 1:10.

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