Şahin Ethem, Bafaqeeh Sameer Ali, Güven Selis Gülseven, Çetinkaya Erdem Atalay, Muluk Nuray Bayar, Coşkun Zerrin Ozergin, Lopatin Andrey, Kar Murat, Pinarbasli Mehmet Ozgur, Cingi Cemal
Ear, Nose and Throat (ENT) Clinics; Bayındır Içerenköy Hospital, Istanbul, Turkey.
Am J Rhinol Allergy. 2016 Sep 1;30(5):1-3. doi: 10.2500/ajra.2016.30.4367.
Allergen immunotherapy (AIT) leads to the production of antiallergen immunoglobulin (IgG) or "blocking antibody" in the serum and an increase in antiallergen IgG and IgA in nasal secretions. There is also a decrease in the usual rise in antiallergen IgE that occurs after the pollen season.
In this paper, mechanisms of action of allergen immunotherapy is reviewed.
Regulatory T (Treg) cells and their cytokines, primarily interleukin (IL) 10 and transforming growth factor beta, suppress T-helper type 2 immune responses and control allergic diseases in many ways. AIT induces a shift in the proportion of IL-4-secreting T-helper type 2 cells in favor of IL-10-secreting inducible Treg cells specific for the same allergenic epitope that increases in number and function. Different types of inducible Treg control several facets of allergic inflammation. There are two main types of immunotherapy: subcutaneous immunotherapy and sublingual immunotherapy. Subcutaneous immunotherapy is efficacious and is indicated for the reduction of seasonal symptoms. Sublingual immunotherapy involves the regular self-administration and retention of allergen extract under the tongue for 1-2 minutes before the extract is swallowed. The allergens cross the mucosa in 15-30 minutes and are then captured by tolerogenic dendritic cells and processed as small peptides. Next, via the lymphatic system, a systemic immune response is created to produce an early decrease in mast cell and basophil degranulation.
AIT is indicated for the treatment of moderate-to-severe intermittent or persistent symptoms of allergic rhinitis. AIT can be administered to those >5 years of age and has been shown to be safe in children as young as 3 years of age. In this article, AIT and other types of immunotherapies were discussed as well as the indications for immunotherapy.
变应原免疫疗法(AIT)可导致血清中产生抗变应原免疫球蛋白(IgG)或“封闭抗体”,并使鼻分泌物中的抗变应原IgG和IgA增加。花粉季节后通常出现的抗变应原IgE升高也会降低。
本文综述了变应原免疫疗法的作用机制。
调节性T(Treg)细胞及其细胞因子,主要是白细胞介素(IL)-10和转化生长因子β,以多种方式抑制2型辅助性T细胞免疫反应并控制过敏性疾病。AIT诱导分泌IL-4的2型辅助性T细胞比例发生变化,有利于分泌IL-10的、针对相同变应原表位的诱导性Treg细胞,其数量和功能均增加。不同类型的诱导性Treg控制过敏性炎症的多个方面。免疫疗法主要有两种类型:皮下免疫疗法和舌下免疫疗法。皮下免疫疗法有效,适用于减轻季节性症状。舌下免疫疗法是指在吞咽变应原提取物前,将其在舌下定期自行给药并保留1 - 2分钟。变应原在15 - 30分钟内穿过黏膜,然后被耐受性树突状细胞捕获并加工成小肽。接下来,通过淋巴系统产生全身免疫反应,使肥大细胞和嗜碱性粒细胞脱颗粒早期减少。
AIT适用于治疗中重度间歇性或持续性过敏性鼻炎症状。AIT可用于5岁以上人群,且已证明对3岁幼儿也安全。本文讨论了AIT和其他类型的免疫疗法以及免疫疗法的适应证。