Rickard M D, Harrison G B, Heath D D, Lightowlers M W
CSIRO Division of Animal Health, Parkville, Victoria, Australia.
Parasitology. 1995;110 Suppl:S5-9. doi: 10.1017/s0031182000001438.
Several years have elapsed since the publication by Johnson et al. (1989) of the cloning of a recombinant antigen from the cestode parasite Taenia ovis which stimulated high levels of protective immunity in sheep. A great deal of subsequent research and development was necessary to bring the fledgling vaccine to the point of being a registered commercial product. The results of these subsequent studies are dealt with briefly in this paper, including the results of field trials. The T. ovis vaccine was registered by the New Zealand Animal Remedies Board in February 1994. Where then is the commercial product? This paper gives a background to market problems which have emerged through the politics (and realities) of the NZ T. ovis control campaign. It serves as notice that the best science dedicated to producing vaccines or products for parasitic, or other, diseases often faces significant hurdles in the real world of commerce and politics.
自约翰逊等人(1989年)发表从绦虫寄生虫绵羊带绦虫克隆重组抗原的文章以来,已经过去了数年。该重组抗原能刺激绵羊产生高水平的保护性免疫。为了使这个初出茅庐的疫苗成为注册的商业产品,还需要进行大量后续的研究和开发工作。本文简要介绍了这些后续研究的结果,包括田间试验的结果。绵羊带绦虫疫苗于1994年2月由新西兰动物药品委员会注册。那么该商业产品在哪里呢?本文介绍了由于新西兰绵羊带绦虫防控运动的政治因素(以及现实情况)而出现的市场问题背景。它提醒人们,致力于生产针对寄生虫病或其他疾病的疫苗或产品的最佳科学成果,在商业和政治的现实世界中往往面临重大障碍。