The S. japonicum-Based pGEX Vector: Commercial Outcomes from Analysis of Model Host-Parasite Relationships in a “North-South” Collaboration

G. Mitchell, K. Davern, Tiu Wu
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Abstract

As judged by widespread utility in protein production from recombinant Escherichia coli and by the magnitude of royalty payments to Melbourne's Walter & Eliza Hall Institute (WEHI), the expression vector pGEX, invented by Dr Donald Smith, has been a significant commercial success. It is based on the 26kDa glutathione S-transferase of Schisto- soma japonicum (Philippines) termed Sj26GST, that emerged from work throughout the 1980's on resistance to infection in a peculiar mouse strain, WEHI 129/J. Sj26GST was the lead vaccine candidate for this human helminth worm being pursued in a long-term collaboration between WEHI in Australia and Dr Edito Garcia's 1 group at the College of Public Health, University of the Philippines in Manila that commenced in 1980. The product, pGEX, is an excellent example of commercial spin-off from basic research in mouse model systems that in- deed evolved into an applied research program but with a very different goal, namely rational molecular vaccine devel- opment.
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基于日本血吸虫的pGEX载体:“南北”合作中模式宿主-寄生虫关系分析的商业成果
从重组大肠杆菌在蛋白质生产中的广泛应用,以及向墨尔本沃尔特与伊丽莎霍尔研究所(WEHI)支付的版税金额来看,唐纳德史密斯博士发明的表达载体pGEX已经取得了重大的商业成功。它是基于日本血吸虫(菲律宾)的26kDa谷胱甘肽s -转移酶,称为Sj26GST,该酶是在整个20世纪80年代对一种特殊小鼠品系WEHI 129/J的感染抗性研究中出现的。Sj26GST是这种人类蠕虫的主要候选疫苗,这是澳大利亚WEHI与马尼拉菲律宾大学公共卫生学院Edito Garcia博士小组于1980年开始的长期合作。该产品pGEX是小鼠模型系统基础研究的商业衍生品的一个极好例子,它确实演变成一个应用研究项目,但目标非常不同,即合理的分子疫苗开发。
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