Clinical course and outcomes of patients with anti-interferon-gamma autoantibody-associated adult-onset immunodeficiency: an observational cohort study
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Issued Date
2025-12-01
Resource Type
eISSN
13652060
Scopus ID
2-s2.0-105021874938
Pubmed ID
41229127
Journal Title
Annals of Medicine
Volume
57
Issue
1
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SCOPUS
Bibliographic Citation
Annals of Medicine Vol.57 No.1 (2025) , 2565446
Suggested Citation
Angkasekwinai N., Wongsawat E., Vorasan N. Clinical course and outcomes of patients with anti-interferon-gamma autoantibody-associated adult-onset immunodeficiency: an observational cohort study. Annals of Medicine Vol.57 No.1 (2025) , 2565446. doi:10.1080/07853890.2025.2565446 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/113163
Title
Clinical course and outcomes of patients with anti-interferon-gamma autoantibody-associated adult-onset immunodeficiency: an observational cohort study
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Abstract
BACKGROUND: Anti-interferon-gamma autoantibody (anti-IFN-γ-auto-Abs)-associated adult-onset immunodeficiency (AOID) syndrome presents with variable clinical manifestations, and long-term outcome data and natural history remain limited. MATERIALS AND METHODS: This single-center study utilized a disease registry of AOID patients (≥18 years) at Siriraj Hospital, Bangkok, Thailand. Clinical outcomes (survival, death, loss to follow-up) as of November 20, 2024 and disease status (remission, non-remission) at each visit were analyzed. RESULTS: A total of 65 patients were recorded over an eight-year period between 2017 and 2024. The mean age of all patients was 56.4 years, and 66% were female. At initial presentation, 95 opportunistic infections were isolated from 61 patients. M. abscessus (44.2%) was the predominant pathogens, followed by M. avium complex (13.7%), salmonellosis (9.5%) and M. tuberculosis (8.4%). Among 53 patients with at least one year of follow-up, 12 (22.6%) achieved remission and 41 (77.4%) remained in non-remission. Antibody levels exhibited a significant decline over time (p < 0.05) across all patients. However, no significant difference in antibody levels was observed between remission and non-remission group (p > 0.05). Notably, median baseline and latest antibody concentration were significantly lower in the remission group compared to the non-remission group, respectively (baseline level: 3.5, IQR 2.8-3.8 vs. 4.0, IQR 3.5-4.2, p = 0.030; latest level: 2.1, IQR 1.8-2.4 vs. 3.0, IQR 2.1-3.6, p = 0.044). CONCLUSION: This study noted a slight shift in pathogen distribution, even though rapidly growing mycobacteria remain the most common infection. Most patients experienced non-remission, necessitating prolonged antimicrobial therapy. Our findings indicate a declining trend in antibody levels over time. Given the high rates of non-remission and the associated need for extended treatment, immunomodulatory agents should be considered, especially for non-remission patients, to potentially reduce antibody levels and the risk of infection recurrence.