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Interpretation of Dihydrorhodamine-1,2,3 Flow Cytometry in Chronic Granulomatous Disease: an Atypical Exemplar

  1. Author:
    Donko, Agnes
    Kuhns,Doug
    Cousin, Margot A
    Smith, Matthew J
    Sacco, Keith A
    Klee, Eric W
    Joshi, Avni Y
    Gavrilova, Ralitza H
    Holland, Steven M
    Leto, Thomas L
    Abraham, Roshini S
  2. Author Address

    Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA., Leidos Biomedical Research, Inc, Frederick National Laboratory for Cancer Research, Frederick, MD, USA., Center for Individualized Medicine, Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, USA., Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA., Department of Internal Medicine, Mayo Clinic, Jacksonville, FL, USA., Department of Clinical Genomics, Mayo Clinic, Rochester, MN, USA., Division of Allergy and Immunology, Department of Medicine and Department of Pediatrics, Mayo Clinic, Rochester, MN, USA., Department of Neurology, Mayo Clinic, Rochester, MN, USA., Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA. tleto@nih.gov., Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA. Roshini.Abraham@nationwidechildrens.org., Department of Pathology and Laboratory Medicine, Nationwide Children 39;s Hospital, Columbus, OH, USA. Roshini.Abraham@nationwidechildrens.org.,
    1. Year: 2022
    2. Date: Mar 28
    3. Epub Date: 2022 03 28
  1. Journal: Journal of Clinical Immunology
  2. Springer
  3. Type of Article: Article
  1. Abstract:

    This is a functional characterization of a novel CYBA variant associated with normal DHR flow cytometry. Chronic granulomatous disease (CGD) is an inborn error of immunity characterized by recurrent bacterial and fungal infections and dysregulated inflammatory responses due to defective phagocytic cell function leading to the formation of granulomas. CGD patients have pathogenic variants in any of the five components of the phagocytic NADPH oxidase, which transfers electrons through the phagosomal membrane and produces superoxide upon bacterial uptake. Here, we report a pediatric female patient with a novel homozygous missense variant (c.293C?>?T, p.(Ser98Leu)) in CYBA, encoding the p22phox protein, associated with autosomal recessive CGD. The patient presented with severe recurrent pneumonia. Specific pathogens identified included Burkholderia and Serratia species suggesting neutrophil functional abnormalities; however, the dihydrorhodamine-1,2,3 (DHR) flow cytometric and cytochrome c reduction assays for neutrophil respiratory burst fell within the low side of the normal range. Western blot and flow cytometric analysis of individual NADPH oxidase components revealed reduced levels of p22phox and gp91phoxphox proteins. The pathological consequence of the p.Ser98Leu variant was further evaluated in heterologous expression systems, which confirmed reduced p22phox protein stability and oxidase activity. Although this patient did not exhibit all the classic features of CGD, such as granulomas and skin infections, she had recurrent pneumonias with oxidant-sensitive pathognomonic organisms, resulting in appropriate targeted CGD testing. This case emphasizes the need to contextually interpret laboratory data, especially using clinical findings to direct additional assessments including genetic analysis. © 2022. This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply.

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External Sources

  1. DOI: 10.1007/s10875-022-01217-5
  2. PMID: 35344128
  3. PII : 10.1007/s10875-022-01217-5

Library Notes

  1. Fiscal Year: FY2021-2022
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