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Emerging Aspergillus Species Almost Exclusively Associated With Primary Immunodeficiencies

  1. Author:
    Seyedmousavi, S.
    Lionakis, M. S.
    Parta,Mark
    Peterson, S. W.
    Kwon-Chung, K. J.
  2. Author Address

    NIAID, Mol Microbiol Sect, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USA.NIAID, Fungal Pathogenesis Sect, Lab Clin Immunol & Microbiol, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USA.NCI, Clin Res Directorate, Clin Monitoring Res Program, Frederick Natl Lab Canc Res, Frederick, MD 21701 USA.USDA, Natl Ctr Agr Utilizat Res, Peoria, IL USA.
    1. Year: 2018
    2. Date: Sep
    3. Epub Date: 2018 09 26
  1. Journal: Open forum infectious diseases
  2. OXFORD UNIV PRESS INC,
    1. 5
    2. 9
  3. Type of Article: Review
  4. Article Number: ofy213
  5. ISSN: 2328-8957
  1. Abstract:

    Invasive aspergillosis (IA) is the most serious mold infection encountered in patients with iatrogenic immunosuppression. IA is also a major cause of mortality and morbidity in individuals with primary immunodeficiency (PID). Although Aspergillus fumigatus is the most common etiologic agent of IA reported in PID patients, followed by A. nidulans, multiple poorly recognized Aspergillus species such as A. udagawae, A. quadrilineatus, A. pseudoviridinutans, A. tanneri, A. subramanianii, and A. fumisynnematus have been reported almost exclusively from patients with inborn defects in host antifungal defense pathways. Infection in PID patients exhibits patterns of disease progression distinct from those in iatrogenic immunosuppression. Specifically, the disease can be extrapulmonary and chronic with a tendency to disseminate in a contiguous manner across anatomical planes. It is also more refractory to standard antifungal therapy. This synopsis summarizes our understanding of emerging rare Aspergillus species that primarily affect patients with PIDs but not those with acquired immunodeficiencies.

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External Sources

  1. DOI: 10.1093/ofid/ofy213
  2. PMID: 30568990
  3. PMCID: PMC6157306
  4. WOS: 000446084900016

Library Notes

  1. Fiscal Year: FY2018-2019
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