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In vitro activation of antigen-presenting cells (APC) by defined composition of Quillaja saponaria Molina triterpenoids

机译:定义的皂树莫利纳三萜类化合物在体外激活抗原呈递细胞(APC)

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摘要

The capacity of adjuvants to stimulate cytokine production by APC is important for the initiation of the immune response. Novel adjuvant formulations based on the iscom technology have been developed using selected triterpenoid components from Quillaja saponaria Molina. Five of these new Quillaja formulations were used to prepare matrix (an antigen-free particle) and tested for their capacity to stimulate IL-1 secretion by murine peritoneal cells in vitro. The formulation denominated QH 7.0.3 was superior to the other matrix formulations, including the original spikoside matrix. The QH 7.0.3 formulation in iscoms containing influenza virus envelope antigens induced IL-1 secretion more efficiently than the antigen-free matrix, or a mixture of matrix and viral antigens, or the free Quillaja components of similar composition. Compared with adjuvants known as IL-1 inducers, QH 7.0.3 flu-iscoms were as efficient as the most prominent IL-1 inducer, i.e. lipopolysaccaride (LPS) and superior to cholera toxin (CT) and muramyl dipeptide (MDP). These results indicate that the composition per se of triterpenoids included in iscoms or matrix has a prominent influence on the level of APC activation which may result in qualitatively different immune responses in vivo
机译:佐剂刺激APC产生细胞因子的能力对于免疫应答的启动很重要。已经使用选自Quillaja saponaria Molina的三萜类成分开发了基于iscom技术的新型佐剂。这些新的Quillaja制剂中的五种用于制备基质(无抗原颗粒),并测试了它们体外刺激鼠腹膜细胞刺激IL-1分泌的能力。命名为QH 7.0.3的配方优于其他基质配方,包括原始的spikoside基质。含有流感病毒包膜抗原的iscoms中的QH 7.0.3制剂比无抗原的基质,基质和病毒抗原的混合物,或类似组成的游离Quillaja组分更有效地诱导IL-1分泌。与被称为IL-1诱导剂的佐剂相比,QH 7.0.3 flu-iscoms与最著名的IL-1诱导剂即脂多糖(LPS)一样有效,并且优于霍乱毒素(CT)和鼠李二肽(MDP)。这些结果表明,iscoms或基质中包含的三萜类化合物本身的组成对APC激活水平有显着影响,这可能导致体内免疫反应发生质的不同

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