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How we treat cytomegalovirus in hematopoietic cell transplant recipients.我们如何治疗造血细胞移植受者的巨细胞病毒感染。
Blood. 2009 Jun 4;113(23):5711-9. doi: 10.1182/blood-2008-10-143560. Epub 2009 Mar 18.
2
Anti-HIV drugs for cancer therapeutics: back to the future?用于癌症治疗的抗HIV药物:回归未来?
Lancet Oncol. 2009 Jan;10(1):61-71. doi: 10.1016/S1470-2045(08)70334-6.
3
Activation of Akt through gp130 receptor signaling is required for Kaposi's sarcoma-associated herpesvirus-induced lymphatic reprogramming of endothelial cells.通过gp130受体信号激活Akt是卡波西肉瘤相关疱疹病毒诱导内皮细胞淋巴管重编程所必需的。
J Virol. 2008 Sep;82(17):8771-9. doi: 10.1128/JVI.00766-08. Epub 2008 Jun 25.
4
Valganciclovir for suppression of human herpesvirus-8 replication: a randomized, double-blind, placebo-controlled, crossover trial.缬更昔洛韦抑制人疱疹病毒8型复制的随机、双盲、安慰剂对照、交叉试验。
J Infect Dis. 2008 Jul 1;198(1):23-30. doi: 10.1086/588820.
5
Persistent Kaposi sarcoma in the era of highly active antiretroviral therapy: characterizing the predictors of clinical response.高效抗逆转录病毒治疗时代的持续性卡波西肉瘤:确定临床反应的预测因素
AIDS. 2008 May 11;22(8):937-45. doi: 10.1097/QAD.0b013e3282ff6275.
6
Nelfinavir, A lead HIV protease inhibitor, is a broad-spectrum, anticancer agent that induces endoplasmic reticulum stress, autophagy, and apoptosis in vitro and in vivo.奈非那韦是一种主要的HIV蛋白酶抑制剂,是一种广谱抗癌剂,在体外和体内均可诱导内质网应激、自噬和凋亡。
Clin Cancer Res. 2007 Sep 1;13(17):5183-94. doi: 10.1158/1078-0432.CCR-07-0161.
7
NFV, an HIV-1 protease inhibitor, induces growth arrest, reduced Akt signalling, apoptosis and docetaxel sensitisation in NSCLC cell lines.NFV是一种HIV-1蛋白酶抑制剂,可诱导非小细胞肺癌细胞系生长停滞、Akt信号传导减弱、细胞凋亡并增强多西他赛敏感性。
Br J Cancer. 2006 Dec 18;95(12):1653-62. doi: 10.1038/sj.bjc.6603435. Epub 2006 Nov 28.
8
HIV protease inhibitors decrease VEGF/HIF-1alpha expression and angiogenesis in glioblastoma cells.HIV蛋白酶抑制剂可降低胶质母细胞瘤细胞中VEGF/HIF-1α的表达及血管生成。
Neoplasia. 2006 Nov;8(11):889-95. doi: 10.1593/neo.06535.
9
Double-stranded RNA binding by a heterodimeric complex of murine cytomegalovirus m142 and m143 proteins.鼠巨细胞病毒m142和m143蛋白异二聚体复合物对双链RNA的结合
J Virol. 2006 Oct;80(20):10173-80. doi: 10.1128/JVI.00905-06.
10
Nelfinavir induces liposarcoma apoptosis and cell cycle arrest by upregulating sterol regulatory element binding protein-1.奈非那韦通过上调固醇调节元件结合蛋白-1诱导脂肪肉瘤细胞凋亡和细胞周期停滞。
Anticancer Drugs. 2006 Sep;17(8):891-903. doi: 10.1097/01.cad.0000224448.08706.76.

HIV 蛋白酶抑制剂奈非那韦可抑制体外 Kaposi 肉瘤相关疱疹病毒的复制。

The HIV protease inhibitor nelfinavir inhibits Kaposi's sarcoma-associated herpesvirus replication in vitro.

机构信息

Department of Pediatrics, University of Washington, Seattle, Washington, USA.

出版信息

Antimicrob Agents Chemother. 2011 Jun;55(6):2696-703. doi: 10.1128/AAC.01295-10. Epub 2011 Mar 14.

DOI:10.1128/AAC.01295-10
PMID:21402841
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3101462/
Abstract

Kaposi's sarcoma (KS) is the most common HIV-associated cancer worldwide and is associated with high levels of morbidity and mortality in some regions. Antiretroviral (ARV) combination regimens have had mixed results for KS progression and resolution. Anecdotal case reports suggest that protease inhibitors (PIs) may have effects against KS that are independent of their effect on HIV infection. As such, we evaluated whether PIs or other ARVs directly inhibit replication of Kaposi's sarcoma-associated herpesvirus (KSHV), the gammaherpesvirus that causes KS. Among a broad panel of ARVs tested, only the PI nelfinavir consistently displayed potent inhibitory activity against KSHV in vitro as demonstrated by an efficient quantitative assay for infectious KSHV using a recombinant virus, rKSHV.294, which expresses the secreted alkaline phosphatase. This inhibitory activity of nelfinavir against KSHV replication was confirmed using virus derived from a second primary effusion lymphoma cell line. Nelfinavir was similarly found to inhibit in vitro replication of an alphaherpesvirus (herpes simplex virus) and a betaherpesvirus (human cytomegalovirus). No activity was observed with nelfinavir against vaccinia virus or adenovirus. Nelfinavir may provide unique benefits for the prevention or treatment of HIV-associated KS and potentially other human herpesviruses by direct inhibition of replication.

摘要

卡波西肉瘤(KS)是全球最常见的与 HIV 相关的癌症,在某些地区与高发病率和死亡率相关。抗逆转录病毒(ARV)联合治疗方案对 KS 的进展和消退的效果不一。一些偶然的病例报告表明,蛋白酶抑制剂(PI)可能对 KS 具有独立于其对 HIV 感染的作用的效果。因此,我们评估了 PI 或其他 ARV 是否直接抑制引起 KS 的卡波西肉瘤相关疱疹病毒(KSHV)的复制。在所测试的广泛 ARV 中,只有 PI 奈非那韦在体外一致显示出对 KSHV 的强大抑制活性,这通过使用表达分泌型碱性磷酸酶的重组病毒 rKSHV.294 的高效定量传染性 KSHV 测定得到证实。奈非那韦对 KSHV 复制的这种抑制活性在源自第二个原发性渗出性淋巴瘤细胞系的病毒中得到了确认。奈非那韦也被发现抑制体外复制的α疱疹病毒(单纯疱疹病毒)和β疱疹病毒(人巨细胞病毒)。奈非那韦对牛痘病毒或腺病毒没有活性。奈非那韦通过直接抑制复制,可能为预防或治疗 HIV 相关 KS 以及其他潜在的人类疱疹病毒提供独特的益处。