A simultaneous negative and positive selection method that can detect chimerism at a frequency of 1 per 10,000 by flow cytometry

Tissue Antigens. 1997 Aug;50(2):197-201. doi: 10.1111/j.1399-0039.1997.tb02859.x.

Abstract

A three-color flow cytometric method with a simultaneous negative and positive selection (SNAPS) approach has been developed to detect blood chimerism using a FITC-conjugated recipient-specific HLA monoclonal antibody, a biotinylated donor-specific HLA monoclonal antibody and Cy5-PE-conjugated streptavidin and a PE-conjugated CD3 monoclonal antibody. Detection of simulated blood chimerism at a frequency of 0.01% was achieved by SNAPS. In contrast, by one-color flow cytometry methods, chimerism can be detected at only about 3-4% with the same donor-specific HLA monoclonal antibody. The percentages of donor CD3 cells detected by SNAPS are proportional to the percentages of donor CD3 cells counted. SNAPS method provides a fast, sensitive and reliable way to analyze trace amounts of donor cells in a recipient's blood.

MeSH terms

  • Animals
  • Antibodies, Monoclonal / analysis*
  • Blood Donors
  • CD3 Complex / immunology
  • Chimera / immunology*
  • Flow Cytometry / methods*
  • HLA Antigens / immunology*
  • Humans
  • Immunoglobulin G / analysis
  • Immunoglobulin M / analysis
  • In Situ Hybridization, Fluorescence
  • Lymphocytes / immunology*
  • Mice
  • Sensitivity and Specificity

Substances

  • Antibodies, Monoclonal
  • CD3 Complex
  • HLA Antigens
  • Immunoglobulin G
  • Immunoglobulin M