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A comparison of electrochemiluminescence and flow cytometry for the detection of natural latex-specific human immunoglobulin E.

Abstract
In vitro correlates of type 1 hypersensitivity to natural latex (NL) proteins continue to be limited by both sensitivity and specificity. Methods which have detection limits in the picogram range, namely, radioallergosorbent assays (RAST) and enzyme-linked immunosorbent assays (ELISA), are inadequate for the identification of NL hypersensitivity in certain at-risk groups, such as health care workers. A flow cytometry assay (FCA), previously shown to be comparable to RAST and ELISA in the identification of NL-sensitized pediatric patients with spina bifida, was compared with electrochemiluminescence (ECL) in the evaluation of pediatric patients with spina bifida and NL-sensitized adult health care workers. As with RAST and ELISA, ECL is capable of detecting picogram amounts of specific analyte. The ECL assay detected NL-specific immunoglobulin E (NL-IgE) in three of six health care workers with strong histories of NL hypersensitivity. All six patients were negative by FCA. Further, 2 of 11 spina bifida patients found to be NL-IgE negative by FCA were NL-IgE positive by ECL. These findings suggest that in sensitivity the ECL assay is an improvement over the FCA for the identification of NL-sensitive individuals.
AuthorsL Kobrynski, L Tanimune, N A Pawlowski, S D Douglas, D E Campbell
JournalClinical and diagnostic laboratory immunology (Clin Diagn Lab Immunol) Vol. 3 Issue 1 Pg. 42-6 (Jan 1996) ISSN: 1071-412X [Print] United States
PMID8770502 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antigens
  • Latex
  • Immunoglobulin E
Topics
  • Adult
  • Antigens
  • Case-Control Studies
  • Child
  • Evaluation Studies as Topic
  • Flow Cytometry (methods, statistics & numerical data)
  • Health Personnel
  • Humans
  • Hypersensitivity (diagnosis, immunology)
  • Immunoglobulin E (analysis, blood)
  • Latex (adverse effects, immunology)
  • Luminescent Measurements
  • Microspheres
  • Occupational Diseases (immunology)
  • Sensitivity and Specificity
  • Spinal Dysraphism (immunology)

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