Klein R J, Friedman-Kien A E, Brady E
Antimicrob Agents Chemother. 1974 Apr;5(4):409-12. doi: 10.1128/AAC.5.4.409.
The antiviral efficacy of 9-beta-d-arabinofuranosyladenine (ara-A) was evaluated in localized lesions produced by the intradermal inoculation of rabbits with vaccinia virus (VV) and rabbit Shope fibroma virus (SFV). Ara-A administered intraperitoneally suppressed or significantly reduced the cutaneous pustular lesions produced by VV as well as the benign skin tumors caused by the SFV. With a daily dose of 300 mg/kg given for 5 days starting at the time of infection, or with 600 mg/kg daily starting 3 days after inoculation, we were able to suppress completely the formation of tumors induced by the SFV. The appearance of pustular lesions induced by VV was completely suppressed by a dose of 600 mg of ara-A per kg given for 3 days when the treatment was initiated at the time of infection, but a significant reduction in the number of pustular lesions was obtained with a single dose of 600 mg/kg, or with five doses of 300 mg/kg starting 24 h after inoculation. No toxic effect of ara-A was noted in the treated rabbits.
通过给家兔皮内接种痘苗病毒(VV)和兔肖普纤维瘤病毒(SFV)产生局部损伤,评估了9-β-D-阿拉伯呋喃糖基腺嘌呤(ara-A)的抗病毒效果。腹腔注射ara-A可抑制或显著减少由VV产生的皮肤脓疱损伤以及由SFV引起的良性皮肤肿瘤。从感染时开始,每日剂量为300mg/kg,连续给药5天,或者从接种后3天开始,每日剂量为600mg/kg,我们能够完全抑制由SFV诱导的肿瘤形成。当在感染时开始治疗,给予每千克600mg ara-A,连续给药3天,可完全抑制由VV诱导的脓疱损伤的出现,但单次剂量600mg/kg,或从接种后24小时开始给予五剂300mg/kg,脓疱损伤数量可显著减少。在接受治疗的家兔中未观察到ara-A的毒性作用。