Ginsberg David N, Eichenfield Lawrence F
Department of Dermatology, Rady Children's Hospital, San Diego, CA USA.
Department of Dermatology, University of California, San Diego, La Jolla USA ; Division of Dermatology, Rady Children's Hospital, San Diego, CA USA.
World Allergy Organ J. 2016 Apr 18;9:16. doi: 10.1186/s40413-016-0107-2. eCollection 2016.
Atopic dermatitis (AD) is a common chronic skin condition in children that has a proven association with other atopic conditions and allergies. These associations, like the general pathophysiology of AD, are complex and not fully understood. While there is evidence for the efficacy of specific immunotherapy (SIT) in pediatric asthma and allergic rhinitis (AR), there is a lack of strong data to support its use in AD. IgE has been shown to be elevated in many patients with AD, but it is an unreliable biomarker due to variability and great fluctuation over time, poor positive predictive value for clinically relevant allergy, and poor correlation with disease state. In spite of this, almost all studies of SIT use either positive skin prick testing (SPT) or serum specific IgE levels to guide therapy. Allergen avoidance, with some exceptions, is generally not effective at controlling AD in children. The few studies that have investigated the efficacy of SIT in children with AD have produced conflicting results, and a lack of reproducibility with a standard treatment protocol. Limited studies have shown clinical improvement in mild to moderate AD cases, but no effect on more severe patients. Uncontrolled studies are difficult to interpret, due to the natural history of remission or "outgrowing" of AD over time in many patients without specific interventions. Drawbacks to SIT include the length of treatment, poor compliance, cost, and potential side effect profile. The potential for misdirection of time and energy away from skin directed therapy could negatively impact on AD outcomes.
特应性皮炎(AD)是儿童常见的慢性皮肤病,已证实与其他特应性疾病和过敏有关。这些关联,如同AD的一般病理生理学一样,复杂且尚未完全被理解。虽然有证据表明特异性免疫疗法(SIT)对小儿哮喘和过敏性鼻炎(AR)有效,但缺乏有力数据支持其在AD中的应用。许多AD患者的IgE已被证明升高,但由于其随时间的变异性和大幅波动、对临床相关过敏的阳性预测价值低以及与疾病状态的相关性差,它是一种不可靠的生物标志物。尽管如此,几乎所有关于SIT的研究都使用阳性皮肤点刺试验(SPT)或血清特异性IgE水平来指导治疗。除了一些例外情况,避免接触变应原通常对控制儿童AD无效。少数研究特应性皮炎患儿SIT疗效的研究结果相互矛盾,且缺乏标准治疗方案的可重复性。有限的研究表明,轻度至中度AD病例有临床改善,但对重度患者无效。由于许多患者在没有特定干预的情况下AD会随着时间自然缓解或“自愈”,未经对照的研究难以解释。SIT的缺点包括治疗时间长、依从性差、成本高以及潜在的副作用。将时间和精力从针对皮肤的治疗上转移开的可能性可能会对AD的治疗效果产生负面影响。