Department of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria.
Section for Medical Statistics (IMS), Center of Medical Statistics, Informatics and Intelligent Systems, Medical University of Vienna, Vienna, Austria.
J Allergy Clin Immunol. 2022 Aug;150(2):406-414.e16. doi: 10.1016/j.jaci.2022.04.023. Epub 2022 Apr 30.
In subjects with systemic mastocytosis, the number of mast cells is elevated many fold. These patients frequently experience unpredictable and recurrent life-threatening mast cell activation (MCA) events.
Our aim was to analyze the derangements of chemokine and cytokine concentrations during severe MCA attacks.
Samples from a patient with indolent systemic mastocytosis were used for this study. A total of 41 chemokines and cytokines were simultaneously measured in triplicate and at multiple time points during 2 severe and 2 moderate MCA events. These were compared to 3 to 5 baseline samples, taken when clinical symptoms were not present.
During the severe MCA event, which required 2 days of treatment in the intensive care unit, peak chemokine (C-C motif) ligand 3, IL-1ra, IL-5, IL-6, IL-10, IL-13, and granulocyte-macrophage colony-stimulating factor concentrations were statistically significantly elevated 29-, 99-, 44-, 280-, 93-, 7-, and 6-fold above baseline, respectively. A highly similar pattern was observed during the second severe MCA event. In the moderate MCA event with PCR-proven influenza A infection, the T1-associated cytokines INF-α, INF-γ, and TNF-α were only statistically significantly elevated 5- to 7-fold above baseline. The correlation coefficients between highly elevated histamine and cytokine concentrations during the acute phase were >95%, indicating the same cellular origin, possibly activated mast cells.
One of the severe MCA events led to life-threatening symptoms over several days. During this event, the massive release of T2 cytokines induced a hyperinflammatory state, fulfilling published criteria for cytokine release syndrome. Administration of IL-6- and IL-5-inhibiting biologicals might significantly shorten the acute phase of severe MCA events, likely offering significant clinical benefits to mastocytosis patients.
在患有系统性肥大细胞增多症的患者中,肥大细胞的数量增加了许多倍。这些患者经常经历不可预测且反复发作的危及生命的肥大细胞激活(MCA)事件。
我们的目的是分析严重 MCA 发作期间趋化因子和细胞因子浓度的紊乱。
本研究使用一位惰性系统性肥大细胞增多症患者的样本。在 2 次严重和 2 次中度 MCA 事件期间,在多个时间点重复测量了 41 种趋化因子和细胞因子,共测量了 3 到 5 次基线样本,这些样本是在没有临床症状时采集的。
在需要在重症监护病房治疗 2 天的严重 MCA 事件中,峰值趋化因子(C-C 基序)配体 3、白细胞介素-1 受体拮抗剂、白细胞介素-5、白细胞介素-6、白细胞介素-10、白细胞介素-13 和粒细胞-巨噬细胞集落刺激因子浓度分别比基线升高了 29 倍、99 倍、44 倍、280 倍、93 倍、7 倍和 6 倍。在第二次严重 MCA 事件中观察到了非常相似的模式。在伴有聚合酶链反应(PCR)证实的甲型流感感染的中度 MCA 事件中,T1 相关细胞因子 IFN-α、IFN-γ 和 TNF-α仅比基线升高了 5 到 7 倍。在急性期中高度升高的组胺和细胞因子浓度之间的相关系数>95%,表明它们具有相同的细胞起源,可能是被激活的肥大细胞。
其中一次严重 MCA 事件导致了数天的危及生命的症状。在此事件中,大量释放的 T2 细胞因子诱导了一种过度炎症状态,符合细胞因子释放综合征的发布标准。施用白细胞介素-6 和白细胞介素-5 抑制性生物制剂可能会显著缩短严重 MCA 事件的急性期,这可能会给肥大细胞增多症患者带来显著的临床益处。