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安普那韦对人免疫缺陷病毒感染的原代巨噬细胞具有强大的抗病毒活性。

Potent antiviral activity of amprenavir in primary macrophages infected by human immunodeficiency virus.

作者信息

Aquaro Stefano, Guenci Tania, Di Santo Fabiola, Francesconi Mauro, Caliò Raffaele, Perno Carlo Federico

机构信息

Department of Experimental Medicine and Biochemical Sciences, University of Rome Tor Vergata, Via Montpellie 1, Rome 00133, Italy.

出版信息

Antiviral Res. 2004 Feb;61(2):133-7. doi: 10.1016/j.antiviral.2003.09.002.

Abstract

Objective of the present study was then to assess the antiviral activity of the protease inhibitor amprenavir in macrophages (M/M), and to compare it with its efficacy in peripheral blood lymphocytes (PBL). M/M were obtained from blood of sero-negative healthy donors and infected with M-tropic HIV-1 strain (HIV-1(Ba-L)). The stabilized infection was assessed by monitoring the HIV-1 p24 gag antigen production in the supernatants of M/M cultures. In the setting of acute infection (treatment before HIV-1 challenge), amprenavir showed substantial activity both in M/M and PBL at similar concentrations (EC(50): 0.011 and 0.031 microM, respectively); complete inhibition of HIV-1 replication was achieved in both cell types at concentration of about 2 microM. In the setting of chronical infection (i.e. antiviral treatment several days after established infection), an antiviral effect of amprenavir was achieved in M/M, but at concentrations higher than those active in acutely infected M/M (EC(50): 0.72 microM, EC(90): 18.2 microM). The antiviral effect in chronically infected M/M was sustained for at least 2 weeks of continuous treatment. These findings suggest that amprenavir (at relatively high concentrations) has a clinically relevant antiviral effect in persistently infected reservoirs of HIV.

摘要

本研究的目的是评估蛋白酶抑制剂安普那韦在巨噬细胞(M/M)中的抗病毒活性,并将其与在外周血淋巴细胞(PBL)中的疗效进行比较。M/M取自血清阴性健康供者的血液,并感染了M嗜性HIV-1株(HIV-1(Ba-L))。通过监测M/M培养上清液中HIV-1 p24 gag抗原的产生来评估稳定感染情况。在急性感染情况下(HIV-1攻击前治疗),安普那韦在M/M和PBL中以相似浓度均表现出显著活性(EC(50)分别为0.011和0.031 microM);在约2 microM的浓度下,两种细胞类型中HIV-1复制均被完全抑制。在慢性感染情况下(即感染确立数天后进行抗病毒治疗),安普那韦在M/M中产生了抗病毒作用,但所需浓度高于急性感染M/M中的活性浓度(EC(50):0.72 microM,EC(90):18.2 microM)。在慢性感染的M/M中,抗病毒作用在持续治疗至少2周的时间内得以维持。这些发现表明,安普那韦(在相对较高浓度下)在HIV持续感染的储存库中具有临床相关的抗病毒作用。

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