Clinical Trials Center, Center for Clinical Research, University and University Hospital of Zurich, Rämistrasse 100, 8091 Zurich, Switzerland.
Curr Top Microbiol Immunol. 2011;352:71-84. doi: 10.1007/82_2011_133.
Allergen specific immunotherapy (SIT) is the only treatment of IgE mediated allergies that is causative and has a long-term effect. Classically, SIT requires numerous subcutaneous injections of the allergen during 3-5 years. Over the last decade sublingual allergen applications have established as an alternative, but treatment duration could not be shortened. This review focuses on direct administration of vaccines in general and of allergens in particular into lymph nodes with the aim to enhance immunotherapy. Several studies have found that direct injection of antigens into lymph nodes enhanced immune responses. Recently we have focused on intralymphatic allergen administration in order to enhance SIT. Data in mouse models and in clinical trials showed that intralymphatic allergen administration strongly enhanced SIT, so that the number of allergen injections could be reduced to three, and the allergen dose could be reduced 10-100 fold. Intralymphatic injections proved easy, practically painless and safe. In mice and men, intralymphatic immunotherapy injecting allergens into a subcutaneous lymph node markedly enhances the protective immune response, so that both the dose and number of allergen injections can be reduced, making SIT safer and faster, which enhances patient convenience and compliance.
变应原特异性免疫治疗(SIT)是唯一针对 IgE 介导的过敏反应的病因治疗方法,具有长期疗效。传统上,SIT 需要在 3-5 年内进行多次皮下注射过敏原。在过去的十年中,舌下过敏原应用已经确立为一种替代方法,但治疗时间无法缩短。本综述重点介绍了将疫苗,特别是过敏原直接施用于淋巴结,以增强免疫治疗。多项研究发现,直接将抗原注射到淋巴结中可增强免疫反应。最近,我们专注于淋巴管内过敏原给药,以增强 SIT。在小鼠模型和临床试验中的数据表明,淋巴管内过敏原给药可显著增强 SIT,从而将过敏原注射次数减少至 3 次,并且过敏原剂量可减少 10-100 倍。淋巴管内注射证明是简单,几乎无痛且安全的。在小鼠和人类中,将过敏原注入皮下淋巴结的淋巴管内免疫疗法可显著增强保护性免疫反应,从而减少过敏原注射的剂量和次数,使 SIT 更安全,更快,从而提高患者的便利性和依从性。