Chronic granulomatous disease (CGD) and complete myeloperoxidase deficiency both yield strongly reduced dihydrorhodamine 123 test signals but can be easily discerned in routine testing for CGD

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • L. Mauch - (Author)
  • A. Lun - , Charité – Universitätsmedizin Berlin (Author)
  • M.R. O'Gorman - , Ann and Robert H. Lurie Children's Hospital of Chicago (Author)
  • J.S. Harris - (Author)
  • I. Schulze - , Charité – Universitätsmedizin Berlin (Author)
  • A. Zychlinsky - , Max Planck Institute for Infection Biology (Author)
  • T. Fuchs - , Max Planck Institute for Infection Biology (Author)
  • U. Oelschlägel - , Department of internal Medicine I (Author)
  • S. Brenner - , Department of Paediatrics (Author)
  • D. Kutter - , Laboratoires Réunis (Author)
  • A. Rösen-Wolff - , Department of Paediatrics (Author)
  • J. Roesler - (Author)

Abstract

Background: The flow cytometric dihydrorhodamine 123 (DHR) assay is used as a screening test for chronic granulomatous disease (CGD), but complete myeloperoxidase (MPO) deficiency can also lead to a strongly decreased DHR signal. Our aim was to devise simple laboratory methods to differentiate MPO deficiency (false positive for CGD) and NADPH oxidase abnormalities (true CGD).

Methods: We measured NADPH-oxidase and MPO activity in neutrophils from MPO-deficient patients, CGD patients, NADPH-oxidase-transfected K562 cells and cells with inhibited and substituted MPO.

Results: Eosinophils from MPO-deficient individuals retain eosinophilic peroxidase and therefore generate a normal DHR signal. The addition of recombinant human MPO enhances the DHR signal when simply added to a suspension of MPO-deficient cells but not when added to NADPH-oxidase-deficient (CGD) cells. Lucigenin-enhanced chemiluminescence (LCL) is increased in neutrophils from MPO-deficient patients, whereas neutrophils from patients with CGD show a decreased response.

Conclusions: A false-positive result caused by MPO deficiency can be easily ascertained because, unlike cells from a CGD patient, cells from MPO-deficient patients (a) contain functionally normal eosinophils, (b) show a significant enhancement of the DHR signal following addition of rhMPO, and (c) generate a strong LCL signal.

Details

Original languageEnglish
Pages (from-to)890-896
Number of pages7
JournalClinical Chemistry
Volume53
Issue number5
Publication statusPublished - 1 May 2007
Peer-reviewedYes

External IDs

Scopus 34248342558
researchoutputwizard legacy.publication#19641
ORCID /0000-0002-3666-7128/work/147143650

Keywords

Sustainable Development Goals