Natural Killer Cell Cytotoxicity: A Methods Analysis of Versus Flow Cytometry Chromium Release

Author:

Motzer Sandra Adams1,Tsuji Joyce2,Hertig Vicky3,Johnston Sandra K.4,Scanlan James5

Affiliation:

1. Department of Biobehavioral Nursing and Health Systems, Box 357266, University of Washington, Seattle, WA 98195-7266,

2. Biobehavioral Immune Laboratory

3. “NK Cell Activity and IBS Across the Menstrual Cycle”

4. “NK Cell Activity and IBS Across the Menstrual Cycle” in the Department of Biobehavioral Nursing and Health Systems, School of Nursing, University of Washington, Seattle

5. School of Medicine, Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle

Abstract

The purpose of this study is to describe design considerations for the use of flow cytometry (FC) com-pared to51 chromium (51 Cr)-release assays utilizing cryopreserved peripheral blood mononuclear cells (PBMCs) to detect natural killer (NK) cell cytotoxicity. Subjects were 10 healthy women aged 18 to 39 years. Intra-assay variability between methods differed only at the lowest effector-target ratios evaluated. Interassay variability was wide but did not differ between methods. The relationship of lytic unit-10 between methods was strongly positive. Cytotoxicity detected by51 Cr release was higher than that detected by FC for all 10 subjects. Cost was comparable. How-ever, had more assays been performed, technician time would have been greater with flow cytometry. More whole blood was needed to perform the flow cytometry cytotoxicity assay than51 Cr-release cytotoxicity assay. The authors found no compelling reason to adopt NK cell cytotoxicity by flow cytometry over51 Cr release.

Publisher

SAGE Publications

Subject

Research and Theory

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