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Sublingual immunotherapy in spray a new way of dispensing allergy vaccins

机译:喷洒一种新的分配过敏疫苗的舌下免疫疗法

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Immunotherapy is the only allergy treatment directed to the cause of the disease. Immunotherapy is used for more than 100 years empirically for a long time, but its effect is now explained by molecular biology (1, 2, 10, 12, 13).The end points for immunotherapy are the relief of symptoms, improvement of quality of life and "in vivo" and "in vitro" evidence of benefits.Nowadays is generally agreed that allergen immunotherapy is the only treatment that can modify the immune response to allergen and alter the cause of allergic disease (1, 2, 10, 13). Proposed mechanisms of immunotherapy are a early desensitization of basophils a decrease of specific IgE, increase on IgG antibodies the "old" blocking antibodies a shift from TH2 to TH1 cells, activation of Treg cells with production of IL-10 and TGF Beta and a decrease of inflammatory molecules and cellules with T-cell anergy (1, 2, 11, 14). During the immune response to immunotherapy allergen can be taken up by dendritic cells namely in buccal mucosal and the allergen be presented to T-cells in presence of IL-12 causing a TH1 shift with activation of TReg CD4+CD25 cells releasing IL-10 and blocking TH2 response leading to decreased recruitment of pro-inflammatory cells. An increase of IL-10 after immunotherapy has been clearly shown in the last few years (1, 10).
机译:免疫疗法是针对疾病原因的唯一过敏治疗。免疫疗法长期使用超过100年,但现在其效果现在由分子生物学(1,2,10,12,13)解释。免疫疗法的终点是症状的缓解,提高质量生命和“体内”和“体外”益处的证据。目前一致认为过敏原免疫疗法是唯一可以改变过敏原的免疫反应和改变过敏性疾病原因的唯一治疗方法(1,2,10,13) 。提出的免疫疗法机制是嗜碱性粒细胞的早期脱敏特异性IgE的降低,IgG抗体的增加“旧”阻断抗体从TH2到Th1细胞的转变,通过产生IL-10和TGFβ的Treg细胞的激活和降低炎症分子与T细胞毒剂(1,2,11,14)的炎症分子和纤维素。在对免疫疗法的免疫反应期间,可以在颊粘膜中占用树突粘膜,并且在IL-12存在下呈现给T细胞的过敏原,导致Th1转变为释放IL-10的Treg CD4 + CD25细胞。阻断TH2响应导致降低促炎细胞的募集。在过去几年(1,10)中明确显示免疫疗法后IL-10的增加。

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