Metz-Favre Carine, Linhart Birgit, Focke-Tejkl Margarete, Purohit Ashok, de Blay Frédéric, Valenta Rudolf, Pauli Gabrielle
Department of Respiratory Diseases, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
J Allergy Clin Immunol. 2007 Aug;120(2):315-21. doi: 10.1016/j.jaci.2007.03.046. Epub 2007 May 23.
A recombinant hybrid molecule (HM) consisting of 4 major allergens from timothy grass (Phl p 1, 2, 5, and 6) was expressed in Escherichia coli, purified, and characterized regarding its immunologic properties.
We sought to determine whether the recombinant HM can be used for the diagnosis of grass pollen allergy by means of skin testing.
Skin prick testing was performed in 32 patients with grass pollen allergy and in 9 control individuals by using increasing concentrations (4, 12, 36, and 108 mug/mL) of the HM and using commercial grass pollen extract. Specific IgE reactivities against the HM, grass pollen extract, and a panel of purified grass pollen allergens (recombinant Phl p 1, 2, 5, 6, 7, 12, and 13 and natural Phl p 4) were measured by means of ELISA, and timothy grass pollen-specific IgE levels were determined by using ImmunoCAP.
Grass pollen allergy was diagnosed in all patients by means of skin testing with the HM. No false-positive skin test responses were obtained in the control individuals. There was an excellent correlation between IgE levels obtained with the HM and natural grass pollen extract measured by means of ELISA (r = 0.98, P < .0001) and by means of ImmunoCAP (r = 0.98, P < .0001).
The recombinant HM permitted accurate and specific in vivo diagnosis of grass pollen allergy in all tested patients. It can be considered a well-defined tool for the diagnosis and perhaps for immunotherapy of grass pollen allergy.
A recombinant HM can replace traditional allergen extracts for skin test-based diagnosis of grass pollen allergy.
一种由梯牧草的4种主要变应原(Phl p 1、2、5和6)组成的重组杂交分子(HM)在大肠杆菌中表达、纯化,并对其免疫特性进行了表征。
我们试图确定重组HM是否可用于通过皮肤试验诊断草花粉过敏。
对32例草花粉过敏患者和9名对照个体进行皮肤点刺试验,使用浓度递增的HM(4、12、36和108μg/mL)以及市售草花粉提取物。通过酶联免疫吸附测定(ELISA)测量针对HM、草花粉提取物和一组纯化的草花粉变应原(重组Phl p 1、2、5、6、7、12和13以及天然Phl p 4)的特异性IgE反应性,并使用免疫捕获法(ImmunoCAP)测定梯牧草花粉特异性IgE水平。
通过使用HM进行皮肤试验,所有患者均被诊断为草花粉过敏。对照个体未出现假阳性皮肤试验反应。通过ELISA(r = 0.98,P <.0001)和ImmunoCAP(r = 0.98,P <.0001)测量,HM与天然草花粉提取物的IgE水平之间存在极好的相关性。
重组HM允许对所有受试患者进行准确且特异的草花粉过敏体内诊断。它可被视为草花粉过敏诊断以及可能的免疫治疗的一种明确工具。
重组HM可替代传统变应原提取物用于基于皮肤试验的草花粉过敏诊断。