肽
接种疫苗
抗原
促性腺激素释放激素
阉割
生物
免疫
医学
内分泌学
内科学
免疫学
激素
生物化学
促黄体激素
作者
Rob H. Meloen,J.A. Turkstra,H. Lankhof,Wouter C. Puijk,W.M.M. Schaaper,G. Dijkstra,C. J. G. Wensing,Ria B. Oonk
出处
期刊:Vaccine
[Elsevier BV]
日期:1994-01-01
卷期号:12 (8): 741-746
被引量:102
标识
DOI:10.1016/0264-410x(94)90226-7
摘要
Active immunization to immunomodulate regulatory processes suffers from the disadvantage that the antigen is usually ‘self’ and therefore poorly immunogenic. This has been well illustrated by the long-standing experience with immunocastration vaccines targeting GnRH, a ten amino acid peptide. Not all animals vaccinated with these vaccines are equally affected, even after multiple vaccinations. This is a severe handicap when immunocastration vaccines are applied to male piglets to circumvent surgical castration. Surgical castration is universally practised to prevent boar taint, produced in the testicles of mature boars. Alternative immunocastration is only acceptable if all animals are equally affected using a minimum of vaccinations. Vaccines based on the GnRH peptide itself cannot meet these goals. We showed that using a GnRH-like peptide, a 20 amino acid tandem repeat of the amino acid sequence of the GnRH peptide, these goals can be attained. Using the tandem GnRH peptide to vaccinate male piglets completely abolished the development and endocrinological functioning of the testicles, in contrast to monomer GnRH. These results show that superior antigens can be made for effective immunomodulation by appropriate alteration of the antigen.
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