首页> 外国专利> BIOLOGICAL VARIABILITY OF ASTHMA ASSOCIATED FACTOR 2 AAF2 (IL-9 RECEPTOR) USEFUL FOR THE TREATMENT AND DIAGNOSIS OF ATOPIC ALLERGIES SUCH AS ASTHMA AND ASTHMA-RELATED ILLNESSES

BIOLOGICAL VARIABILITY OF ASTHMA ASSOCIATED FACTOR 2 AAF2 (IL-9 RECEPTOR) USEFUL FOR THE TREATMENT AND DIAGNOSIS OF ATOPIC ALLERGIES SUCH AS ASTHMA AND ASTHMA-RELATED ILLNESSES

机译:哮喘相关因子2 AAF2(IL-9受体)的生物学变异性,可用于哮喘和哮喘相关疾病的治疗和诊断

摘要

This invention relates to the diagnosis, treatment and methods for discovery of new therapeutics for atopic asthma and related disorders based on variants of Asthma Associated Factor (2). One embodiment of the invention is a variant of AAF2, wherein codon 173 is deleted resulting in the loss of glutamine 173 from the mature protein precursor. This single amino acid deletion results in a non-functional AAF2 protein and therefore the presence of this phenotype should be associated with less evidence of atopic asthma. Correspondingly, the lack of susceptibility to an asthmatic, atopic phenotype is characterized by the loss of glutamine at codon 173. The invention includes isolated DNA molecules which are variants of the wild type sequence as well as the proteins encoded by such DNA and the use of such DNA molecules and expressed protein in the diagnosis and treatment of atopic asthma.
机译:本发明涉及基于哮喘相关因子(2)的变体发现用于特应性哮喘和相关疾病的新疗法的诊断,治疗和方法。本发明的一个实施方案是AAF2的变体,其中密码子173被缺失,导致谷氨酰胺173从成熟蛋白前体中丢失。该单个氨基酸缺失导致无功能的AAF2蛋白,因此,该表型的存在与特应性哮喘的证据较少相关。相应地,对哮喘,特应性表型缺乏敏感性的特征在于密码子173处谷氨酰胺的丢失。本发明包括作为野生型序列的变体的分离的DNA分子以及由这种DNA编码的蛋白质,以及使用这类DNA分子和表达的蛋白质在特应性哮喘的诊断和治疗中。

著录项

  • 公开/公告号AT471982T

    专利类型

  • 公开/公告日2010-07-15

    原文格式PDF

  • 申请/专利权人 GENAERA CORPORATION;

    申请/专利号AT20040013403T

  • 申请日1997-12-02

  • 分类号C12N15/09;C12N15/12;A61K38;A61K38/17;A61P11/06;C07K14/715;C12N5/10;C12N15/11;C12Q1/68;G01N33/566;G01N33/68;

  • 国家 AT

  • 入库时间 2022-08-21 18:43:41

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