Mounting evidence for the clinical significance of the CD 14(weak) CD 16(st
rong) monocyte subpopulation in peripheral blood induced the demand for an
efficient method for its determination. We propose a simple, fast, no-wash
now cytometric method using fluorescence-labelled anti-CD14, anti-CD16, and
anti-HLA-DR antibodies and ammonium chloride-based erythrocyte lysis. This
type of analysis can be performed on a standard three-colour flow cytomete
r. The method avoids interference by NK-cells and neutrophil granulocytes w
ithout defining monocytes by stringent light scatter criteria that might le
ad to a loss of CD14(weak) CD16(strong) monocytes. It, therefore, offers hi
gh reliability and accuracy Its performance recommends the method to be use
d for routine clinical measurements of CD14(weak) CD16(strong) monocytes.