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. 1999 May;73(5):3623–3629. doi: 10.1128/jvi.73.5.3623-3629.1999

FIG. 6.

FIG. 6

CD4+ CTL clones lyse HepG2 bystander target cells via a Fas/FasL-mediated mechanism. Clones were incubated with either CMA at 10 nM or BFA at 10 μM for 2 h prior to the addition of target cells. Lysis of labeled HepG2 bystander targets in the presence of unlabeled peptide-presenting BLCL was assessed after an 8-h incubation. The E/T ratio was 10:1. The spontaneous release was ≤27% for all conditions.