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A method for treating allergic disease and asthma by recombinant adenovirus-and adeno-associated virus-mediated ifn-gamma gene

机译:重组腺病毒和腺相关病毒介导的ifn-γ基因治疗过敏性疾病和哮喘的方法

摘要

The subject invention concerns an effective therapy for asthma, including allergic disease, using cytokine gene expression therapy. The subject invention further pertains to the use of adenovirus-mediated IFN-Ϝ (Ad-IFN-Ϝ) gene transfer to prevent or treat allergic disease and asthma, including associated conditions such as allergen-induced airway inflammation and airway hyperresponsiveness. The subject invention includes a method for effectively attenuating allergen-induced airway inflammation and airway hyperresponsiveness by administering to the respiratory tract Ad-IFN-Ϝ, to affect IL-12 and STAT-4 levels. The subject invention also provides compositions for gene therapy for asthma by the transfer of IFN-Ϝ
机译:本发明涉及使用细胞因子基因表达疗法来治疗包括过敏性疾病的哮喘的有效疗法。本发明进一步涉及腺病毒介导的IFN-γ(Ad-IFN-γ)基因转移在预防或治疗变应性疾病和哮喘中的用途,包括相关条件,例如变应原诱导的气道炎症和气道高反应性。本发明包括通过对呼吸道施用Ad-IFN-γ以影响IL-12和STAT-4水平来有效减轻变应原诱导的气道炎症和气道高反应性的方法。本发明还提供了通过转移IFN-γ进行哮喘的基因治疗的组合物

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