Division of Immunopathology, Department of Pathophysiology and Allergy Research, Center of Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Waehringer Guertel 18-20, A-1090 Vienna, Austria.
Vaccine. 2012 Jun 19;30(29):4328-35. doi: 10.1016/j.vaccine.2011.11.011. Epub 2011 Nov 17.
Hundred years ago therapeutic vaccination with allergen-containing extracts has been introduced as a clinically effective, disease-modifying, allergen-specific and long-lasting form of therapy for allergy, a hypersensitivity disease affecting more than 25% of the population. Today, the structures of most of the disease-causing allergens have been elucidated and recombinant hypoallergenic allergen derivatives with reduced allergenic activity have been engineered to reduce side effects during allergen-specific immunotherapy (SIT). These recombinant hypoallergens have been characterized in vitro, in experimental animal models and in clinical trials in allergic patients. This review provides a summary of the molecular, immunological and preclinical evaluation criteria applied for this new generation of allergy vaccines. Furthermore, we summarize the mechanisms underlying SIT with recombinant hypoallergens which are thought to be responsible for their therapeutic effect.
百年前,含过敏原提取物的治疗性疫苗被引入临床,作为一种针对过敏的疾病修正、过敏原特异性和长效治疗方法,过敏是一种影响超过 25%人群的超敏性疾病。如今,大多数致病过敏原的结构已经阐明,并通过工程设计出具有降低过敏原活性的重组低致敏性过敏原衍生物,以减少过敏原特异性免疫疗法(SIT)期间的副作用。这些重组低致敏原已在体外、实验动物模型和过敏患者的临床试验中进行了表征。本综述概述了应用于新一代过敏疫苗的分子、免疫学和临床前评估标准。此外,我们总结了重组低致敏原 SIT 的作用机制,这些机制被认为是其治疗效果的基础。