Visualization and Microscopic Quantification of HCMV-Peptide-Specific Cytotoxic T Lymphocytes Using Tetramer Binding

To monitor the frequencies of virus-specific cytotoxic T lymphocytes (CTLs), FACS analyses were performed detecting lymphocyte-specific surface molecules and tetramer binding, as marker for peptide-specificity. Aim of this investigation was to establish an alternative protocol for the quantification...

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Veröffentlicht in:Viral Immunology 2005-09, Vol.18 (3), p.534-538
Hauptverfasser: Bissinger, A.L., Brugger, J., Grigoleit, G.U., Gründemann, C., Hebart, H., Einsele, H., Jahn, G.
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Sprache:eng
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Zusammenfassung:To monitor the frequencies of virus-specific cytotoxic T lymphocytes (CTLs), FACS analyses were performed detecting lymphocyte-specific surface molecules and tetramer binding, as marker for peptide-specificity. Aim of this investigation was to establish an alternative protocol for the quantification of virus-specific CTLs using tetramer binding and microscopic analyzing. The frequencies of HCMV-pp65-peptide-specific CTLs in the blood of eight different HLA-A*0201-positive, HCMV-IgG antibody-positive donors were analyzed with both methods. Using FACS analyses, a median of 0.8% and, using the microscopic analyses, a median of 3.0% was detected in the CD3 + CD8 + cells. After enrichment of HCMV-pp65-peptide-specific CTLs using the interferon-γ secretion assay followed by expansion in cell culture, a median of 90.6% using FACS analyses and a median of 87.1% using the microscopic analyses was detected. Thus, the staining protocol presented in this investigation is an alternative approach to detect and to quantify virus-specific CTLs in low as well as in high frequencies.
ISSN:0882-8245
1557-8976
1365-2567
DOI:10.1089/vim.2005.18.534