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An in vitro assay system as a potential replacement for the histamine sensitisation test for acellular pertussis based combination vaccines

机译:一种体外测定系统,可以替代基于脱细胞百日咳的组合疫苗的组胺敏化试验

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摘要

The histamine sensitisation test (HIST) for pertussis toxin is currently an official batch release test for acellular pertussis containing combination vaccines in Europe and North America. However, HIST, being a lethal endpoint assay, often leads to repeated tests due to large variations in test performance. Although a more precise HIST test based on measurement of temperature reduction after the histamine challenge is used in Asian countries, this test still uses animals. An in vitro test system based on a combination of enzyme coupled-HPLC and carbohydrate-binding assays with results analysed by a mathematical formula showed a good agreement with the in vivo HIST results based on measurement of temperature reduction after histamine challenge. The new in vitro test system was shown to be a potential alternative to the current in vivo HIST.
机译:百日咳毒素的组胺敏化试验(HIST)目前是欧洲和北美针对脱细胞百日咳的正式批量释放试验,其中包含联合疫苗。但是,HIST是一种致命的终点检测方法,由于测试性能的巨大差异,通常会导致重复测试。尽管在亚洲国家/地区使用了基于组胺激发后降温测量的更精确的HIST测试,但该测试仍使用动物。基于酶联HPLC和碳水化合物结合测定相结合的体外测试系统,并通过数学公式进行分析,结果与基于组胺激发后温度降低的体内HIST结果具有很好的一致性。新的体外测试系统被证明是当前体内HIST的潜在替代品。

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