[New experimental therapies for type I allergy].

Immunitat und Infektion Pub Date : 1994-06-01
H Renz
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Abstract

CD4+ T cells play a central role in the development of the immediate-type allergic response. It was shown that T cells from allergic patients exhibit an imbalance on the level of cytokine production which is characterized by increased IL-4- and decreased IFN-gamma production. Different strategies were developed to therapeutically interfere on various levels of the immunological dysregulation. In this article, the use of the immunomodulatory and immunosuppressive drugs methotrexate, cyclosporine, and intravenous immunoglobulin (IVIG) will be discussed. Furthermore, new experimental therapeutic approaches will be presented which are aimed to selectively interfere on the level of cytokine production and regulation. A different approach targets the functional activity of allergen-specific T cells whose functions could be modulated in an animal model system by subcutaneous treatment with peptides.

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[I型过敏的新实验疗法]。
CD4+ T细胞在立即型过敏反应的发展中起核心作用。研究表明,过敏患者的T细胞在细胞因子产生水平上表现出不平衡,其特征是IL-4-增加和ifn - γ产生减少。不同的策略被开发用于治疗干预不同水平的免疫失调。本文将讨论免疫调节和免疫抑制药物甲氨蝶呤、环孢素和静脉注射免疫球蛋白(IVIG)的使用。此外,新的实验治疗方法将被提出,旨在选择性地干扰细胞因子的产生和调节水平。另一种不同的方法是针对过敏原特异性T细胞的功能活性,其功能可以在动物模型系统中通过皮下治疗肽来调节。
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