Division of Immunopathology, Department of Pathophysiology and Allergy Research, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Austria.
J Intern Med. 2012 Aug;272(2):144-57. doi: 10.1111/j.1365-2796.2012.02556.x.
Immunoglobulin E-mediated allergies affect more than 25% of the population. Allergen exposure induces a variety of symptoms in allergic patients, which include rhinitis, conjunctivitis, asthma, dermatitis, food allergy and life-threatening systemic anaphylaxis. At present, allergen-specific immunotherapy (SIT), which is based on the administration of the disease-causing allergens, is the only disease-modifying treatment for allergy. Current therapeutic allergy vaccines are still prepared from relatively poorly defined allergen extracts. However, with the availability of the structures of the most common allergen molecules, it has become possible to produce well-defined recombinant and synthetic allergy vaccines that allow specific targeting of the mechanisms of allergic disease. Here we provide a summary of the development and mechanisms of SIT, and then review new forms of therapeutic vaccines that are based on recombinant and synthetic molecules. Finally, we discuss possible allergen-specific strategies for prevention of allergic disease.
免疫球蛋白 E 介导的过敏反应影响超过 25%的人口。过敏原暴露会引起过敏患者的各种症状,包括鼻炎、结膜炎、哮喘、皮炎、食物过敏和危及生命的全身性过敏反应。目前,基于致病过敏原给药的过敏原特异性免疫疗法(SIT)是过敏的唯一一种疾病修正治疗方法。目前的治疗性过敏疫苗仍然是用相对定义不明确的过敏原提取物制备的。然而,随着最常见过敏原分子结构的出现,已经有可能生产出定义明确的重组和合成过敏疫苗,从而可以针对过敏疾病的机制进行特异性靶向。在这里,我们总结了 SIT 的发展和机制,然后回顾了基于重组和合成分子的新型治疗性疫苗。最后,我们讨论了预防过敏疾病的可能的过敏原特异性策略。