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伴有显著嗜酸性粒细胞增多或肥大细胞增多症患者的白细胞介素-5 受体α水平。

IL-5 receptor α levels in patients with marked eosinophilia or mastocytosis.

机构信息

Laboratory of Allergic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Md.

出版信息

J Allergy Clin Immunol. 2011 Nov;128(5):1086-92.e1-3. doi: 10.1016/j.jaci.2011.05.032. Epub 2011 Jul 16.

Abstract

BACKGROUND

IL-5 plays a central role in the development and maintenance of eosinophilia (EO) and eosinophil activation in a wide variety of eosinophilic disorders. Although IL-5, IL-3, and GM-CSF can modulate the expression of IL-5 receptor α (IL-5Rα) on eosinophils in vitro, little is known about soluble and surface IL-5Rα levels in vivo.

OBJECTIVE

To assess soluble and surface IL-5Rα levels in patients with EO and/or mastocytosis.

METHODS

Surface IL-5Rα expression was assessed by flow cytometry in blood and/or bone marrow from subjects with EO (n = 39) and systemic mastocytosis (n = 8) and from normal volunteers (n = 28). Soluble IL-5Rα (sIL-5Rα) level was measured in a cohort of 177 untreated subjects and correlated with EO, eosinophil activation, and serum tryptase and cytokine levels.

RESULTS

IL-5Rα expression on eosinophils inversely correlated with EO (r = -0.48; P < .0001), whereas serum levels of sIL-5Rα increased with the eosinophil count (r = 0.56; P < .0001) and serum IL-5 (r = 0.40; P < .0001) and IL-13 (r = 0.29; P = .004) levels. Of interest, sIL-5Rα level was significantly elevated in patients with systemic mastocytosis without EO. Although sIL-5Rα levels correlated with serum tryptase levels in these patients, eosinophil activation, assessed by CD69 expression on eosinophils and serum eosinophil-derived neurotoxin levels, was increased compared with that in normal subjects.

CONCLUSIONS

These data are consistent with an in vivo IL-5Rα regulatory pathway in human eosinophils similar to that described in vitro and involving a balance between soluble and surface receptor levels. This may have implications with respect to the use of novel therapeutic agents targeting IL-5 and its receptor in patients with EO and/or mastocytosis.

摘要

背景

白细胞介素 5(IL-5)在各种嗜酸性粒细胞增多症和嗜酸性粒细胞激活疾病中发挥核心作用,调节嗜酸性粒细胞的发展和维持。虽然白细胞介素 5、白细胞介素 3 和粒细胞-巨噬细胞集落刺激因子(GM-CSF)可以在体外调节嗜酸性粒细胞上的白细胞介素 5 受体α(IL-5Rα)的表达,但体内可溶性和表面 IL-5Rα 水平知之甚少。

目的

评估嗜酸性粒细胞增多症和/或肥大细胞增多症患者的可溶性和表面 IL-5Rα 水平。

方法

通过流式细胞术评估血液和/或骨髓中嗜酸性粒细胞增多症(n = 39)和系统性肥大细胞增多症(n = 8)患者以及正常志愿者(n = 28)的表面 IL-5Rα 表达。在未经治疗的 177 例患者队列中测量可溶性 IL-5Rα(sIL-5Rα)水平,并与嗜酸性粒细胞、嗜酸性粒细胞活化以及血清胰蛋白酶和细胞因子水平相关。

结果

嗜酸性粒细胞上的 IL-5Rα 表达与嗜酸性粒细胞增多呈负相关(r = -0.48;P <.0001),而血清 sIL-5Rα 水平随嗜酸性粒细胞计数增加而增加(r = 0.56;P <.0001),与血清白细胞介素 5(r = 0.40;P <.0001)和白细胞介素 13(r = 0.29;P =.004)水平相关。有趣的是,在无嗜酸性粒细胞增多症的系统性肥大细胞增多症患者中,sIL-5Rα 水平显著升高。尽管这些患者的 sIL-5Rα 水平与血清胰蛋白酶水平相关,但与正常受试者相比,通过嗜酸性粒细胞上的 CD69 表达和血清嗜酸性粒细胞衍生神经毒素水平评估的嗜酸性粒细胞活化增加。

结论

这些数据与体外描述的人类嗜酸性粒细胞中 IL-5Rα 的体内调节途径一致,涉及可溶性和表面受体水平之间的平衡。这可能对在嗜酸性粒细胞增多症和/或肥大细胞增多症患者中使用新型靶向白细胞介素 5 和其受体的治疗药物具有重要意义。

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