O'Rourke K I, Baszler T V, Besser T E, Miller J M, Cutlip R C, Wells G A, Ryder S J, Parish S M, Hamir A N, Cockett N E, Jenny A, Knowles D P
Animal Disease Research Unit, Animal Research Service, U.S. Department of Agriculture, College of Veterinary Medicine, Washington State University, Pullman 99164-6630, USA.
J Clin Microbiol. 2000 Sep;38(9):3254-9. doi: 10.1128/JCM.38.9.3254-3259.2000.
Ovine scrapie is a member of the transmissible spongiform encephalopathies (TSEs), a heterogeneous family of fatal neurologic disorders characterized by deposition of an abnormal isoform (prion protein [PrP] PrP-Sc) of a cellular sialoglycoprotein in neural tissue. PrP-Sc is detectable in some lymphoid tissues of infected sheep months or years before development of clinical disease. Detection of PrP-Sc in these tissues is the basis for live-animal testing. In this study, we characterize the performance of a preclinical diagnostic test for ovine scrapie based on a monoclonal antibody (MAb)-based immunohistochemistry assay of nictitating membrane ("third eyelid")-associated lymphoid tissue. The results of third eyelid immunohistochemistry assay agreed with the scrapie status of the sheep for 41 of 42 clinical suspects with confirmed scrapie and 174 of 175 sheep without scrapie. Third eyelid sampling agreed with the scrapie status for 36 of 41 clinically normal sheep positive for PrP-Sc immunostaining of brain tissue, including 27 sheep with positive biopsy specimens that progressed to clinical disease with confirmed scrapie 3 to 20 months after biopsy. The assay used MAb F89/160.1.5, which binds to residues 142 to 145 of ovine PrP. This antibody can be used in combination with MAb F99/97. 6.1, which binds to residues 220 to 225. One or both MAbs in this cocktail recognize PrP sequences conserved in most mammalian species in which natural TSEs have been reported. Immunohistochemistry assay of routinely formalin-fixed lymphoid tissues with a cocktail of pan-specific MAbs is a practical, readily standardized live-animal and preclinical test for ovine scrapie.
绵羊瘙痒病是传染性海绵状脑病(TSEs)的一种,TSEs是一类异质性的致命神经疾病,其特征是一种细胞唾液酸糖蛋白的异常异构体(朊病毒蛋白[PrP] PrP-Sc)在神经组织中沉积。在临床疾病出现前数月或数年,可在受感染绵羊的一些淋巴组织中检测到PrP-Sc。在这些组织中检测PrP-Sc是活体动物检测的基础。在本研究中,我们基于对瞬膜(“第三眼睑”)相关淋巴组织的单克隆抗体(MAb)免疫组织化学分析,对绵羊瘙痒病临床前诊断试验的性能进行了表征。瞬膜免疫组织化学分析结果与42只临床疑似确诊瘙痒病绵羊中的41只以及175只无瘙痒病绵羊中的174只的瘙痒病状态一致。对于41只脑组织PrP-Sc免疫染色呈阳性的临床正常绵羊,瞬膜采样结果与瘙痒病状态一致,其中27只绵羊活检标本呈阳性,在活检后3至20个月发展为确诊瘙痒病的临床疾病。该试验使用了MAb F89/160.1.5,它与绵羊PrP的142至145位残基结合。这种抗体可与结合220至225位残基的MAb F99/97.6.1联合使用。该混合物中的一种或两种MAb识别在已报道自然TSEs的大多数哺乳动物物种中保守的PrP序列。用泛特异性MAb混合物对常规福尔马林固定的淋巴组织进行免疫组织化学分析,是一种用于绵羊瘙痒病的实用、易于标准化的活体动物和临床前检测方法。