Table 3.

Recognition of CMV-infected fibroblasts after IVS with CMV-poxvirus constructs




Autologous, % lysis

Allogeneic, % lysis
UPN
IVS
CMV infected
Untreated
CMV infected
Untreated
001   pp65/pp150-MVA   40.0   3.5   41.3   2.0  
004   pp65-VV   20.7   0.9   22.4   3.1  
005   UbRpp65-VV   48.4   10.1   NA   NA  
008   UbRpp65-VV   31.0   2.9   27.0   6.0  
009   pp65/pp150-MVA   43.3   7.3   43.8   9.9  
009   IE4-MVA   28.9   0.5   32.8   2.0  
009   pp65/pp150-MVA + IE4-MVA   34.5   7.2   27.4   6.0  
010   UbRpp65/pp150-MVA + IE4-MVA   NA   NA   43.4   15.7  
010   UbRIE4-MVA   NA   NA   30.5   3.3  
011   pp65/pp150-MVA + IE4-MVA   43.8   0.9   46.0   6.4  
011
 
IE4-MVA
 
30.4
 
3.4
 
NA
 
NA
 



Autologous, % lysis

Allogeneic, % lysis
UPN
IVS
CMV infected
Untreated
CMV infected
Untreated
001   pp65/pp150-MVA   40.0   3.5   41.3   2.0  
004   pp65-VV   20.7   0.9   22.4   3.1  
005   UbRpp65-VV   48.4   10.1   NA   NA  
008   UbRpp65-VV   31.0   2.9   27.0   6.0  
009   pp65/pp150-MVA   43.3   7.3   43.8   9.9  
009   IE4-MVA   28.9   0.5   32.8   2.0  
009   pp65/pp150-MVA + IE4-MVA   34.5   7.2   27.4   6.0  
010   UbRpp65/pp150-MVA + IE4-MVA   NA   NA   43.4   15.7  
010   UbRIE4-MVA   NA   NA   30.5   3.3  
011   pp65/pp150-MVA + IE4-MVA   43.8   0.9   46.0   6.4  
011
 
IE4-MVA
 
30.4
 
3.4
 
NA
 
NA
 

Fibroblasts were infected with CMV AD169 and used as targets in CRA as described in “Materials and methods.”

Effectors were PBMC stimulated 7 to 12 days with various CMV-poxvirus constructs, as detailed in “Materials and methods.” The percentage killing of autologous (“Autologous”) and HLA A*0201 (or HLA A*0702 for UPNs 005 and 008) allogeneic (“Allogeneic”) fibroblasts, mismatched at least at 2 other HLA loci are shown at E/T 20 for each donor.

NA indicates that either fibroblasts or effector cells were not available for the assay.

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