Chinese Patients with Defective IL-12/23-Interferon-γ Circuit in Taiwan: Partial Dominant Interferon-γ Receptor 1 Mutation Presenting as Cutaneous Granuloma and IL-12 Receptor β1 Mutation as Pneumatocele (original) (raw)
Abstract
Background
IL-12/23-interferon-γ circuit enhances reactive oxygen species (ROS) synthesis in macrophage to attack intracellular pathogens such as mycobacteria and salmonella. Defective ROS in patients with chronic granulomatous disease (CGD) have increased susceptibility to these pathogens. However, patients with defective IL-12/23-interferon-γ circuit rather than CGD are not recognized in Taiwan, endemic for tuberculosis and salmonella.
Aim
The purpose of this study was to identify Taiwanese patients with defective IL-12/23-IFN-γ circuit.
Patients and Methods
In a long-term molecular study of primary immunodeficiency diseases (PIDD), the tentative CGD patients presenting with Bacille Calmette–Guerin (BCG)-induced infection, refractory atypical mycobacterial cutaneous granuloma and osteomyelitis, recurrent salmonella sepsis, and pneumatocele were studied for the IL-12/23-IFN-γ circuit. ROS was first measured to exclude CGD. Candidate genes of IL12RB1, IFNRG1, IL12p40, IFNRG2, signal transducer and activator of transcription-1, and NF-κB essential modulator and their encoding protein expressions were analyzed.
Results
Of the 175 Taiwanese PIDD patients during a 28-year period, three patients from two unrelated families were identified with the hotspot INFRG1 deletion mutation (818del4) and had CGD features, presenting as cutaneous granuloma, and multiple osteomyelitis infected by non-tuberculosis mycobacteria, Mycobacteria avium complex and Mycobacterium scrofulaceum. Another with mis-sense IL12RB1 mutation (Arg211Pro) was noted as recurrent Salmonella enteritidis D sepsis and pneumatocele.
Conclusion
Patients with defective IL-12/23-IFN-γ circuit may resemble or overlap CGD manifestations of refractory cutaneous atypical mycobacterial granuloma and salmonella pneumatocele.
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Abbreviations
BCG:
Bacille Calmette–Guerin
CMC:
chronic mucocutaneous candidiasis
PBMCs:
peripheral blood mononuclear cells
PIDD:
primary immunodeficiency diseases
ROS:
reactive oxygen species
SCID:
severe combined immunodeficiency
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Acknowledgments
The authors wish to thank all of the patients and their families for their kind cooperation, as well as their physicians for the referrals. They also thank Yi-Chen Wang, Hsiu-Li Chou, and Hsiu-Shan Hsiao for their technical assistance. This study was supported by Chang-Gung Medical Research Progress Grant CMRPG 450061 and National Science Council Grants NSC96-2314-B-182A-053-MY2 and NMRPG466062.
Conflict of interest statement
All of the authors declare no conflict of interest.
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Authors and Affiliations
- Primary Immunodeficiency Care And Research (PICAR) Institute, Chang Gung Memory and Children’s Hospital, Chang Gung University College of Medicine, Taoyuan, Taiwan
Wen-I Lee, Jing-Long Huang & Tang-Her Jaing - Department of Pediatric Allergy, Immunology and Rheumatology, Chang Gung Memory and Children’s Hospital, Chang Gung University College of Medicine, Pediatric Office 12 L, #5 Fu-Shing Street, Kwei-Shan, Taoyuan, Taiwan
Wen-I Lee & Jing-Long Huang - Department of Pediatric Infection, Chang Gung Memory and Children’s Hospital, Chang Gung University College of Medicine, Taoyuan, Taiwan
Tzou-Yien Lin & Cheng-Hsun Chiu - Department of Pathology, Chang Gung Memory and Children’s Hospital, Chang Gung University College of Medicine, Taoyuan, Taiwan
Chuen Hsueh - Department of Medical Imaging and Intervention, Chang Gung Memory and Children’s Hospital, Chang Gung University College of Medicine, Taoyuan, Taiwan
Alex M. Wong - Department of Pediatric Neurology, Chang Gung Memory and Children’s Hospital, Chang Gung University College of Medicine, Taoyuan, Taiwan
Meng-Ying Hsieh - Graduate Institute of Medical Clinics, Chang Gung Memory and Children’s Hospital, Chang Gung University College of Medicine, Taoyuan, Taiwan
Meng-Ying Hsieh - Department of Pediatric Hematology and Oncology, Chang Gung Memory and Children’s Hospital, Chang Gung University College of Medicine, Taoyuan, Taiwan
Tang-Her Jaing
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Lee, WI., Huang, JL., Lin, TY. et al. Chinese Patients with Defective IL-12/23-Interferon-γ Circuit in Taiwan: Partial Dominant Interferon-γ Receptor 1 Mutation Presenting as Cutaneous Granuloma and IL-12 Receptor β1 Mutation as Pneumatocele.J Clin Immunol 29, 238–245 (2009). https://doi.org/10.1007/s10875-008-9253-9
- Received: 12 July 2008
- Accepted: 09 September 2008
- Published: 01 October 2008
- Issue Date: March 2009
- DOI: https://doi.org/10.1007/s10875-008-9253-9