Dermatologist and Immunologist, Clinic of Dermatology, Erfurt, Germany.
Allergy. 2011 Jul;66 Suppl 95:41-3. doi: 10.1111/j.1398-9995.2011.02632.x.
Allergen extracts for subcutaneous specific immunotherapy (SCIT) may be adsorbed to aluminium hydroxide for adjuvant effect and to delay allergen discharge. A product with an optimised allergen-to-aluminium hydroxide ratio enables a lower allergen dose and shorter introduction phase. The new therapeutic product Avanz (ALK, Denmark) has an optimised allergen-to-aluminium hydroxide ratio. A multicentre, randomised, phase II clinical trial evaluated the immunological effects and tolerability of two different five-step updosing schedules for Avanz in 400 patients with grass pollen-induced rhinoconjunctivitis with or without asthma, randomised into two groups. Group 1 were administered weekly, and group 2 were administered every 3 to 4 days. After updosing, patients received two maintenance injections after 2 and 4 weeks. In the updosing phase, local and systemic reactions were significantly more frequent in group 2 than group 1. In the maintenance phase, adverse reactions were less common in both groups. No generalised reactions with hypotension or fatal reactions occurred. An increase in allergen-specific immunoglobulin G(4) (IgG(4) ) and IgE antibodies was established one week after the last injection. Avanz is a SCIT product with an optimised allergen-to-aluminium hydroxide ratio that enables a shorter updosing phase. We established an improved safety profile with weekly updosing compared with 3-4-day intervals. Clinical trials are needed to confirm clinical efficacy.
用于皮下特异性免疫治疗 (SCIT) 的过敏原提取物可能会被吸附到氢氧化铝上以增强佐剂作用并延迟过敏原释放。具有最佳过敏原与氢氧化铝比例的产品可以使用更低的过敏原剂量和更短的引入阶段。新型治疗产品 Avanz(ALK,丹麦)具有优化的过敏原与氢氧化铝比例。一项多中心、随机、II 期临床试验评估了 400 例因草花粉引起的鼻结膜炎伴或不伴哮喘的患者使用两种不同五步加量方案的免疫效果和耐受性,这些患者被随机分为两组。第 1 组每周给药,第 2 组每 3-4 天给药。加量后,患者在 2 周和 4 周后接受两次维持注射。在加量阶段,第 2 组比第 1 组更频繁地出现局部和全身反应。在维持阶段,两组不良反应均较少。没有发生低血压或致命反应的全身性反应。最后一次注射后一周,过敏原特异性免疫球蛋白 G(4)(IgG(4))和 IgE 抗体增加。Avanz 是一种具有优化过敏原与氢氧化铝比例的 SCIT 产品,可缩短加量阶段。与 3-4 天间隔相比,我们每周加量的安全性得到了改善。需要临床试验来确认临床疗效。