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Clinical manifestations, course, and outcome of patients with neutralizing anti-interferon-γ autoantibodies and disseminated nontuberculous mycobacterial infections

  • Chih Yu Chi
  • , Chia Hao Lin
  • , Mao Wang Ho
  • , Jing Ya Ding
  • , Wen Chi Huang
  • , Han-Po Shih
  • , Chun Fu Yeh
  • , Chang Phone Fung
  • , Hsin Yun Sun
  • , Ching Tai Huang
  • , Ting Shu Wu
  • , Chih Yen Chang
  • , Yuag Meng Liu
  • , Jia Yih Feng
  • , Wei Kai Wu
  • , Lih Shinn Wang
  • , Chung Hao Tsai
  • , Cheng Mao Ho
  • , Huang-Shen Lin
  • , Hung Jen Chen
  • Po Chang Lin, Wei Chin Liao, Wei Ting Chen, Chia Chi Lo, Shang Yu Wang, Chen Yen Kuo, Chen Hsiang Lee, Cheng Lung Ku*
*Corresponding author for this work
  • Chang Gung University
  • China Medical University Taichung
  • Chang Gung Memorial Hospital
  • Veterans General Hospital-Taipei
  • National Taiwan University
  • Changhua Christian Hospital
  • Buddhist Tzu-Chi General Hospital Taiwan
  • Koo Foundation Sun Yat-Sen Cancer Center

Research output: Contribution to journalJournal Article peer-review

128 Scopus citations

Abstract

Neutralizing anti-interferon-γ autoantibody (nAIGA)-associated immunodeficiency is an emerging medical issue worldwide. In the present study, we describe and discuss the clinical features and outcomes of patients with nAIGAs and disseminated infections by nontuberculous mycobacteria (dNTM). We thoroughly reviewed the medical records of all patients. Microorganisms and nAIGAs were identified using previously described methods with modifications. All data were calculated and analyzed using SPSS software. Among 46 adult patients with dNTM infections, we identified 45 cases (97.8%) with nAIGAs. The average patient age was 58.6 years, and there was no sex predominance. Cervical lymphadenitis (81.8%) was the most common clinical manifestation. Endocrine disorder was the leading comorbidity (7 cases). Malignancies were found in 4 patients, and all of the malignancies originated from the T-cell/macrophage lineage. More than half of the identifiable isolates were slow-growing NTMs. Twenty-eight (62.2%) and 18 (40.0%) patients had a history of zoster and salmonellosis, respectively. A high proportion of patients with recurrent episodes of NTM infection or a history of zoster and dNTM infection had initial nAIGA titers ≥10 -5 dilution (P<0.05). Twenty-seven patients (60.0%) required long-term antimycobacterial therapy and had at least 1 episode of recurrent NTM disease. No mortality was related to dNTM infection. In Taiwan, nAIGAs are a recently recognized mechanism of dNTM infection. Long term of antibiotic treatment and adherence to medical advice are necessary to improve the clinical outcome of patients with nAIGAs.

Original languageEnglish
Article numbere3927
JournalMedicine (United States)
Volume95
Issue number25
DOIs
StatePublished - 01 06 2016

Bibliographical note

Publisher Copyright:
© 2016 Wolters Kluwer Health, Inc.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Taiwan
  • autoantibody
  • interferon-gamma
  • nontuberculous mycobacterium

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