Neutrophil functions in patients with inherited bone marrow failure syndromes

Andrzej Rochowski, Chunxiang Sun, Michael Glogauer, Blanche P. Alter

Research output: Contribution to journalArticlepeer-review

Abstract

Background: The inherited bone marrow failure syndromes (IBMFS) include Fanconi anemia, dyskeratosis congenita, Diamond-Blackfan anemia, and Shwachman-Diamond syndrome (SDS). Previous studies reported decreased neutrophil chemotaxis in patients with SDS; there are no reports of neutrophil function in other IBMFS. In this study we examined neutrophil respiratory burst function in IBMFS patients. Procedure: Samples from 43 IBMFS patients and 61 healthy family members were collected, shipped, and analyzed within 24hr. We also studied samples from 12 healthy control persons immediately after collection. Neutrophils were stimulated with phorbol 12-myristate acetate (PMA) and N-formyl-methyonyl-leucyl-phenylalanine (fMLP), and respiratory burst analyzed by reduction of dihydro-rhodamine and cytochrome c. Results: There was no significant difference in the degree of fMLP or PMA-driven respiratory burst activity between each of the IBMFS subgroups and their respective family members. There was also no difference in respiratory burst activity between any IBMFS, pooled group of all healthy family members and healthy controls. Conclusions: Neutrophil respiratory burst activity from IBMFS patients does not differ from that of healthy family members and controls.

Original languageEnglish (US)
Pages (from-to)306-309
Number of pages4
JournalPediatric Blood and Cancer
Volume57
Issue number2
DOIs
StatePublished - Aug 2011
Externally publishedYes

Keywords

  • Inherited bone marrow failure
  • Neutrophil
  • Respiratory burst

ASJC Scopus subject areas

  • Oncology
  • Pediatrics, Perinatology, and Child Health
  • Hematology

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