Schiepek Tim, Grün Pascal, Turhani Flora, Grün Ann-Sophie, Holzhauer Sophie, Turhani Dritan
Center for Oral and Maxillofacial Surgery, Department of Dentistry, Faculty of Medicine and Dentistry, Danube Private University, Steiner Landstraße 124, 3500 Krems, Austria.
Center for Oral and Maxillofacial Surgery, Department of Dentistry, Faculty of Medicine and Dentistry, Danube Private University, Steiner Landstraße 124, 3500 Krems, Austria; Clinical Application of Artificial Intelligence in Dentistry (CAAID) Group, Department of Dentistry, Faculty of Medicine and Dentistry, Danube Private University, Steiner Landstraße 124, 3500 Krems an der Donau, Austria.
Int J Surg Case Rep. 2025 Jun 30;133:111593. doi: 10.1016/j.ijscr.2025.111593.
Secondary Sjögren's syndrome (sSD) is a typical oral manifestation of systemic lupus erythematosus (SLE), which manifests itself in the form of xerostomia and mucositis and often makes dental treatment more complex. Anifrolumab, a type I interferon receptor antagonist (IFNAR1), was recently approved for the treatment of moderate-to-severe SLE. However, its potential benefit in sSD-particularly in addressing oral disease burden-remains unreported.
We describe a 40-year-old woman diagnosed with SLE, secondary Sjögren's syndrome, rheumatoid arthritis, and osteopenia, who presented with persistent xerostomia, mucosal inflammation, joint pain, and cutaneous lupus despite long-term immunosuppressive therapy. Anifrolumab (300 mg IV every 28 days) was initiated in November 2022. Over the subsequent six months, the patient experienced marked improvement in cutaneous and systemic symptoms, alongside enhanced salivary flow and reduced oral inflammation. The resolution of xerostomia facilitated successful dental rehabilitation, including sinus floor augmentation, socket preservation and dental implant-supported prosthetics.
This case illustrates the broader therapeutic potential of interferon blockade in autoimmune diseases with mucosal involvement. By targeting IFNAR1, anifrolumab may interrupt the pathogenic loop of type I interferon-driven inflammation and B-cell dysregulation, resulting in both systemic and oral clinical improvement.
Anifrolumab may offer meaningful benefit for patients with secondary Sjögren's syndrome beyond conventional SLE control, particularly in improving oral health outcomes. Further clinical studies are warranted to evaluate its efficacy in mucosal autoimmune manifestations.
继发性干燥综合征(sSD)是系统性红斑狼疮(SLE)的典型口腔表现,以口干症和口腔炎的形式出现,常使牙科治疗更为复杂。阿尼鲁单抗是一种I型干扰素受体拮抗剂(IFNAR1),最近被批准用于治疗中重度SLE。然而,其在sSD中的潜在益处,特别是在减轻口腔疾病负担方面,尚未见报道。
我们描述了一名40岁女性,诊断为SLE、继发性干燥综合征、类风湿关节炎和骨质减少,尽管长期接受免疫抑制治疗,但仍有持续性口干、黏膜炎症、关节疼痛和皮肤狼疮。2022年11月开始使用阿尼鲁单抗(每28天静脉注射300mg)。在随后的六个月里,患者的皮肤和全身症状明显改善,唾液分泌增加,口腔炎症减轻。口干症的缓解促进了成功的牙齿修复,包括上颌窦底提升、牙槽窝保存和牙种植体支持的修复体。
本病例说明了干扰素阻断在伴有黏膜受累的自身免疫性疾病中的更广泛治疗潜力。通过靶向IFNAR1,阿尼鲁单抗可能会中断I型干扰素驱动的炎症和B细胞失调的致病循环,从而导致全身和口腔临床症状改善。
阿尼鲁单抗可能为继发性干燥综合征患者带来超越传统SLE控制的显著益处,特别是在改善口腔健康结局方面。有必要进行进一步的临床研究以评估其在黏膜自身免疫表现中的疗效。