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成人巨噬细胞活化综合征-噬血细胞性淋巴组织细胞增生症:“关于血浆置换和免疫抑制升级策略”——单中心反思。

Adult macrophage activation syndrome-haemophagocytic lymphohistiocytosis: 'of plasma exchange and immunosuppressive escalation strategies' - a single centre reflection.

机构信息

Department of Nephrology, Klinikum rechts der Isar, Technical University Munich, Munich, Germany.

II Medizinische Klinik, Klinikum rechts der Isar, Technical University Munich, Munich, Germany.

出版信息

Lupus. 2020 Mar;29(3):324-333. doi: 10.1177/0961203320901594. Epub 2020 Feb 3.

Abstract

OBJECTIVE

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).

METHODS

Here we report a retrospective series of steroid refractory MAS-HLH, the associated therapeutic regimes and outcomes.

RESULTS

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.

CONCLUSION

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.

摘要

目的

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。

方法

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。

结果

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。

结论

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。

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