Department of Clinical Sciences, Intervention and Technology, Division of ENT Diseases, Karolinska Institutet, Stockholm, Sweden.
J Allergy Clin Immunol. 2013 Feb;131(2):412-20. doi: 10.1016/j.jaci.2012.10.056.
Allergen-specific immunotherapy is the only causative treatment of IgE-mediated allergic disorders. The most common administration route is subcutaneous, which may necessitate more than 50 allergen injections during 3 to 5 years. Recent evidence suggests that direct intralymphatic injections could yield faster beneficial results with considerably lower allergen doses and markedly reduced numbers of injections.
To evaluate the effects of intralymphatic allergen-specific immunotherapy in pollen-allergic patients.
In an open pilot investigation followed by a double-blind, placebo-controlled study, patients with allergic rhinitis were treated with 3 intralymphatic inguinal injections of ALK Alutard (containing 1000 SQ-U birch pollen or grass pollen) or placebo (ALK diluent). Clinical pre- and posttreatment parameters were assessed, the inflammatory cell content in nasal lavage fluids estimated, and the activation pattern of peripheral T cells described.
All patients tolerated the intralymphatic immunotherapy (ILIT) treatment well, and the injections did not elicit any severe adverse event. Patients receiving active treatment displayed an initial increase in allergen-specific IgE level and peripheral T-cell activation. A clinical improvement in nasal allergic symptoms upon challenge was recorded along with a decreased inflammatory response in the nose. In addition, these patients reported an improvement in their seasonal allergic disease. No such changes were seen in the placebo group.
Although this study is based on a limited number of patients, ILIT with grass-pollen or birch-pollen extracts appears to reduce nasal allergic symptoms without causing any safety problems. Hence, ILIT might constitute a less time-consuming and more cost-effective alternative to conventional subcutaneous allergen-specific immunotherapy.
变应原特异性免疫疗法是 IgE 介导的过敏性疾病的唯一病因治疗方法。最常见的给药途径是皮下给药,但在 3 至 5 年内可能需要进行 50 多次过敏原注射。最近的证据表明,直接淋巴管内注射可以用更少的过敏原剂量和明显减少的注射次数更快地产生有益的结果。
评估花粉过敏患者进行淋巴管内变应原特异性免疫治疗的效果。
在一项开放的初步研究之后,进行了一项双盲、安慰剂对照研究,对变应性鼻炎患者进行 3 次腹股沟内淋巴管内注射 ALK Alutard(含 1000 SQ-U 桦树花粉或草花粉)或安慰剂(ALK 稀释剂)。评估治疗前后的临床参数,估计鼻灌洗液中的炎症细胞含量,并描述外周 T 细胞的激活模式。
所有患者均耐受淋巴管内免疫治疗(ILIT),且注射未引起任何严重不良反应。接受主动治疗的患者表现出初始过敏原特异性 IgE 水平和外周 T 细胞激活增加。在挑战时记录到鼻过敏症状的临床改善,并伴有鼻腔炎症反应的降低。此外,这些患者报告他们的季节性过敏性疾病得到改善。安慰剂组未观察到这些变化。
尽管这项研究基于有限数量的患者,但草花粉或桦树花粉提取物的 ILIT 似乎可以减轻鼻过敏症状,而不会引起任何安全问题。因此,ILIT 可能是一种比传统皮下变应原特异性免疫治疗更省时、更具成本效益的替代方法。