疯牛病在血液中的传播研究。

R Bradley
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摘要

在一项实验发病机制研究中,对患有天然疯牛病的牛进行了全面的组织传染性研究,在该研究中,牛口服感染了来自天然疯牛病病例的牛脑。在牛的疯牛病自然病例中,只在中枢神经系统(大脑、脊髓和视网膜)发现传染性。在骨髓、凝血、灰褐色皮毛、血清或胎牛血清等约50种其他组织中未发现传染性。在发病机制研究中,在感染后35个月(39个月大)首次检测到临床疾病,在血液或任何血液分析成分中未发现感染性。在牛和小鼠的三个独立实验中(i)五个大脑池,(ii)五个脾脏池和(iii)五头牛的淋巴结池进行的实验性肠外刺激是不完整的。然而,尽管大脑已经将疾病传染给了这两个物种(即使在牛中被稀释了大约一百万倍),脾脏池和淋巴结池都没有将疾病传染给任何一个物种,尽管对牛的研究是不完整的。这些实验还表明,牛检测到的传染性每克比小鼠低1000倍左右。在绵羊和山羊的天然痒病、牛的天然疯牛病或牛的实验性疯牛病的血液或任何血液成分中从未检测到传染性。
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BSE transmission studies with particular reference to blood.

Tissue infectivity in BSE has been comprehensively investigated in cattle with natural BSE and during the incubation period in an experimental pathogenesis study in which cattle were challenged orally with infected cattle brain from natural cases. In natural cases of BSE in cattle, infectivity has been found only in the CNS, (the brain, the spinal cord and retina). No infectivity has been found in about 50 other tissues including bone marrow, clotted blood, buffy coat, serum or foetal calf serum. In the pathogenesis study in which clinical disease was first detected at 35 months post-infection (39 months of age), infectivity has not been found in blood or any assayed component of blood. Experimental parenteral challenge of cattle and mice in three separate experiments with (i) a pool of five brains, (ii) a pool of five spleens and (iii) a pool of lymph nodes from five cattle is incomplete. However, whereas the brain has transmitted disease to both species (in cattle even when diluted about one million times) neither the spleen pool nor the lymph node pool has transmitted disease to either, although the cattle study is incomplete. These experiments have also shown that cattle can detect about 1000 times less infectivity/g than can mice. No infectivity has ever been detected in the blood or any component of blood in natural scrapie of sheep and goats, natural BSE of cattle or experimental BSE of cattle.

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Virus removal by filtration. Gamma irradiation of bovine sera. Efficient inactivation of viruses and mycoplasma in animal sera using UVC irradiation. A universal virus inactivant for decontaminating blood and biopharmaceutical products. Serum and serum substitutes: virus safety by inactivation or removal.
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