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Adjuvants: present regulatory challenges

机译:佐剂:目前的监管挑战

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Research on new adjuvants and delivery systems has expanded dramatically in the last decade. New generation vaccines, based on recombinant proteins, synthetics, and conjugated antigens have emerged but they have limitations because of their poor immunogenic properties, and therefore more cooperative adjuvants for the promotion of the immune response are required. Different molecules have been screened for their ability to enhance the immune response to vaccine antigens, e.g. liposomes, protein cochleate formulations, ISCOMs and cytokines, to name the few. However, most of the vaccines that are currently licensed use aluminum salts or calcium phosphate.
机译:在过去的十年中,对新佐剂和给药系统的研究已大大扩展。已经出现了基于重组蛋白,合成蛋白和结合抗原的新一代疫苗,但是由于它们的免疫原性差而受到限制,因此需要更多的协同佐剂来促进免疫反应。已经筛选出不同的分子增强针对疫苗抗原的免疫应答的能力,例如针对抗原。脂质体,蛋白质耳蜗制剂,ISCOM和细胞因子,仅举几例。但是,当前获得许可的大多数疫苗都使用铝盐或磷酸钙。

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