Figure 5.
Figure 5. HLA restriction of peptide recognition by HM1.24-specific CTL line. CTL line specific for HM1.24-165 peptide was established from a healthy donor (HLA-A2+, A24-). (A) HLA restriction of HM1.24-165–induced CTLs was determined by blocking HLA class I on target cells. 51Cr-labeled target ARH-77 cells were preincubated with either control MoAb or anti–HLA class I MoAb for 45 minutes at room temperature before addition of the CTLs. Cytotoxicity (%) was measured by 51Cr-release assay (E/T ratio = 20). (B) Peptide recognition by the CTLs was determined by cold target inhibition assay. CTLs (6 × 104 cells) were incubated with 51Cr-labeled target ARH-77 cells (3 × 103 cells) in the presence of either HM1.24-165 peptide-loaded or unloaded MDA-MB-231 cells (6 × 104 cells). Cytotoxic activity was measured by 51Cr-release assay (E/T ratio = 20). Values indicate the mean ± SD of triplicate experiments.

HLA restriction of peptide recognition by HM1.24-specific CTL line. CTL line specific for HM1.24-165 peptide was established from a healthy donor (HLA-A2+, A24-). (A) HLA restriction of HM1.24-165–induced CTLs was determined by blocking HLA class I on target cells. 51Cr-labeled target ARH-77 cells were preincubated with either control MoAb or anti–HLA class I MoAb for 45 minutes at room temperature before addition of the CTLs. Cytotoxicity (%) was measured by 51Cr-release assay (E/T ratio = 20). (B) Peptide recognition by the CTLs was determined by cold target inhibition assay. CTLs (6 × 104 cells) were incubated with 51Cr-labeled target ARH-77 cells (3 × 103 cells) in the presence of either HM1.24-165 peptide-loaded or unloaded MDA-MB-231 cells (6 × 104 cells). Cytotoxic activity was measured by 51Cr-release assay (E/T ratio = 20). Values indicate the mean ± SD of triplicate experiments.

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