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DESCRIPTION (provided by applicant): Food allergy, an aberration of oral tolerance, occurs in 6% of children and 3.5% of adults in the United States. Peanut allergy is one of the most common food allergies; most children develop this allergy early in life, do not outgrow it and are at risk for severe and life-ending anaphylactic reactions. Currently there is not a proactive treatment for peanut allergy but we along with others are developing specific types of immunotherapy that will cause these patients to be no longer allergic to peanuts. The significance of this proposal is based on our landmark studies that have examined the effects of peanut oral immunotherapy (OIT) showing a substantial increase in the amount of peanut that a peanut allergic patient can ingest while on therapy (desensitization) and in some cases causing long-term clinical tolerance when the therapy is discontinued. We have identified initial changes in basophil/mast cell reactivity, antigen-specific T cell responses and systemic humoral immune responses in these subjects. Our hypothesis is that peanut OIT will alter the early signaling pathways of basophils/mast cells causing clinical desensitization and then clinical tolerance will develop because of the interrelated changes in allergen-specific T- and B-cells. The long-term goal of this proposal is to better understand the mechanism of the development of oral tolerance to foods in young children treated with allergen immunotherapy. To accomplish this goal our specific aims are the following: Aim 1: Determine the mechanism(s) by which OIT induces hyporesponsiveness in basophils/mast cells in peanut allergic subjects on peanut OIT, Aim 2: Determine the peanut allergen-specific CD4+ T cell frequencies and phenotypes, as well as the suppressive function of Treg cells, that are associated with the development of clinical tolerance to peanuts, Aim 3: Determine the effect of peanut-specific mucosal and systemic humoral immune responses in OIT on clinical tolerance. The studies will help us identify the mechanism and durability of the desensitized state and then the development of tolerance to foods after OIT. A treatment for peanut allergy is critically needed, the completion of these studies will provide a strong scientific basis for the development of OIT and other types of therapy that hope to produce long-term clinical tolerance to peanuts and other foods.
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Tree nut- and sesame-specific IgE do not decrease from baseline with peanut oral immunotherapy (OIT).
花生口服免疫疗法 (OIT) 不会使坚果和芝麻特异性 IgE 较基线下降。
DOI: 10.1016/j.anai.2012.09.004
发表时间: 2012
期刊: Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology
影响因子: --
作者: [Bird,JAndrew, Kulis,Michael, Burk,CaitlinM, Vickery,BrianP, Jones,StacieM, Burks,Wesley]
通讯作者: Burks,Wesley
DOI: 10.1016/j.jaci.2016.07.030
发表时间: 2017-03
期刊: The Journal of allergy and clinical immunology
影响因子: --
作者: [Virkud YV, Burks AW, Steele PH, Edwards LJ, Berglund JP, Jones SM, Scurlock AM, Perry TT, Pesek RD, Vickery BP]
通讯作者: Vickery BP
DOI: 10.1172/jci87492
发表时间: 2016-11-01
期刊: The Journal of clinical investigation
影响因子: --
作者: [Ang WX, Church AM, Kulis M, Choi HW, Burks AW, Abraham SN]
通讯作者: Abraham SN
NEW HORIZONS IN THE PREVENTION AND TREATMENT OF FOOD ALLERGY
  • 批准号:
    9443585
  • 项目类别:
  • 资助金额:
    $585.47万
  • 财政年份:
    2017
  • 负责人:
    A. Wesley Burks
  • 依托单位:
NEW HORIZONS IN THE PREVENTION AND TREATMENT OF FOOD ALLERGY
  • 批准号:
    9889023
  • 项目类别:
  • 资助金额:
    $585.5万
  • 财政年份:
    2017
  • 负责人:
    A. Wesley Burks
  • 依托单位:
NEW HORIZONS IN THE PREVENTION AND TREATMENT OF FOOD ALLERGY
  • 批准号:
    10581628
  • 项目类别:
  • 资助金额:
    $1349.33万
  • 财政年份:
    2017
  • 负责人:
    A. Wesley Burks
  • 依托单位:
NEW HORIZONS IN THE PREVENTION AND TREATMENT OF FOOD ALLERGY
  • 批准号:
    10631369
  • 项目类别:
  • 资助金额:
    $299.87万
  • 财政年份:
    2017
  • 负责人:
    A. Wesley Burks
  • 依托单位:
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