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. 2003 Jan;131(1):82–89. doi: 10.1046/j.1365-2249.2003.02047.x

Fig 5.

Fig 5

Antibody blocking of cytotoxicity assay. Effectors from one patient were cultured alone (Inline graphic), with autologous DCs pulsed with lysate (□) or lysate buffer (Inline graphic), with autologous DCs electrofused with B-CLL B cells (▪) and with autologous DCs mixed with B-CLL B cells (Inline graphic). Anti-CD4 and anti-CD8 monoclonal antibodies were added to effectors incubated with autologous B-CLL B cell targets at an effector : target ratio of 40 : 1. Specific cytotoxicity to B-CLL targets, by T cell effectors generated from culture with lysate-pulsed autologous DCs, was significantly inhibited by anti-CD4 (P = 0·039) but not by anti-CD8 monoclonal antibodies. However, specific cytotoxicity by T cell effectors generated from culture with autologous DC–B-CLL hybrids was inhibited by anti-CD4 (P = 0·062) and inhibited significantly by anti-CD8 (P = 0·018) monoclonal antibodies. Each treatment group was measured in duplicate. Data were analysed by unpaired Students' t-test; *P = 0·039, **P = 0·062, ***P = 0·018.