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含乙肝病毒和非甲非乙肝炎病毒的血液成分的光化学去污处理

Photochemical decontamination of blood components containing hepatitis B and non-A, non-B virus.

作者信息

Alter H J, Creagan R P, Morel P A, Wiesehahn G P, Dorman B P, Corash L, Smith G C, Popper H, Eichberg J W

机构信息

Department of Transfusion Medicine, Warren Grant Magnuson Clinical Center, National Institutes of Health Bethesda, MD 20205.

出版信息

Lancet. 1988;2(8626-8627):1446-50. doi: 10.1016/s0140-6736(88)90931-2.

Abstract

Diluted plasma samples containing 10(2), 10(3), 10(4), and 10(5) chimpanzee infectious doses (CID) of a human non-A, non-B hepatitis virus (NANBV) were treated with a combination of two psoralen compounds, 4'-aminomethyl-4,5',8-trimethylpsoralen and 4,5',8-trimethylpsoralen, and exposed to long wavelength ultraviolet. Each dilution was then transfused into one of four chimpanzees. In a second experiment, three samples containing 10(4.5) CID of hepatitis B virus (HBV) and two samples containing 10(4) CID of NANBV were treated with 8-methoxypsoralen (8-MOP) and ultraviolet irradiation. Two chimpanzees were each transfused with both a treated HBV and a treated NANBV sample. The third chimpanzee was inoculated with a treated HBV sample alone. In the six months after inoculation none of the animals showed biochemical or histological evidence of hepatitis. In experiments involving NANBV inocula, the susceptibility of the animals was confirmed by subsequent challenge with untreated NANBV. Factor VIII concentrate containing virus and photochemically treated as in the first experiment retained an average of 91% of its activity while that in the second experiment retained 94% of its activity.

摘要

含有10²、10³、10⁴和10⁵个黑猩猩感染剂量(CID)的一种人类非甲非乙型肝炎病毒(NANBV)的稀释血浆样本,用两种补骨脂素化合物(4'-氨甲基-4,5',8-三甲基补骨脂素和4,5',8-三甲基补骨脂素)的组合进行处理,并暴露于长波长紫外线。然后将每种稀释液分别输注到四只黑猩猩中的一只体内。在第二个实验中,三个含有10⁴·⁵个CID的乙型肝炎病毒(HBV)样本和两个含有10⁴个CID的NANBV样本用8-甲氧基补骨脂素(8-MOP)和紫外线照射进行处理。两只黑猩猩分别输注了经处理的HBV样本和经处理的NANBV样本。第三只黑猩猩仅接种了经处理的HBV样本。在接种后的六个月内,没有一只动物表现出肝炎的生化或组织学证据。在涉及NANBV接种物的实验中,通过随后用未处理的NANBV进行攻击来确认动物的易感性。含有病毒并如第一个实验那样进行光化学处理的因子VIII浓缩物平均保留了其91%的活性,而在第二个实验中保留了94%的活性。

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