Holzer Marie-Therese, Nies Jasper F, Oqueka Tim, Huber Tobias B, Kötter Ina, Krusche Martin
III Department of Medicine for Nephrology, Rheumatology and Endocrinology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
II Department of Medicine for Oncology and Pulmonology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Chest. 2023 Jan;163(1):e1-e5. doi: 10.1016/j.chest.2022.08.2209.
Melanoma differentiation-associated gene 5 (MDA5) positive dermatomyositis is a rare systemic autoimmune disease that is associated with life-threatening rapidly progressive interstitial lung disease. We report the case of a 19-year-old male patient with a life-threatening disease course caused by rapidly progressive interstitial lung disease that caused respiratory failure despite intensive immunosuppression with multiple agents (steroids, IV immunoglobulins, tofacitinib, cyclophosphamide, mycophenolate mofetil, ciclosporin and rituximab). Rescue therapy with daratumumab, an anti-CD38-antibody, was initiated. Significant pulmonary improvement was noticed after 4 weekly injections of 1,800 mg. After 6 months of follow up, stable disease remission with significant pulmonary improvement and persistent depletion of CD38+ plasma cells and MDA5-antibody titers were seen. This is the first report of the successful use of daratumumab in dermatomyositis. It highlights the potential of CD38 targeted therapies for severe antibody-mediated autoimmune diseases such as dermatomyositis.
黑色素瘤分化相关基因5(MDA5)阳性皮肌炎是一种罕见的系统性自身免疫性疾病,与危及生命的快速进展性间质性肺病相关。我们报告了一例19岁男性患者,其患有由快速进展性间质性肺病导致的危及生命的病程,尽管使用多种药物(类固醇、静脉注射免疫球蛋白、托法替布、环磷酰胺、霉酚酸酯、环孢素和利妥昔单抗)进行了强化免疫抑制治疗,但仍导致呼吸衰竭。开始使用抗CD38抗体达雷妥尤单抗进行挽救治疗。在每周注射1800mg,共4周后,观察到肺部有显著改善。经过6个月的随访,疾病稳定缓解,肺部有显著改善,CD38+浆细胞持续耗竭,MDA5抗体滴度持续下降。这是关于达雷妥尤单抗成功用于皮肌炎的首例报告。它突出了CD38靶向治疗对于严重抗体介导的自身免疫性疾病如皮肌炎的潜力。