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Abstract Proliferation of human lymphocytes in response to various stimuli has traditionally been assessed by measuring uptake of radiolabeled nucleotides such as 3 H‐thymidine. We have evaluated a fluorometric assay, which uses the commercially available reagent, alamarBlue, as a potential substitute for the 3 H‐thymidine assay in measuring proliferation of human lymphocytes. In this assay, alamarBlue TM is added to a population of cells where it is reduced by mitochondrial enzyme activity. The reduced form of the reagent is fluorescent and can be quantitatively detected. The safety and convenience of the alamarBlue TM assay make it very attractive for use in the clinical laboratory. In this study peripheral blood mononuclear cells (PBMC) from healthy donors were stimulated using the mitogen Concanavalin A, and proliferation was assessed using either the 3 H‐thymidine or the alamarBlue TM assay. The alamarBlue TM assay reliably detects human PBMC and we found that the linear range of detection was 10 4 cells/well (96‐well plate) to 5 × 10 5 cells/well. Detection of human PBMC is highly reproducible and the alamarBlue assay may be suitable in a number of applications where detection or relative quantitation of human PBMC is required. The alamarBlue assay also detected mitogen induced proliferation of PBMC although with a significantly lower level of sensitivity than the standard 3 H‐thymidine assay.©1995 wiley‐Liss, inc.
Fries et al. (Sun,) studied this question.