Department of Nephrology, Klinikum rechts der Isar, Technical University Munich, Munich, Germany.
II Medizinische Klinik, Klinikum rechts der Isar, Technical University Munich, Munich, Germany.
Lupus. 2020 Mar;29(3):324-333. doi: 10.1177/0961203320901594. Epub 2020 Feb 3.
In the context of systemic autoimmunity, that is systemic lupus erythematosus (SLE) or adult-onset Still's disease (AOSD), secondary haemophagocytic lymphohistiocytosis (HLH; also referred to as macrophage activation syndrome (MAS) or more recently MAS-HLH) is a rare and potentially life-threatening complication. Pathophysiological hallmarks are aberrant macrophage and T cell hyperactivation and a systemic cytokine flare, which generate a sepsis-like, tissue-damaging, cytopenic phenotype. Unfortunately, for adult MAS-HLH we lack standardized treatment protocols that go beyond high-dose corticosteroids. Consequently, outcome data are scarce on steroid refractory cases. Aside from protocols based on treatment with calcineurin inhibitors, etoposide, cyclophosphamide and anti-IL-1, favourable outcomes have been reported with the use of intravenous immunoglobulin (IvIG) and plasma exchange (PE).
Here we report a retrospective series of steroid refractory MAS-HLH, the associated therapeutic regimes and outcomes.
In this single-centre experience, 6/8 steroid refractory patients survived (median follow-up: 54.4 (interquartile range: 23.3-113.3) weeks). All were initially treated with PE, which induced partial response in 5/8 patients. Yet, all patients required escalation of immunosuppressive therapies. One case of MAS-HLH in new-onset AOSD had to be escalated to etoposide, whereas most SLE-associated MAS-HLH patients responded well to cyclophosphamide. Relapses occurred in 2/8 cases.
Together, early use of PE is at most a supportive measure, not a promising monotherapy of adult MAS-HLH. In refractory cases, conventional cytoreductive therapies (i.e. cyclophosphamide and etoposide) constitute potent and reliable rescue approaches, whereas IvIG, anti-thymoglobulin, and biologic agents appear to be less effective.
在系统性自身免疫性疾病(如系统性红斑狼疮[SLE]或成人Still 病[AOSD])的背景下,继发性噬血细胞性淋巴组织细胞增生症(HLH;也称为巨噬细胞活化综合征[MAS]或最近的 MAS-HLH)是一种罕见且潜在危及生命的并发症。其病理生理学特征为异常的巨噬细胞和 T 细胞过度激活以及全身性细胞因子爆发,导致类似脓毒症、组织损伤、血细胞减少的表型。不幸的是,对于成人 MAS-HLH,我们缺乏超出大剂量皮质类固醇的标准化治疗方案。因此,对于类固醇难治性病例,结果数据稀缺。除了基于钙调神经磷酸酶抑制剂、依托泊苷、环磷酰胺和抗白细胞介素-1 治疗的方案外,静脉注射免疫球蛋白(IVIG)和血浆置换(PE)的应用也取得了有利的结果。
我们在此报告一系列类固醇难治性 MAS-HLH 的回顾性系列研究,包括相关治疗方案和结局。
在本单中心经验中,8 例类固醇难治性 MAS-HLH 患者中有 6 例存活(中位随访时间:54.4(四分位距:23.3-113.3)周)。所有患者最初均接受 PE 治疗,8 例中有 5 例患者的病情得到部分缓解。然而,所有患者均需要升级免疫抑制治疗。1 例新发 AOSD 相关性 MAS-HLH 病例需要升级为依托泊苷,而大多数 SLE 相关性 MAS-HLH 患者对环磷酰胺反应良好。8 例中有 2 例出现复发。
PE 的早期应用最多只是一种支持性措施,而不是治疗成人 MAS-HLH 的有前途的单一疗法。在难治性病例中,传统的细胞减灭治疗(即环磷酰胺和依托泊苷)是有效的、可靠的挽救方法,而 IVIG、抗胸腺球蛋白和生物制剂的疗效似乎较差。