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Allergen???Fc-gamma1 proteins to treat food allergy

Allergen???Fc-gamma1 proteins to treat food allergy
过敏原???Fc-gamma1蛋白治疗食物过敏
批准号:
7807490
负责人:
ANDREW SAXON
金额:
$17.24万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-06-01 至 2011-05-31

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中文摘要
翻译
描述(由申请人提供):本提案的目标是开发一种新的过敏原特异性免疫疗法并将其商业化,作为严重食物过敏的治疗方法。食物过敏影响了约3.5%的美国人口和6%至8%的幼儿。这显然是在上升。花生过敏影响了大约1%的人口,是最严重的食物过敏之一,每年导致3万急诊室就诊,200多人死亡。标准的基于过敏原蛋白的脱敏疗法--用于过敏性呼吸道疾病的免疫疗法--已被证明不成功,而且太过危险,不适合用于严重食物的治疗,如花生过敏。因此,预防严重食物反应的治疗是一项尚未得到满足的主要需求。我们建议开发和测试花生过敏原(Ara H2)-人Fc(1)嵌合融合蛋白作为用于治疗严重食物过敏的新型过敏原-Fc(1特异性免疫治疗蛋白)的整个平台的原型模型。预计Ara H2-Fc(1)蛋白的治疗指数将显著提高,因为过敏原部分将作为免疫原,诱导标准过敏原免疫治疗的好处,而Fc(1片)则起到阻止任何过敏反应的作用。因此,Ara H2-Fc(1)蛋白将作为免疫原而不是过敏原,从而提供一种安全有效的特定免疫疗法。这种方法的基础是广泛的科学主体,表明人类Fc(RIIb抑制受体)有能力强烈地抑制过敏效应机制。这些关于食物过敏的研究将建立在我们成功开发用于呼吸道过敏的嵌合人类FC(1-CAT过敏原蛋白)的基础上。Tunitas Treateutics,Inc.已与加州大学谈判达成一项独家许可,开发用于治疗食物过敏的嵌合过敏原-Fc(1蛋白质)。目前的提案将为这种治疗方法的商业化道路提供初步步骤,使用花生主要过敏原Ara H2作为模型系统。具体地说,我们将创建所需的基因,在优化的CHO细胞系统中表达Ara H2-Fc(1)融合蛋白,并纯化得到的嵌合蛋白。然后,我们将证明表达的嵌合蛋白保留了变应原IgE和Fc(RIIb结合)的关键特征。最后,我们将证明嵌合蛋白在体外或体内都不能诱导过敏反应。花生特异性嵌合疫苗疗法的批准将是一个机会,为绝大多数花生过敏患者提供安全、有效的免疫治疗疗程。目前一个疗程的免疫治疗费用为1500-2500美元,费用分摊在3-5年期间。由于Ara h-FC(1)蛋白免疫疗法的疗程费用保守地落在类似的范围内,而且预计只有最严重的花生过敏患者最初可能会选择接受免疫疗法,预计几年内美国的年销售额将达到100-300美元。PHS 398/2590(09/04版,2006年4月4日重新发布)页面续格式页面 公共卫生相关性:预防严重食物反应的治疗是一项尚未得到满足的主要医疗需求。花生过敏影响了大约1%的人口,是最严重的食物过敏之一,每年导致3万急诊室就诊,200多人死亡。这项提议的目标是开发一种新的过敏原特异性免疫疗法并将其商业化,以治疗严重的食物过敏。
英文摘要
DESCRIPTION (provided by applicant): The goal of this proposal is to develop and commercialize a novel approach for allergen specific immunotherapy as treatment for severe food allergy. Food allergy affects about 3.5% of the US population and 6% to 8% of young children. It is clearly on the rise. Peanut allergy, which affects around 1% of the population, is among the most severe food allergies, resulting in 30,000 emergency room visits and over 200 deaths per year. Standard allergen protein-based desensitization - immunotherapy as is employed for allergic airways disease - has proven unsuccessful and far too dangerous to use as treatment of severe food, e.g. peanut allergy. Thus treatment to prevent severe food reactions is a major unmet need. We propose to develop and test a peanut allergen (Ara h2)-human Fc(1 chimeric fusion protein as the prototype model for an entire platform of novel allergen-Fc(1 specific immunotherapeutic proteins designed for the treatment of severe food allergy. The Ara h2-Fc(1 protein is predicted to have a marked enhanced therapeutic index as the allergen portion will act as an immunogen to induce the benefits of standard allergen immunotherapy while the Fc(1 piece functions to block any allergic reactions. Thus the Ara h2-Fc(1 protein will act as an immunogen but not an allergen and thereby provide a safe and effective form of specific immunotherapy. Underlying this approach is an extensive body of science showing the ability of human Fc(RIIb inhibitory receptors to acutely inhibit allergic effector mechanisms. These studies on food allergy will build on our success with development of a chimeric human Fc(1-cat allergen protein for respiratory allergy. Tunitas Therapeutics, Inc. has negotiated an exclusive license with the University of California to develop chimeric allergen-Fc(1 proteins for the treatment of food allergy. The current proposal will provide the initial steps on the path to commercialization of this therapeutic approach using Ara h2, the dominant peanut allergen, as a model system. Specifically we will create the required gene, express the Ara h2-Fc(1 fusion protein in an optimized CHO cell system, and purify the resulting chimeric protein. We will then show that the expressed chimeric protein retains the key features of allergen IgE and Fc(RIIb binding. Finally, we will document that the chimeric protein fails to induce allergic reactivity in vitro or in vivo. The approval of a peanut-specific chimeric vaccine therapeutic would be an opportunity to administer a safe, effective course of immunotherapy to the vast majority of peanut-allergic individuals. The current cost of a course of immunotherapy is $1500-2500, with costs spread over a 3-5 year period. With a cost for a treatment course of Ara h-Fc(1 protein immunotherapy conservatively targeted to fall in a similar range and the expectation that only the most severe peanut-allergic individuals may initially choose to receive immunotherapy, annual US sales of $100-300 MM would be expected within several years. PHS 398/2590 (Rev. 09/04, Reissued 4/2006) Page Continuation Format Page PUBLIC HEALTH RELEVANCE: Treatment to prevent severe food reactions is a major unmet medical need. Peanut allergy, which affects around 1% of the population, is among the most severe food allergies, resulting in 30,000 emergency room visits and over 200 deaths per year. The goal of this proposal is to develop and commercialize a novel approach for allergen specific immunotherapy as treatment for severe food allergy.
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A Human Fc Bifunctional Fusion Protein to Treat Severe Allergic Asthma
  • 批准号:
    8057898
  • 项目类别:
  • 资助金额:
    $30.0万
  • 财政年份:
    2011
  • 负责人:
    ANDREW SAXON
  • 依托单位:
A Human Fc Bifunctional Fusion Protein to Treat Severe Allergic Asthma
  • 批准号:
    8249373
  • 项目类别:
  • 资助金额:
    $14.35万
  • 财政年份:
    2011
  • 负责人:
    ANDREW SAXON
  • 依托单位:
A Human Fc Bifunctional Fusion Protein to Treat Severe Allergic Asthma
  • 批准号:
    8523458
  • 项目类别:
  • 资助金额:
    $100.0万
  • 财政年份:
    2011
  • 负责人:
    ANDREW SAXON
  • 依托单位:
A therapeutic Fc gamma Fel d1 chimeric protein vaccine to treat cat allergy
  • 批准号:
    8307102
  • 项目类别:
  • 资助金额:
    $100.0万
  • 财政年份:
    2010
  • 负责人:
    ANDREW SAXON
  • 依托单位:
海外基金