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New product development with the innovative biomolecular sublingual immunotherapy formulations for the management of allergic rhinitis

机译:利用创新的生物分子舌下免疫疗法配方开发新产品用于治疗过敏性鼻炎

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摘要

The molecular allergy technique, currently defined as component-resolved diagnosis, significantly improved the diagnosis of allergy, allowing for differentiation between molecules actually responsible for clinical symptoms (genuine sensitizers) and those simply cross-reacting or shared by several sources (panallergens), thus influencing the appropriate management of a patient’s allergy. This also concerns allergen immunotherapy (AIT), which may be prescribed more precisely based on the component-resolved diagnosis results. However, the advance in diagnosis needs to be mirrored in AIT. According to consensus documents and to expectations of specialists, therapy should be based on standardized extracts containing measured amounts of the clinically relevant molecules, ie, the major allergens. The new generation of extracts for sublingual immunotherapy fulfills these requirements and are thus defined as biomolecular (BM). BM refers to natural extracts with a defined content of major allergens in micrograms. All Staloral BM products are indicated for the treatment of allergic rhinitis with or without asthma. The effectiveness of AIT is related to its ability to modify the immunological response of allergic subjects. The 5-grass and house dust mite extracts were evaluated addressing the T helper 1, T helper 2, and T helper 3 cells by polymerase chain reaction array on mRNA extracted from Waldeyer’s ring tissue (adenoids). Sublingual immunotherapy with a defined content of major allergens in micrograms induced a strong downregulation of genes involved in T helper 2 and T helper 1 activation and function, allowing the definition of the immunologic effect as “bio-homeostatic”. This clinical and immunological model must be implemented with respect to other allergens, thus expanding the application of a treatment with a unique disease-modifying capacity.
机译:分子过敏技术(目前定义为成分分辨诊断)显着改善了过敏的诊断,可以区分实际上负责临床症状的分子(真正的敏化剂)和那些简单地交叉反应或由多个来源共享的分子(全变应原),因此影响对患者过敏的适当管理。这也涉及变应原免疫疗法(AIT),可根据组分分辨的诊断结果更精确地开出处方。但是,诊断的进展需要在AIT中反映出来。根据共识文件和专家的期望,治疗应基于标准化提取物,该提取物含有一定量的临床相关分子,即主要过敏原。用于舌下免疫治疗的新一代提取物满足了这些要求,因此被定义为生物分子(BM)。 BM是指具有确定的主要过敏原含量(以微克为单位)的天然提取物。所有Staloral BM产品均适用于治疗有或没有哮喘的过敏性鼻炎。 AIT的有效性与其改变过敏性受试者免疫应答的能力有关。通过从Waldeyer环组织(腺样体)提取的mRNA的聚合酶链反应阵列,评估了5种草和家中尘螨提取物对T辅助细胞1,T辅助细胞2和T辅助细胞3细胞的作用。舌下免疫疗法中,主要过敏原的含量定义为微克,导致T辅助2和T辅助1激活和功能相关基因的强烈下调,从而将免疫学作用定义为“生物体内平衡”。必须针对其他变应原实施该临床和免疫模型,从而扩大具有独特疾病缓解能力的治疗方法的应用。

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