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用无环核苷膦酸类似物9-(2-膦酰甲氧基乙基)腺嘌呤(PMEA)治疗羔羊的维斯纳病毒感染。

Treatment of visna virus infection in lambs with the acyclic nucleoside phosphonate analogue 9-(2-phosphonylmethoxyethyl)adenine (PMEA).

作者信息

Thormar H, Georgsson G, Gunnarsson E, Naesens L, Torsteinsdóttir S, Balzarini J, De Clercq E

机构信息

Institute of Biology, University of Iceland, Reykjavik, Iceland.

出版信息

Antivir Chem Chemother. 1998 May;9(3):245-52. doi: 10.1177/095632029800900305.

Abstract

Nucleoside and nucleotide analogues, which are inhibitors of human immunodeficiency virus reverse transcriptase, are highly active inhibitors of visna virus replication in cell cultures. One such analogue, the acyclic nucleoside phosphonate PMEA, has also been found to have a prophylactic effect on visna virus infection in lambs. In the present study, lambs were injected subcutaneously with 10 mg/kg PMEA three times a week starting 4 weeks after inoculation with visna virus, when brain infection had been established. After 3 weeks of treatment there was a reduction in the amount of virus isolated from blood cells of PMEA-treated lambs compared to controls and during the remaining 7 months of drug treatment there was significantly less virus isolated from the blood cells of treated lambs than of controls. Antibody response against visna virus was also slower in the treated than in the untreated control group. On the other hand, there was no difference in the amount of virus isolated from various organs of the two groups and the severity of CNS lesions in sheep treated with PMEA for 8 months was comparable to that found in untreated controls, even though PMEA reached concentrations in the cerebrospinal fluid which were well in excess of the EC50 value of the drug for visna virus.

摘要

核苷和核苷酸类似物是人类免疫缺陷病毒逆转录酶的抑制剂,在细胞培养中是维斯纳病毒复制的高效抑制剂。一种这样的类似物,无环核苷膦酸PMEA,也已被发现对羔羊的维斯纳病毒感染有预防作用。在本研究中,从接种维斯纳病毒4周后开始,当脑感染已经确立时,给羔羊每周皮下注射3次10mg/kg的PMEA。治疗3周后,与对照组相比,从接受PMEA治疗的羔羊血细胞中分离出的病毒量有所减少,并且在药物治疗的剩余7个月期间,从治疗羔羊的血细胞中分离出的病毒明显少于对照组。治疗组对维斯纳病毒的抗体反应也比未治疗的对照组慢。另一方面,两组从各个器官分离出的病毒量没有差异,并且用PMEA治疗8个月的绵羊中枢神经系统病变的严重程度与未治疗的对照组相当,尽管PMEA在脑脊液中的浓度远远超过该药物对维斯纳病毒的EC50值。

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