Jordan Victoria, Pickles Robert
1Department of Infectious Diseases, John Hunter Hospital, New Lambton Heights, NSW 2305, Australia.
2School of Medicine and Public Health, University of Newcastle, Callaghan, NSW 2308, Australia.
Eur J Microbiol Immunol (Bp). 2025 Jan 10;15(1):57-61. doi: 10.1556/1886.2024.00123. Print 2025 Mar 19.
Interferon-gamma (IFN-γ) autoantibody syndrome is an emerging clinical entity that has been associated with disseminated non-tuberculous mycobacterial infection (dNTM) particularly in healthy young people, a population not previously thought to be at particular risk. A 29-year-old South-East Asian man presented with several weeks of fever, cough, lymphadenopathy, and constitutional symptoms while working on an international cargo ship, deteriorating rapidly with a sepsis-like syndrome. Eventually lymph node and sputum cultures revealed a diagnosis of dNTM infection with growth of both Mycobacterium persicum and Mycobacterium abscessus. He was commenced on rituximab as well as combination anti-mycobacterial therapy with good clinical response. This case highlights some of the difficulties faced by patients with dNTM in the context of IFN-γ autoantibodies, particularly delayed diagnosis, and lack of evidence base surrounding optimal management. Further research into long-term outcomes and treatment is required as well as increased awareness among clinicians.
干扰素-γ(IFN-γ)自身抗体综合征是一种新出现的临床病症,与播散性非结核分枝杆菌感染(dNTM)相关,特别是在健康年轻人中,而这一人群以前未被认为有特别风险。一名29岁的东南亚男子在一艘国际货船上工作时,出现了数周的发热、咳嗽、淋巴结病和全身症状,并迅速恶化为类似脓毒症的综合征。最终,淋巴结和痰液培养显示诊断为dNTM感染,培养出了波斯分枝杆菌和脓肿分枝杆菌。他开始接受利妥昔单抗以及联合抗分枝杆菌治疗,临床反应良好。该病例凸显了dNTM患者在IFN-γ自身抗体背景下所面临的一些困难,尤其是诊断延迟以及缺乏关于最佳治疗的循证依据。需要对长期预后和治疗进行进一步研究,并提高临床医生的认识。