Hassani Marwan, Tak Tamar, van Aalst Corneli, van Nederveen Saar, Tesselaar Kiki, Vrisekoop Nienke, Koenderman Leo
Center for Translational Immunology, University Medical Center Utrecht, Heidelberglaan 100, 3584CX Utrecht, The Netherlands.
Department of Respiratory Medicine, University Medical Center Utrecht, Heidelberglaan 100, 3584CX Utrecht, The Netherlands.
iScience. 2021 Jul 28;24(8):102913. doi: 10.1016/j.isci.2021.102913. eCollection 2021 Aug 20.
Mepolizumab (anti-IL-5) is a successful biological for treatment of T2/eosinophilic asthma by blocking the IL-5-eosinophil axis. The kinetics of human eosinophils in blood and sputum was determined to better understand the underlying mechanism(s). Pulse-chase labeling was performed with 6,6-H-glucose in patients with asthma after short term (4 days) and long term (84 days) treatment with mepolizumab (n = 10) or placebo (n = 10). The retention time of eosinophils in sputum was longer than in blood. Treatment with mepolizumab induced a fast and long-lasting eosinopenia with no reduction of eosinophil progenitors. The retention time of eosinophils in blood was delayed only after short-term treatment. This leads to the hypothesis that IL-5 increases the number of progenitors and potentiates homing to the tissues, leading to reactive eosinophilia. Long-term treatment is associated with low numbers of IL-5-independent eosinophils in blood and tissues. Therefore, long-term treatment with mepolizumab restores the kinetics of eosinophils as normally found in homeostasis.
美泊利单抗(抗白细胞介素-5)是一种通过阻断白细胞介素-5-嗜酸性粒细胞轴来治疗2型/嗜酸性粒细胞性哮喘的成功生物制剂。为了更好地理解潜在机制,对血液和痰液中的人类嗜酸性粒细胞动力学进行了测定。在短期(4天)和长期(84天)接受美泊利单抗(n = 10)或安慰剂(n = 10)治疗的哮喘患者中,用6,6-H-葡萄糖进行脉冲追踪标记。嗜酸性粒细胞在痰液中的滞留时间比在血液中更长。美泊利单抗治疗可诱导快速且持久的嗜酸性粒细胞减少,而嗜酸性粒细胞祖细胞数量无减少。仅在短期治疗后,嗜酸性粒细胞在血液中的滞留时间才延迟。这导致了一种假设,即白细胞介素-5增加祖细胞数量并增强向组织的归巢,导致反应性嗜酸性粒细胞增多。长期治疗与血液和组织中白细胞介素-5非依赖性嗜酸性粒细胞数量低有关。因此,美泊利单抗长期治疗可恢复稳态中正常的嗜酸性粒细胞动力学。