Jakob Thilo, Müller Ulrich, Helbling Arthur, Spillner Edzard
aDepartment of Dermatology and Allergology, University Medical Center Gießen (UKGM), Justus-Liebig University Gießen, Giessen, Germany bDepartment of Rheumatology, Immunology and Allergology, University Hospital/Inselspital Bern, Switzerland cImmunological Engineering, Department of Engineering, Aarhus University, Aarhus, Denmark.
Curr Opin Allergy Clin Immunol. 2017 Oct;17(5):363-372. doi: 10.1097/ACI.0000000000000390.
Component-resolved diagnostics makes use of defined allergen molecules to analyse IgE-mediated sensitizations at a molecular level. Here, we review recent studies on the use of component-resolved diagnostics in the field of Hymenoptera venom allergy (HVA) and discuss its benefits and limitations.
Component resolution in HVA has moved from single molecules to panels of allergens. Detection of specific immunoglobulin E (sIgE) to marker and cross-reactive venom allergens has been reported to facilitate the discrimination between primary sensitization and cross-reactivity and thus, to provide a better rationale for prescribing venom immunotherapy (VIT), particularly in patients sensitized to both honeybee and vespid venom. Characterization of IgE reactivity to a broad panel of venom allergens has allowed the identification of different sensitization profiles that in honeybee venom allergy were associated with increased risks for side effects or treatment failure of VIT. In contrast, component resolution so far has failed to provide reliable markers for the discrimination of sensitizations to venoms of different members of Vespidae.
Component-resolved diagnostics allows a better understanding of the complexity of sensitization and cross-reactivities in HVA. In addition, the enhanced resolution and precision may allow identification of biomarkers, which can be used for risk stratification in VIT. Knowledge about the molecular composition of different therapeutic preparations may enable the selection of appropriate preparations for VIT according to individual sensitization profiles, an approach consistent with the goals of personalized medicine.
组分分辨诊断利用特定的过敏原分子在分子水平分析IgE介导的致敏反应。在此,我们综述了近期关于组分分辨诊断在膜翅目毒液过敏(HVA)领域应用的研究,并讨论其利弊。
HVA中的组分分辨已从单一分子发展到过敏原组合。据报道,检测针对标记性和交叉反应性毒液过敏原的特异性免疫球蛋白E(sIgE)有助于区分原发性致敏和交叉反应,从而为开具毒液免疫疗法(VIT)提供更好的理论依据,特别是对于同时对蜜蜂和黄蜂毒液致敏的患者。对广泛的毒液过敏原进行IgE反应性特征分析,已能识别不同的致敏模式,在蜜蜂毒液过敏中,这些模式与VIT副作用风险增加或治疗失败相关。相比之下,到目前为止,组分分辨未能提供可靠的标志物来区分对胡蜂科不同成员毒液的致敏。
组分分辨诊断有助于更好地理解HVA中致敏和交叉反应的复杂性。此外,更高的分辨率和精准度可能有助于识别生物标志物,可用于VIT的风险分层。了解不同治疗制剂的分子组成,可能有助于根据个体致敏模式选择合适的VIT制剂,这一方法符合个性化医疗的目标。