建立含血浆源性乙型肝炎表面抗原的乙型肝炎疫苗国际参比试剂的合作研究

Morag Ferguson , Valerie Seagroatt , Geoffrey C. Schild
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引用次数: 2

摘要

为建立一种适用于乙型肝炎疫苗免疫原性测定的国际标准试剂,开展了一项合作研究。为拟议的国际参考试剂和其他三种血浆源性乙型肝炎疫苗确定了在50%的试验动物中诱导抗体所需的极限稀释度。这些制剂的最低抗原剂量在各实验室之间差别很大(相差100倍)。然而,相对于提议的国际参考试剂,疫苗效力的表达将实验室之间的差异减少到10倍范围内。参考试剂用于乙型肝炎疫苗在小鼠(或豚鼠)免疫原性研究中的测定。对于不同工艺生产的产品,需要进行人体临床试验,以确定动物和人类免疫原性效力之间的相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A collaborative study to establish the international reference reagent for hepatitis B vaccine containing plasma-derived hepatitis B surface antigen

A collaborative study was conducted to establish a suitable international reference reagent for hepatitis B vaccine for use in immunogenicity assays. The limiting dilution required to induce antibodies in 50% of the test animals was determined for the proposed international reference reagent and three other plasma-derived hepatitis B vaccines. The minimum antigenic dose of these preparations varied widely (100-fold range) between laboratories. However, the expression of potencies of vaccines relative to the proposed International Reference Reagent reduced the variation between laboratories to within a 10-fold range. The reference reagent is intended for use in assays of hepatitis B vaccines in mouse (or guinea-pig) immunogenicity studies. For products made by different procedures, clinical trials in humans are necessary to establish a correlation between the immunogenic potency in animals and man.

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