Interference in microsphere flow cytometric multiplexed immunoassays for human cytokine estimation

Donald J. Phillips, Stacy C. League, Paula Weinstein, W. Craig Hooper

Research output: Contribution to journalArticle

11 Scopus citations

Abstract

The present study describes positive and negative interference of human cytokine measurement in multiplexed bead-based immunoassays. Significant differences in measured IL-6 and TNF-α values in 30 normal human plasma samples were apparent depending on whether measurements were with a 2-plex assay or embedded in a multiplex of 8-or more cytokine antibody pairs, as well as among the kits of 3-different vendors. Sample diluents containing proprietary blocking ingredients were shown to greatly affect the outcome of measured cytokine values. Additionally, recovery of IL-6 and TNF-α from spiked samples suggests significant negative interference from either endogenous antibodies, soluble receptors or anti-cytokine antibodies in 10% and 26% of samples, respectively. While it is evident that multiplexed immunoassays hold great promise for cytokine profiling, there are still important issues needing further study. Especially needed are universally optimized sample diluents, uniformly calibrated standards with mass values, and internal assay controls, which should greatly facilitate intralaboratory accuracy and precision and interlaboratory comparisons of cytokine measurements. Possible causes of interference and remedies are discussed.

Original languageEnglish (US)
Pages (from-to)180-188
Number of pages9
JournalCytokine
Volume36
Issue number3-4
DOIs
StatePublished - Nov 1 2006
Externally publishedYes

Keywords

  • Cytokines
  • Heterophile antibody
  • IgY
  • Immunoassay interference
  • Microspheres
  • Multiplexed assay

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology
  • Biochemistry
  • Hematology
  • Molecular Biology

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