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三位 SAVI 综合征患者在使用 Janus 激酶抑制剂的情况下进行肺移植。

Lung Transplantation under a Janus Kinase Inhibitor in Three Patients with SAVI Syndrome.

机构信息

Service de Pneumologie Pédiatrique, Hôpital Femme-Mère-Enfant, Hospices Civils de Lyon, Lyon, France.

Service de Rhumatologie, Néphrologie Et Dermatologie Pédiatrique, CMR RAISE, Hôpital Femme-Mère-Enfant, Hospices Civils de Lyon, Lyon, France.

出版信息

J Clin Immunol. 2023 Nov;43(8):2156-2164. doi: 10.1007/s10875-023-01595-4. Epub 2023 Oct 10.

Abstract

Stimulator of interferon genes (STING)-associated vasculopathy with onset in infancy (SAVI) is a very rare autoinflammatory disease related to STING1 mutation. SAVI is mainly characterized by fever attacks and skin and respiratory manifestations such as interstitial lung disease or alveolar hemorrhage. Respiratory involvement occurs in 80% of cases and might progress to severe lung fibrosis and require lung transplantation (LT). Three patients with SAVI who underwent LT have been reported to date. Two of the three patients died months or years after LT due to multiple organ failure or sepsis. However, the diagnosis of SAVI was made after LT, thus preventing the use of targeted therapy, such as the Janus kinase 1 and 2 inhibitor (JAK1/2i) ruxolitinib, which might be beneficial for the respiratory status of these patients. We aimed to report our experience in managing three patients who were followed in three large lung transplantation centers in France and who benefited from ruxolitinib before undergoing LT. We describe posttransplant complications that occurred as well as outcomes.

摘要

干扰素基因刺激物 (STING)-相关婴儿起病的血管病 (SAVI) 是一种与 STING1 突变相关的非常罕见的自身炎症性疾病。SAVI 的主要特征是发热发作以及皮肤和呼吸道表现,如间质性肺病或肺泡出血。80%的病例存在呼吸道受累,并可能进展为严重的肺纤维化,需要进行肺移植 (LT)。迄今为止,已有 3 例 SAVI 患者接受了 LT。这 3 例患者中的 2 例在 LT 后数月或数年内因多器官衰竭或败血症而死亡。然而,SAVI 的诊断是在 LT 之后做出的,从而阻止了使用靶向治疗,如 Janus 激酶 1 和 2 抑制剂 (JAK1/2i) 芦可替尼,这可能对这些患者的呼吸状况有益。我们旨在报告我们在法国三个大型肺移植中心随访的 3 例患者的经验,这些患者在接受 LT 之前受益于芦可替尼。我们描述了移植后出现的并发症和结局。

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