Hitting the mucosal road in tolerance induction.

Ursula Wiedermann
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引用次数: 3

Abstract

Within the last decades a dramatic increase in allergic diseases has been recognized in the Westernized societies, leading to the fact that meanwhile 25-30% of the population is afflicted by allergic disorders. Besides a hereditary disposition, other factors, including a reduced microbial contact early in life or changes in nutrition, might also have influenced this epidemiological development. So far the only causative treatment against type-I allergies is specific immunotherapy. In young and monosensitized patients this treatment is highly efficacious, while there are clear limitations in older or multisensitized patients. Allergy research therefore aims at establishing new and more efficacious treatment strategies in prophylactic as well as therapeutic settings. Our research programs focus on the development of novel allergy vaccines based on the induction of mucosal tolerance. In different mouse models of respiratory allergy mucosal treatment with genetically engineered allergen constructs proved to prevent the development of allergic mono- and multisensitivities. The additional use of mucosal adjuvants seems particularly important to improve therapeutic treatment approaches. Recent studies on the inverse relation of certain parasite infections and the development of allergy prompted us to search for selected parasitic molecules with immunosuppressive properties as potential adjuvant systems for novel allergy vaccines. An overview of our recent studies will be given.

在耐受诱导中击中粘膜路。
在过去的几十年里,在西方化的社会中,过敏性疾病急剧增加,导致25-30%的人口受到过敏性疾病的折磨。除了遗传倾向外,其他因素,包括生命早期微生物接触减少或营养变化,也可能影响这种流行病学的发展。到目前为止,针对i型过敏的唯一治疗方法是特异性免疫疗法。在年轻和单致敏的患者中,这种治疗非常有效,而在老年或多致敏的患者中有明显的局限性。因此,过敏研究的目的是在预防和治疗环境中建立新的和更有效的治疗策略。我们的研究重点是基于诱导粘膜耐受的新型过敏疫苗的开发。在不同的呼吸道过敏小鼠模型中,用基因工程过敏原构建的粘膜治疗被证明可以防止过敏性单和多敏感性的发展。粘膜佐剂的额外使用似乎对改善治疗方法特别重要。最近对某些寄生虫感染与过敏发展的反比关系的研究促使我们寻找具有免疫抑制特性的寄生虫分子作为新型过敏疫苗的潜在佐剂系统。将概述我们最近的研究。
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