Scala E
.
Eur Ann Allergy Clin Immunol. 2013 Oct 1;45 Suppl 2:25-32.
Allergen immunotherapy (AIT) represents the only way to modify the natural history of allergic diseases. Unfortunately, AIT is not always followed by a reduction in symptoms. The main reasons for such failure can be inadequate diagnosis and/or the poor treatment. In both cases, an incomplete or insufficient understanding of the component(s) responsible for the IgE sensitization on the one hand, and, on the other hand, the lack of a steady and reliable allergen mixture to be used for the desensitization process, could explain unsuccessful treatment. A more comprehensive IgE reactivity profile evaluation of the patient can be achieved by means of a molecule-based diagnostic approach, in order to distinguish genuine from panallergen-driven antigen recognition. At the same time, a better delineation of AIT products by means of molecular dissection, can allow a stronger correlation between diagnostic findings and immunotherapeutic intervention, thus facilitating the right prescription to the right patient.
变应原免疫疗法(AIT)是改变过敏性疾病自然病程的唯一方法。不幸的是,AIT并非总能使症状减轻。治疗失败的主要原因可能是诊断不充分和/或治疗不当。在这两种情况下,一方面对导致IgE致敏的成分理解不完整或不充分,另一方面缺乏用于脱敏过程的稳定可靠的变应原混合物,都可能解释治疗为何不成功。通过基于分子的诊断方法,可以对患者进行更全面的IgE反应性谱评估,以区分真正的变应原驱动的抗原识别和泛变应原驱动的抗原识别。同时,通过分子剖析更好地界定AIT产品,可以使诊断结果与免疫治疗干预之间建立更强的相关性,从而有助于为合适的患者开具正确的处方。