a Department of Pulmonology , Haematology and Oncology, Division of Pulmonology and Allergology, High Speciality "A.Cardarelli" Hospital , Naples , Italy.
b Postgraduate School of Respiratory Medicine, Department of Experimental Medicine and Surgery , University of Rome "Tor Vergata" , Rome , Italy.
Hum Vaccin Immunother. 2018 Jun 3;14(6):1438-1441. doi: 10.1080/21645515.2018.1434383. Epub 2018 Feb 23.
We hypothesize that a pivotal condition determining the efficacy of dog allergen immunotherapy (DAI) might be the mono-sensitization to dog lipocalins (Can f 1-2) in individuals not directly or indirectly exposed to other furry animals. In fact, the concomitant sensitization to lipocalins and/or albumins, especially in those patients directly exposed to furry animals, may potentially stimulate patient's airways by inducing persistent inflammation and, thus, clinical symptoms. In these conditions, it is likely that DAI alone could be inadequate to reduce airway inflammation mediated by inhalation of dog allergens in patients with simultaneous exposure to other furry animals. Can f 5 has been found as exclusive allergen in about one third of dog-sensitized individuals. Considering the presence of different allergenic materials in extract of mammalian origin, it is evident that a standard DAI is not likely to be effective in Can f 5 prevalent or mono-sensitized individuals. Moreover, we would underline the need of collecting detailed information on the possible exposures to furry animals (other than the common pets), an information that usually is neglected in clinical practice. Furthermore, a detailed clinical history exploring the real significance of dog sensitization (mono or poly-sensitization, induction of clinical symptoms after exposure etc.) should be performed before prescribing DAI. In some patients, with potential high susceptibility to animal allergens, the use of CRD is essential to verify the presence of concomitant allergic sensitization to lipocalins and/or albumins belonging to other furry animals. The availability of CRD introduced the possibility of a better targeted prescription of DAI because it might be useful for point out the primary allergens and for the exclusion of cross-reactive ones.
我们假设,决定狗过敏原免疫治疗(DAI)疗效的关键条件可能是个体对狗脂类结合蛋白(Can f 1-2)的单一过敏,而这些个体没有直接或间接接触其他毛茸茸的动物。事实上,同时对脂类结合蛋白和/或白蛋白过敏,尤其是那些直接接触毛茸茸动物的患者,可能会通过诱导持续炎症和临床症状来刺激患者的气道。在这些情况下,单独使用 DAI 可能不足以减少同时暴露于其他毛茸茸动物的患者吸入狗过敏原引起的气道炎症。Can f 5 已被发现是约三分之一狗致敏个体的特有过敏原。考虑到哺乳动物来源提取物中存在不同的过敏原物质,很明显,标准的 DAI 不太可能对 Can f 5 流行或单一过敏个体有效。此外,我们强调需要收集有关可能接触毛茸茸动物(除常见宠物外)的详细信息,这些信息通常在临床实践中被忽视。此外,在开具 DAI 之前,应进行详细的临床病史调查,以探索狗过敏的真正意义(单一或多种过敏、暴露后引发临床症状等)。在某些具有高动物过敏原易感性的患者中,使用 CRD 至关重要,以验证是否存在对其他毛茸茸动物的脂类结合蛋白和/或白蛋白的同时过敏。CRD 的可用性引入了更好地靶向 DAI 处方的可能性,因为它可能有助于确定主要过敏原并排除交叉反应性过敏原。