Skip to main content
. 2015 Sep 7;6(31):31344–31359. doi: 10.18632/oncotarget.5181

Table 3. Infection of human DCs with Tri-Ad5 can generate brachyury-, MUC1- and CEA-specific CTLs that efficiently lyse tumor cells expressing all three antigens.

Antigen-specific T-cell lines SW620 Brachyury+ MUC1+ CEA+ (HLA-A2+/A24+) ASPC-1 Brachyury+ MUC1+ CEA+ (HLA-A1+/A26+)
T-brachyury 64.4 (3.6) 8.3 (2.7)
T-MUC1 (P93L) 28.5 (1.3) 2.0 (1.6)
T-MUC1 (C6A) 49.3 (3.3) 5.0 (1.8)
T-CEA 42.4 (3.7) 4.3 (1.9)

Human dendritic cells (DCs) were infected with Tri-Ad5 at 20, 000 MOI. Infected DCs were used to generate specific cytotoxic T lymphocytes (CTLs) using autologous peripheral blood monoclonal cells (PBMCs). Autologous DCs were used as antigen-presenting cells for three in vitro stimulations (IVS). Autologous peptide-pulsed B cells were used to re-stimulate antigen-specific CTLs for two additional IVS. The effector-to-target ratio used was 30:1; CTLs were used at IVS 5. Results are expressed in % specific lysis (SD).