Allergy Partners, PA, Asheville, North Carolina, USA.
Ann Allergy Asthma Immunol. 2011 Nov;107(5):441-7. doi: 10.1016/j.anai.2011.06.026. Epub 2011 Aug 5.
Subcutaneous allergen-specific immunotherapy is a proven, highly effective treatment for immunoglobulin E-mediated diseases. Despite its proven benefits, only a small percentage of patients with allergic disease use immunotherapy, in part because of the inconvenience associated with treatment. Cluster allergen immunotherapy may offer patients a more convenient treatment option but is prescribed infrequently because of the perception that accelerated immunotherapy buildup leads a higher rate of systemic reactions.
To examine the safety of cluster immunotherapy and identify risk factors for systemic reactions during cluster buildup.
A retrospective, observational review in a large, multicenter allergy practice group was conducted for patients receiving cluster immunotherapy between May 2008 and October 2010.
Data from 441 patients receiving cluster immunotherapy were collected. Forty-eight patients (10.9%) experienced systemic reactions. Based on the World Allergy Organization Subcutaneous Immunotherapy Systemic Reaction Grading System, 18 grade 1 reactions (38.3%), 23 grade 2 reactions (48.9%), 5 grade 3 reactions (10.6%), 1 grade 4 reaction (2.1%), and no grade 5 reactions were seen. Risk factors for a systemic reaction included: female sex, physician diagnosis of asthma, age 21 to 40 years, and inclusion of certain allergens in the immunotherapy vaccine.
Cluster immunotherapy allows patients to reach their immunotherapy maintenance dose more rapidly and may lead to more rapid symptomatic improvement. However, the cluster buildup may lead to a higher rate of systemic reactions. Identifying risk factors for systemic reactions will help improve the safety of cluster immunotherapy.
皮下变应原特异性免疫疗法是一种已被证实的、高度有效的 IgE 介导疾病治疗方法。尽管已证实其具有益处,但仅有一小部分过敏性疾病患者使用免疫疗法,部分原因是治疗相关的不便。集群变应原免疫疗法可为患者提供更便捷的治疗选择,但由于人们认为加速免疫疗法积累会导致更高的全身性反应发生率,因此该疗法的应用并不广泛。
检查集群免疫疗法的安全性,并确定集群积累过程中全身性反应的危险因素。
对 2008 年 5 月至 2010 年 10 月期间在大型多中心过敏实践组中接受集群免疫疗法的患者进行回顾性、观察性研究。
共收集了 441 名接受集群免疫疗法的患者的数据。48 名患者(10.9%)出现全身性反应。根据世界过敏组织皮下免疫治疗全身性反应分级系统,18 例为 1 级反应(38.3%),23 例为 2 级反应(48.9%),5 例为 3 级反应(10.6%),1 例为 4 级反应(2.1%),无 5 级反应。全身性反应的危险因素包括:女性、医生诊断为哮喘、年龄在 21 至 40 岁之间以及免疫疗法疫苗中包含某些过敏原。
集群免疫疗法可使患者更快地达到免疫疗法维持剂量,并可能导致更快的症状改善。然而,集群积累可能会导致更高的全身性反应发生率。确定全身性反应的危险因素将有助于提高集群免疫疗法的安全性。