Pilon John, Loiacono Christina, Okeson Danelle, Lund Sharon, Vercauteren Kurt, Rhyan Jack, Miller Lowell
USDA APHIS WS National Wildlife Research Center, Fort Collins, CO 80521, USA.
Neurosci Lett. 2007 Dec 18;429(2-3):161-4. doi: 10.1016/j.neulet.2007.10.015. Epub 2007 Oct 26.
Chronic wasting disease (CWD) is a transmissible spongiform encephalopathy (TSE) of domestic and wild cervids in North America. To address possible prevention regimens for CWD, we have used a mouse model system and the Rocky Mountain Laboratory (RML) mouse-adapted scrapie prion strain to screen efficacy of potential vaccine candidates. Three peptides derived from the primary amino acid sequence of the prion protein were conjugated to blue carrier protein (BCP) and formulated in an adjuvant containing M. avium subsp. avium. CL57/BL6 mice were vaccinated and boosted with 50 microg of the carrier protein-peptide conjugate formulation; all vaccines produced a humoral immune response as measured by ELISA. Disease challenge with the RML scrapie prion strain revealed anti-prion activity was generated by the vaccine formulations as measured by a delay in clinical disease onset and prolonged survivorship.
慢性消耗病(CWD)是北美家养和野生鹿科动物的一种传染性海绵状脑病(TSE)。为了研究针对CWD可能的预防方案,我们使用了小鼠模型系统和落基山实验室(RML)适应小鼠的羊瘙痒病朊病毒株来筛选潜在疫苗候选物的功效。从朊病毒蛋白的一级氨基酸序列衍生出的三种肽与蓝色载体蛋白(BCP)偶联,并配制在含有鸟分枝杆菌亚种鸟型的佐剂中。用50微克载体蛋白 - 肽偶联物制剂对C57/BL6小鼠进行免疫接种和加强免疫;通过ELISA检测,所有疫苗均产生了体液免疫反应。用RML羊瘙痒病朊病毒株进行疾病攻击显示,通过临床疾病发作延迟和存活期延长来衡量,疫苗制剂产生了抗朊病毒活性。