Effects of initiation of 3'-azido,3'-deoxythymidine (zidovudine) treatment at different times after infection of rhesus monkeys with simian immunodeficiency virus.

Effects of initiation of 3'-azido,3'-deoxythymidine (zidovudine) treatment at different times after infection of rhesus monkeys with simian immunodeficiency virus.
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恒河猴感染猿猴免疫缺陷病毒后不同时间开始3-叠氮,3-脱氧胸苷(齐多夫定)治疗的效果。

DOI:
10.1093/infdis/168.4.825
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发表时间:
1993
期刊:
The Journal of infectious diseases
影响因子:
--
通讯作者:
Baskin,GB
Baskin,GB
中科院分区:
--
文献类型:
--
作者:
Martin,LN;Murphey-Corb,M;Soike,KF;Davison-Fairburn,B;Baskin,GB

文献摘要

被引文献

相似文献

本文观察了恒河猴接种猴免疫缺陷病毒(SIV)后不同时间用齐多夫定(ZIDO)开始治疗的效果。在静脉内接种10 ID 50的SIV后1、8、24或72 h,开始100 mg/kg/天(25 mg/kg,皮下注射,每6 h一次)的齐多夫定治疗。处理持续28天,并将结果与盐水处理的对照组进行比较。接种后14天(AI)的血清感染性病毒滴度显着下降后,治疗开始1,8,或24小时AI。滴度与治疗开始时间相关。1-72小时AI开始的治疗可防止持续性SIV抗原血症的建立;早期开始治疗观察到更大的效果。治疗开始1-8小时AI导致病毒抗原血症水平下降14天AI和延迟的CD 4 + CD 29+血淋巴细胞减少。较早开始治疗导致抗原血症复发延迟,生存期延长。在已知暴露的情况下,早期开始治疗对于限制初始病毒复制和传播可能很重要。
The effects of initiating treatment with 3′-azido-3′-deoxythymidine (zidovudine) at different times after inoculation of simian immunodeficiency virus (SIV) were investigated in rhesus monkeys. Zidovudine treatments of 100 mg/kg/day (25 mg/kg, subcutaneously every 6 h) were initiated 1, 8, 24, or 72 h after intravenous inoculation of 10 ID50ofSIV. Treatments continued for 28 days, and results were compared with those of saline-treated controls. Serum infectious virus titers 14 days after inoculation (AI) significantly decreased after treatment initiation 1, 8, or 24 h AI. Titers were correlated with the time treatment was initiated. Treatments initiated 1–72 h AI prevented the establishment of persistent SIV antigenemia; greater effects were observed with earlier initiation of treatment. Treatments initiated 1–8 h AI resulted in decreased levels of viral antigenemia 14 days AI and delayed decreases in CD4+CD29+blood lymphocytes. Earlier treatment initiation resulted in delayed recurrence of antigenemia, with a tendency for longer survival. Early initiation of treatment may be important for limiting initial viral replication and dissemination in cases of known exposure.