Skip to main content
. Author manuscript; available in PMC: 2008 Feb 10.
Published in final edited form as: J Immunother. 2008 Jan;31(1):1–6. doi: 10.1097/CJI.0b013e31815c193f

FIGURE 3.

FIGURE 3

Persistence of TCR-transduced splenocytes after in vivo transfer. A, (In vitro) Murine C57BL/6 splenocytes were left untransduced (UT), or transduced (TD) with retrovirus encoding the pmel-1 TCR and 24 hours later analyzed by flow cytometry for TCR Vβ13 staining. B, (In vivo) The total number of CD8+gp100 tetramer+ transduced cells was calculated and 1 × 106 or 7 × 106 CD8+ gp 100 tetramer+ cells were transferred into 5 Gy irradiated, B16 tumor bearing C57BL/6 mice with concurrent fowlpox virus expressing hgp 100 vaccination and twice daily IL-2 administration for 3 days. Five days posttransfer, the peripheral blood of mice treated with pmel-1 TCR-transduced splenocytes was analyzed by flow cytometry. The mean fluorescence intensity of Vβ13 expression was as indicated in parentheses. A representative example of the FACS data is shown.