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Immune focusing to major allergens prevents the recognition of minor antigens and allergy formation

机译:对主要过敏原的免疫焦点可防止识别次要抗原和过敏的形成

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Natural allergens are complex mixtures of multiple proteins,polysaccharides,and glycoproteins.They do not replicate inside the body and thus the concentration of individual proteins contacting immune system is very low.On the contrary,pathogens arc able to replicate after invasion by this mean increasing significantly the local concentration of antigens originated from these pathogens.Antigen presenting cells(APC)process foreign antigens originated from extracellular pathogens as well as from allergens through endosomai compartment where antigenic peptides are loaded on MHC class 11 molecules.The number of MHC complexes carrying the antigenic peptides on the surface of APC is proportional to the antigen concentration in endosomes.The selection of T cells recognizing different proteins from pathogens results both from the competition for MHC-peptide complexes and the number of APC-T cell contacts.Thus,immune response to pathogens is focused to dominant antigens whose peptides presented in excess,while allergic response is probably not focused due to the low concentration of allergen proteins in APC.The aim of this work was i)to estimate the number of proteins recognized during immunization with polycomponent allergen extract and ii)whether it is possible to focus allergic response to a single major allergen
机译:天然过敏原是多种蛋白质,多糖和糖蛋白的复杂混合物。他们在身体内部没有复制,因此接触免疫系统的个体蛋白质的浓度非常低。相反,病原体能够在这种平均增加后进行侵袭后复制显着显着地,源于这些病原体的抗原局部浓度。呈细胞(APC)过程源自细胞外病原体以及通过胚乳肽的过敏原,其中抗原肽在MHC级别11分子上。携带的MHC复合物的数量APC表面上的抗原肽与底体中的抗原浓度成比例。识别来自病原体的不同蛋白质的T细胞的选择结果来自MHC-肽复合物的竞争和APC-T细胞接触的数量。属,免疫应答对病原体的重点是肽呈现的主要抗原过量,而过敏反应可能由于APC中的过敏原蛋白质浓度低而不是聚焦。这项工作的目的是i)估计在用多剂量过敏原提取物和II的免疫接种期间识别的蛋白质数量是可能的对整个主要过敏原的过敏反应

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