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Formulation of botulinum neurotoxin heavy chain fragments for vaccine development: mechanisms of adsorption to an aluminum-containing adjuvant

机译:用于疫苗开发的肉毒杆菌神经毒素重链片段的配制:吸附至含铝佐剂的机制

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Heavy chain fragments of botulinum neurotoxin serotypes A and B are being developed as a bivalent vaccine for botulism. To potentiate the immune response, an aluminum containing adjuvant will be formulated with the two antigens. The adsorption mechanisms of each antigen to aluminum phosphate and aluminum hydroxide adjuvants were studied. The adsorption of the serotype A antigen to each adjuvant, and the serotype B antigen to aluminum phosphate adjuvant, is dependent on electrostatic attractive forces. The serotype A antigen is basic, and pretreatment with phosphate anions is required for favorable adsorption conditions to aluminum hydroxide adjuvant. In contrast, the serotype B antigen displays a high affinity to aluminum hydroxide adjuvant even when the two species possess the same charge. It is proposed that the serotype B antigen is adsorbed to aluminum hydroxide adjuvant by a ligand exchange mechanism.
机译:肉毒杆菌神经毒素血清型A和B的重链片段正在开发为肉毒中毒的二价疫苗。为了增强免疫应答,将用两种抗原配制含铝佐剂。研究了每种抗原对磷酸铝和氢氧化铝佐剂的吸附机理。血清型A抗原对每种佐剂的吸附以及血清型B抗原对磷酸铝佐剂的吸附取决于静电吸引力。血清型A抗原是碱性的,为使氢氧化铝佐剂具有良好的吸附条件,需要用磷酸根阴离子进行预处理。相反,即使两个物种具有相同的电荷,血清型B抗原对氢氧化铝佐剂也显示出高亲和力。提出通过配体交换机制将血清型B抗原吸附到氢氧化铝佐剂上。

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