Chen Ni, Liang Hanlin, Liang Siqiao, Liang Xiaona, Huang Xuemei, Yu Qingliang, He Zhiyi
Department of Respiratory and Critical Care Medicine, The First Affiliated Hospital of Guangxi Medical University, No.6 Shuang Yong Road, Nanning, 530021, Guangxi, China.
Department of International Medical Services, The Affiliated Tumor Hospital of Guangxi Medical University, Nanning, Guangxi, China.
BMC Immunol. 2025 Mar 8;26(1):17. doi: 10.1186/s12865-025-00696-6.
Anti-interferon-γ autoantibodies (AIGAs) syndrome is a recently recognized adult-onset immunodeficiency syndrome. Serum Immunoglobulin E (IgE) is increased in AIGAs syndrome, but the role of serum IgE levels in the clinical features and disease outcomes of AIGAs syndrome is not clear.
We retrospectively enrolled 163 patients diagnosed AIGAs syndrome with serum IgE examined at baseline from 2021 to 2024 and compared the clinical features between Group A (serum IgE level ≤ 212 IU/mL) and Group B (serum IgE level > 212 IU/mL). Multivariable logistic regression method was used to explore the risk factors associated with disease outcomes.
163 patients were included in this study, of whom 97 patients were in Group A (serum IgE level ≤ 212 IU/mL) and 66 patients in Group B (serum IgE level > 212 IU/mL). Group B showed higher number of infectious episodes, elevated levels of erythrocyte sedimentation rate (ESR), CD3 + T cells, immunoglobulin G (IgG), IgA, and globulins (GLB), shorter progression-free survival (PFS), and increased exacerbation numbers. Group B exhibited a higher incidence of fatigue, dyspnea, loss of appetite, rash, moist rales, hepatomegaly, and splenomegaly. Skin, bone marrow and spleen involvements were more common in Group B. IgE demonstrated correlations with IgG, GLB, Albumin (ALB), Eosinophils (EOS), IgG4, and ESR. During the follow-up, Group B exhibiting higher number of exacerbations compared to Group A (P < 0.0001). Multivariable Cox regression analysis revealed that High AIGAs titers (hazard ratio [HR], 2.418, 95% confidence interval [CI]1.037-5.642, P = 0.041), WBC > 22.52 × 10cells/L (HR2.199, 95%CI1.194-4.050, P = 0.012) were independent risk factors of disease exacerbation. Glucocorticoid treatment was commonly used in patients with AIGAs syndrome who had elevated IgE levels and skin involvement, demonstrating efficacy in improving condition.
Elevated serum IgE levels are associated with more severe clinical features in AIGAs syndrome, including increased infectious episodes, elevated inflammatory markers/immune markers, and multi-organ involvement, particularly skin. IgE serves as a marker of skin involvement and may indicate a potential response to glucocorticoid treatment.
抗干扰素-γ自身抗体(AIGAs)综合征是一种最近才被认识的成人发病的免疫缺陷综合征。AIGAs综合征患者血清免疫球蛋白E(IgE)升高,但血清IgE水平在AIGAs综合征临床特征及疾病转归中的作用尚不清楚。
我们回顾性纳入了2021年至2024年诊断为AIGAs综合征且基线时检测了血清IgE的163例患者,并比较了A组(血清IgE水平≤212 IU/mL)和B组(血清IgE水平>212 IU/mL)的临床特征。采用多变量逻辑回归方法探讨与疾病转归相关的危险因素。
本研究共纳入163例患者,其中A组97例(血清IgE水平≤212 IU/mL),B组66例(血清IgE水平>212 IU/mL)。B组感染发作次数更多,红细胞沉降率(ESR)、CD3 + T细胞、免疫球蛋白G(IgG)、IgA和球蛋白(GLB)水平升高,无进展生存期(PFS)更短,病情加重次数增加。B组疲劳、呼吸困难、食欲不振、皮疹、湿啰音、肝肿大和脾肿大的发生率更高。皮肤、骨髓和脾脏受累在B组中更常见。IgE与IgG、GLB、白蛋白(ALB)、嗜酸性粒细胞(EOS)、IgG4和ESR相关。随访期间,B组病情加重次数高于A组(P<0.0001)。多变量Cox回归分析显示,高AIGAs滴度(风险比[HR],2.418,95%置信区间[CI]1.037 - 5.642,P = 0.041)、白细胞>22.52×10⁹/L(HR 2.199,95%CI 1.194 - 4.050,P = 0.012)是疾病加重的独立危险因素。糖皮质激素治疗常用于IgE水平升高且有皮肤受累的AIGAs综合征患者,显示出改善病情的疗效。
血清IgE水平升高与AIGAs综合征更严重的临床特征相关,包括感染发作增加、炎症标志物/免疫标志物升高以及多器官受累,尤其是皮肤。IgE是皮肤受累的标志物,可能提示对糖皮质激素治疗的潜在反应。