Department of General Medicine, Oita University Faculty of Medicine, 1-1 Idaigaoka, Hasama-Machi, Yufu, Oita, 879-5593, Japan.
BMC Infect Dis. 2023 Jan 30;23(1):58. doi: 10.1186/s12879-023-08020-6.
Disseminated nontuberculous mycobacterial (NTM) infection usually occurs in immunodeficient patients, such as those with human immunodeficiency virus infection and idiopathic CD4 lymphopenia. However, disseminated NTM diseases have also been reported in immunocompetent patients. Autoantibodies to interferon-gamma (IFN-γ) are known to be involved in disseminated NTM disease, although anti-IFN-γ antibodies are mainly seen in immunocompetent patients rather than those with immunodeficiency. Here, we report a rare case of disseminated NTM patient with idiopathic CD4 lymphopenia and anti-IFN-γ antibodies.
A 64-year-old Asian male presented with fever, back pain, anorexia and weight loss. Physical examination revealed subcutaneous masses in the forehead, sternoclavicular joint, and right inguinal region. Computed tomography showed multiple osteosclerotic changes with soft structures and osteolytic changes. Both blood and sputum cultures were positive for Mycobacterium intracellulare, confirming the presence of disseminated NTM infection. Histopathological evaluation of the subcutaneous mass in the right inguinal region showed numerous granulomas consisting of epithelioid cells with Langhans-type giant cells. He was diagnosed with idiopathic CD4 lymphocytopenia. Interestingly, he also had anti-IFN-γ autoantibodies with suppression of IFN-γ-dependent signal transducer and activator of transcription 1 (STAT1) phosphorylation. Two-drug combination therapy with clarithromycin and ethambutol was started for the NTM infection, which resulted in a favorable disease course.
In patients with disseminated NTM infection, idiopathic CD4 lymphocytopenia and anti-IFN-γ autoantibody-positive immunodeficiency can be coexisted. It is necessary to clarify the pathogenesis and clinical course of CD4 lymphocytopenic conditions and IFN-γ neutralizing antibody-positive in the disseminated NTM disease.
播散性非结核分枝杆菌(NTM)感染通常发生于免疫缺陷患者,如人类免疫缺陷病毒感染和特发性 CD4 淋巴细胞减少症患者。然而,免疫功能正常的患者也有播散性 NTM 疾病的报道。干扰素-γ(IFN-γ)的自身抗体被认为与播散性 NTM 疾病有关,尽管抗 IFN-γ 抗体主要见于免疫功能正常的患者,而不是免疫缺陷患者。在此,我们报告一例罕见的特发性 CD4 淋巴细胞减少症伴抗 IFN-γ 抗体的播散性 NTM 患者。
一名 64 岁亚裔男性,因发热、背痛、厌食和体重减轻就诊。体格检查发现额部、胸锁关节和右腹股沟区皮下肿块。计算机断层扫描显示多个骨硬化性改变伴软组织和溶骨性改变。血和痰培养均为细胞内分枝杆菌阳性,证实存在播散性 NTM 感染。右腹股沟区皮下肿块的组织病理学评估显示,大量由上皮样细胞和朗汉斯巨细胞组成的肉芽肿。他被诊断为特发性 CD4 淋巴细胞减少症。有趣的是,他还存在抗 IFN-γ 自身抗体,导致 IFN-γ 依赖性信号转导和转录激活因子 1(STAT1)磷酸化抑制。开始用克拉霉素和乙胺丁醇进行两药联合治疗 NTM 感染,结果疾病过程良好。
在播散性 NTM 感染患者中,特发性 CD4 淋巴细胞减少症和抗 IFN-γ 自身抗体阳性免疫缺陷可同时存在。有必要阐明 CD4 淋巴细胞减少症和 IFN-γ 中和抗体阳性在播散性 NTM 疾病中的发病机制和临床过程。