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. Author manuscript; available in PMC: 2010 Apr 17.
Published in final edited form as: Cancer Immunol Immunother. 2009 Jun 27;59(1):113–124. doi: 10.1007/s00262-009-0730-7

Fig. 5.

Fig. 5

The Hsd17b12114T and Hsd17b12114–122 peptides have similar affinities for H2-Kd molecules, but only the Hsd17b12114T peptide is recognized by the Meth A-specific CTL. a Binding of the peptides to T2-Kd cells, as defined by mean fluorescence intensity (MFI) of peptide-pulsed cells maintained at 37°C in a MHC stabilization assay using anti-H2-Kd mAb and FITC-conjugated anti-mouse IgG antibody. The MFI of T2-Kd cells alone (asterisk) or pulsed with peptides (plus) and maintained at 4°C are shown. b Cytolytic reactivity of Meth A-specific CTL against T2-Kd cells pulsed with peptides at E/T ratio of 6:1 in 4 h 51Cr-release assays. The Meth A mutant p53232–240 peptide (KYICNSSCM) was used as a negative control peptide