Table 2.

Inverse Targeting of Receptor-Negative Cells in a Mixed Population

Experiment No. EXA (%) SCFXA (%) 4070A (%)
A431  1  <1  50  100  
 2  <1  50 100  
 3  <1  50  100  
TF-1  1  72  92  
 2  20  2  53  
 3  35  6  56 
A431  1  <1  50  100  
 2  <1  50 100  
 3  <1  50  100  
HMC-1  1  61  66  
 2  20  2  29  
 3  29  57 
Experiment No. EXA (%) SCFXA (%) 4070A (%)
A431  1  <1  50  100  
 2  <1  50 100  
 3  <1  50  100  
TF-1  1  72  92  
 2  20  2  53  
 3  35  6  56 
A431  1  <1  50  100  
 2  <1  50 100  
 3  <1  50  100  
HMC-1  1  61  66  
 2  20  2  29  
 3  29  57 

Two milliliters of EXA, SCFXA, or 4070A viral supernatant was used to infect a mixed population of adherent A431 cells (kit-negative, EGF-R–positive) and either HMC-1 or TF-1 suspension cells (kit-positive, EGF-R–negative). After infection, the cells were separated and propagated in their respective media for 72 hours before X-gal staining. Infection with the wild-type control virus gave high titers on both cell types. In contrast, the chimeric vectors could discriminate between cell types. SCFXA vectors preferentially infected the Kit-negative A431 cells, whereas EXA vectors preferentially infected the EGF-R–negative TF-1 or HMC-1 cells. Data showing the individual titers from 3 separate experiments are shown in this table. Titers are shown as percentage blue cells.

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