Fig. 5.
Fig. 5. Multiple cell determinants are effectively camouflaged by cell surface derivatization with mPEG. Shown are the scatter plot analyses for CD28 (A) costimulatory molecule present on T cells, binds to CD80; CD3 (B) associated with TCR on T cells and is necessary for signal transduction; CD4 (C) coreceptor for MHC class II molecules present on T cells); and CD80 (D) costimulatory molecule present on B cells and APC. Lane 1 represents the control unmodified PBMC; lane 2 represents the same PBMC population modified with 2.4 mmol/L mPEG (cell concentration of 4 × 106); while lane 3 represents the appropriate isotype control for the sample. In all cases, mPEG modification resulted in a significant decrease (P < .001) in antibody detection of the indicated cell marker. This decrease in antibody detection occurs in a dose-dependent manner upon increasing modification with mPEG (data not shown).

Multiple cell determinants are effectively camouflaged by cell surface derivatization with mPEG. Shown are the scatter plot analyses for CD28 (A) costimulatory molecule present on T cells, binds to CD80; CD3 (B) associated with TCR on T cells and is necessary for signal transduction; CD4 (C) coreceptor for MHC class II molecules present on T cells); and CD80 (D) costimulatory molecule present on B cells and APC. Lane 1 represents the control unmodified PBMC; lane 2 represents the same PBMC population modified with 2.4 mmol/L mPEG (cell concentration of 4 × 106); while lane 3 represents the appropriate isotype control for the sample. In all cases, mPEG modification resulted in a significant decrease (P < .001) in antibody detection of the indicated cell marker. This decrease in antibody detection occurs in a dose-dependent manner upon increasing modification with mPEG (data not shown).

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