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. 2000 May;74(9):4093–4101. doi: 10.1128/jvi.74.9.4093-4101.2000

FIG. 4.

FIG. 4

Virus-infected DC and Mφ process and present the immunodominant antipolyomavirus CTL epitope. (A) Uninfected, MT389-397 peptide-pulsed or virus-infected thioglycolate-elicited Mφ or FACS-sorted CD11c+ DC were cocultured with the MT389-397-specific T-cell hybridoma H8-1.18 for 24 h, and IL-2 levels measured by determining [3H]thymidine incorporation by CTLL cells. Splenic CD11c+ DC were also FACS sorted at day 2 postinfection and assayed for their capacity to stimulate H8-1.18. Stimulators: ■, uninfected; ⧫, in vitro infected; ●, MT389-397 pulsed; ▴, in vivo infected. (B) DC (5 × 104/well) pulsed with heat-inactivated (HI) virus, pulsed with MT389-397 peptide, infected by polyomavirus, or left untreated were cultured for 24 h with H8-1.18 cells, and IL-2 production was measured by CTLL bioassay.