Vachová Martina, Panzner Petr, Vlas Tomáš, Vítovcová Petra
Department of Immunology and Allergology, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czechia,
Department of Immunology and Allergology, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czechia.
Int Arch Allergy Immunol. 2020;181(4):278-284. doi: 10.1159/000505518. Epub 2020 Feb 4.
Frequently observed multiple sensitizations to several animals highlights the importance of a molecular diagnosis, distinguishing between sensitizations specific to single species and sensitizations due to cross-reactivity.
The aim of our study was to assess the usefulness of a molecular diagnosis in the description of sensitization profiles in allergy patients living in Central Europe, with a particular focus on animal-derived molecules.
The molecular diagnosis was performed using the ImmunoCAP ISAC microarray. Results of 1,255 allergy patients were subjected to statistical analysis.
The highest sensitization rates were observed for uteroglobin Fel d 1 (31.8%) and kallikrein Can f 5 (16.4%), followed by animal lipocalins Can f 1 (13.9%), Equ c 1 (6.2%), Fel d 4 (5.3%), Can f 2 (4.2%), and Mus m 1 (4.1%). Sensitization rates to serum albumins Fel d 2, Can f 3, Equ c 3, and Bos d 6 were very low, with the highest being 3.2% to Fel d 2. Detailed subanalysis confirmed the dominant role of Fel d 1 or Can f 5 and/or Can f 1 in cat- or dog-sensitized patients, respectively. Further analysis focused on lipocalins and albumins confirmed a high rate of cosensitizations within both groups.
The sensitization to animal allergen molecules is very frequent in Central Europe. The most common is sensitization to species-specific cat uteroglobin Fel d 1 and dog kallikrein Can f 5, followed by sensitizations to animal lipocalins. Our data suggest that commonly observed multiple sensitizations detected by extract approach can be explained not only by true cosensitization, but also by cross-reactivity, mainly in the frame of lipocalins. Cross-reactive serum albumins are minor sensitizers and are probably not important from this point of view.
经常观察到对多种动物的多重致敏现象突出了分子诊断的重要性,即区分对单一物种的特异性致敏和交叉反应引起的致敏。
我们研究的目的是评估分子诊断在描述中欧过敏患者致敏谱方面的实用性,特别关注动物源性分子。
使用ImmunoCAP ISAC微阵列进行分子诊断。对1255例过敏患者的结果进行统计分析。
观察到子宫珠蛋白Fel d 1(31.8%)和激肽释放酶Can f 5(16.4%)的致敏率最高,其次是动物脂质运载蛋白Can f 1(13.9%)、Equ c 1(6.2%)、Fel d 4(5.3%)、Can f 2(4.2%)和Mus m 1(4.1%)。对血清白蛋白Fel d 2、Can f 3、Equ c 3和Bos d 6的致敏率非常低,其中对Fel d 最 高为3.2%。详细的亚分析证实了Fel d 1或Can f 5和/或Can f 1分别在猫或狗致敏患者中的主导作用。对脂质运载蛋白和白蛋白的进一步分析证实了两组中共同致敏的高发生率。
在中欧,对动物过敏原分子的致敏非常常见。最常见的是对物种特异性的猫子宫珠蛋白Fel d 1和狗激肽释放酶Can f 5的致敏,其次是对动物脂质运载蛋白的致敏。我们的数据表明,通过提取物方法检测到的常见多重致敏现象不仅可以用真正的共同致敏来解释,还可以用交叉反应来解释,主要是在脂质运载蛋白的范围内。交叉反应性血清白蛋白是次要的致敏原,从这个角度来看可能并不重要。