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基于 CD203c 的嗜碱性粒细胞活化试验在过敏诊断中的特点及与 CD63 上调的差异。

CD203c-based basophil activation test in allergy diagnosis: characteristics and differences to CD63 upregulation.

机构信息

Institute of Experimental and Clinical Pharmacology, Center of Molecular Medicine, Medical University of Graz, Austria.

出版信息

Cytometry B Clin Cytom. 2010 Sep;78(5):308-18. doi: 10.1002/cyto.b.20526. Epub 2010 Apr 14.

Abstract

BACKGROUND

The basophil activation test (BAT) based on CD203c upregulation has been validated as a reliable tool for the diagnosis of IgE-mediated allergies. Nevertheless, CD203c-based BAT is hardly comparable with that of CD63-based tests, as the mechanisms of CD203c versus CD63 induction differ considerably. The aim of the present study was to identify potent influencing factors of the CD203c-based BAT and to emphasize differences between CD63 and CD203c detection.

METHODS

CD203c-based BAT was determined in 82 healthy controls and in 79 allergic patients. The effects of interleukin (IL)-3 and degranulation enhancing substances were investigated and compared with CD63 upregulation. Furthermore, the influence of different storage conditions and incubation times was evaluated and the impact of antiallergic drugs on the test results was assessed.

RESULTS

CD203c and CD63 expression was rapidly upregulated reaching a maximum after 20-30 min. Basophil CD203c upregulation assayed after storage times up to 48 h declined already after 4 h. IL-3 treatment increased CD203c and CD63 baseline levels and decreased basophil CD203c responses in a dose-dependent manner. In contrast, cytochalasin B and latrunculin B did not affect CD203c responses but decreased CD63-based BAT. Finally, therapeutic concentrations of dimetindene and desloratadine did not affect CD203c upregulation.

CONCLUSION

CD203c-based basophil activation test should be performed preferentially within 4 h after taking the blood samples. Priming and degranulation-enhancing factors are not required for CD203c-based BAT. In contrast to skin testing, CD203c-based BAT can be performed in patients undergoing antiallergic treatment. © 2010 International Clinical Cytometry Society.

摘要

背景

基于 CD203c 上调的嗜碱性粒细胞活化试验(BAT)已被验证为 IgE 介导的过敏反应的可靠诊断工具。然而,基于 CD203c 的 BAT 与基于 CD63 的测试几乎无法相比,因为 CD203c 与 CD63 诱导的机制有很大的不同。本研究的目的是确定基于 CD203c 的 BAT 的有力影响因素,并强调 CD63 和 CD203c 检测之间的差异。

方法

在 82 名健康对照者和 79 名过敏患者中确定基于 CD203c 的 BAT。研究了白细胞介素(IL)-3 和脱颗粒增强物质的影响,并与 CD63 上调进行了比较。此外,还评估了不同储存条件和孵育时间的影响,并评估了抗过敏药物对测试结果的影响。

结果

CD203c 和 CD63 的表达迅速上调,在 20-30 分钟后达到最大值。储存时间长达 48 小时后,嗜碱性粒细胞 CD203c 的上调已经在 4 小时后下降。IL-3 处理以剂量依赖的方式增加 CD203c 和 CD63 的基线水平,并降低嗜碱性粒细胞 CD203c 的反应。相比之下,细胞松弛素 B 和拉曲库铵 B 不影响 CD203c 反应,但降低基于 CD63 的 BAT。最后,治疗浓度的二甲替丁和地氯雷他定不影响 CD203c 的上调。

结论

基于 CD203c 的嗜碱性粒细胞活化试验应在采血后 4 小时内进行。基于 CD203c 的 BAT 不需要启动和脱颗粒增强因子。与皮肤测试不同,基于 CD203c 的 BAT 可以在接受抗过敏治疗的患者中进行。© 2010 年国际临床细胞计数学会。

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