Table 2.

Cytolytic characteristics of HATGF-βRII-Δcyt–transduced versus nontransduced cytotoxic T-lymphocyte lines with and without exposure to exogenous transforming growth factor β

CTL line% Specific lysis (ratio 10:1)Day of culture* (d after transduction)
NontransducedTGF-βRII-Δcyt transduced
Auto LCLAuto LCL + TGF-βAuto LCLAuto LCL + TGF-β
Patient 1 69 27 63 66 70  (21) 
Patient 2 43 18 40 41 96  (14)  
Patient 3 41 24 30 35 88  (26)  
Patient 4 26 27 23 120  (21)  
Donor 1 37 19 44 54 42  (26)  
Donor 2 95 69 44 53 56  (21)  
Donor 3 64 54 48 42 52  (14)  
Donor 4 61 36 22 23 52  (14) 
CTL line% Specific lysis (ratio 10:1)Day of culture* (d after transduction)
NontransducedTGF-βRII-Δcyt transduced
Auto LCLAuto LCL + TGF-βAuto LCLAuto LCL + TGF-β
Patient 1 69 27 63 66 70  (21) 
Patient 2 43 18 40 41 96  (14)  
Patient 3 41 24 30 35 88  (26)  
Patient 4 26 27 23 120  (21)  
Donor 1 37 19 44 54 42  (26)  
Donor 2 95 69 44 53 56  (21)  
Donor 3 64 54 48 42 52  (14)  
Donor 4 61 36 22 23 52  (14) 

Percentage of specific 51Cr release was determined after 4-hour coincubation with autologous lymphoblastoid cell line (LCL) in cytotoxic T-lymphocyte (CTL) lines with and without transforming growth factor β (TGF-β) added to CTL cultures 96 hours before the cytotoxicity assay. The table shows the percentage of specific lysis at an effector-to-target ratio of 10:1 in the CTL lines generated from 4 healthy donors and 4 patients with Hodgkin disease. The far right column shows the day of CTL culture/and day after transduction when the cytotoxicity assay was performed.

*

Cytotoxicity of transduced and nontransduced CTLs was tested on the same day of culture.

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