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新型抗疱疹病毒药物。其作用靶点与治疗潜力。

New antiherpesvirus agents. Their targets and therapeutic potential.

作者信息

Alrabiah F A, Sacks S L

机构信息

Department of Medicine, University of British Columbia, Vancouver, Canada.

出版信息

Drugs. 1996 Jul;52(1):17-32. doi: 10.2165/00003495-199652010-00002.

Abstract

Of the large number of agents under development for the treatment of herpes virus infections [herpes simplex virus types 1 and 2 (HSV-1 and HSV-2), varicella zoster virus (VZV), cytomegalovirus (CMV), Epstein-Barr virus (EBV)], only ten have apparently reached clinical development. Aciclovir was approved for the treatment of HSV infections over 10 years ago, and it remains an important and reliable antiviral agent. Recent approvals in some countries of valaciclovir for VZV infection and famciclovir for both HSV and VZV infections demonstrate the rapidity of change in this field. Intravenous ganciclovir and foscarnet are approved for the treatment of CMV infection in the immunocompromised patient. Five of the antiherpetic drugs under current clinical development are nucleoside analogues or their prodrugs; another is a phosphorylated nucleoside (nucleotide). Four of the nucleoside agents-penciclovir, famciclovir, valaciclovir and lobucavir-are being developed for the management of HSV and VZV infections. Valaciclovir is also being developed for the prevention of CMV infections and famciclovir and lobucavir for the treatment of hepatitis B virus infection. Oral ganciclovir, lobucavir, ISIS 2922 and cidofovir are being developed for the suppression of CMV infections in immunocompromised patients. Sorivudine has been studied in VZV infections. n-Docosanol is under development for HSV infections, and cidofovir is being developed for both HSV and CMV infections, as well as for treatment of other viral diseases. Traditionally, the adverse effects associated with anti-CMV compounds have been more difficult to manage and are acceptable clinically only because of the severity of the underlying infection and lack of safer therapeutic alternatives. In general, toxicity issues continue to be problematic in the anti-CMV arena, although newer agents have improved the situation to some extent. In contrast, the safety of anti-HSV compounds has traditionally been excellent, establishing a safety standard that must be met by newer agents entering the field.

摘要

在大量正在研发用于治疗疱疹病毒感染的药物中(单纯疱疹病毒1型和2型、水痘带状疱疹病毒、巨细胞病毒、爱泼斯坦-巴尔病毒),只有10种药物显然已进入临床研发阶段。阿昔洛韦在10多年前就被批准用于治疗单纯疱疹病毒感染,至今仍是一种重要且可靠的抗病毒药物。近期一些国家批准伐昔洛韦用于水痘带状疱疹病毒感染,泛昔洛韦用于单纯疱疹病毒和水痘带状疱疹病毒感染,这表明该领域变化迅速。静脉用更昔洛韦和膦甲酸钠被批准用于治疗免疫功能低下患者的巨细胞病毒感染。目前正在进行临床研发的抗疱疹药物中有5种是核苷类似物或其前体药物;另一种是磷酸化核苷(核苷酸)。4种核苷类药物——喷昔洛韦、泛昔洛韦、伐昔洛韦和洛布卡韦——正在研发用于治疗单纯疱疹病毒和水痘带状疱疹病毒感染。伐昔洛韦也在研发用于预防巨细胞病毒感染,泛昔洛韦和洛布卡韦用于治疗乙型肝炎病毒感染。口服更昔洛韦、洛布卡韦、ISIS 2922和西多福韦正在研发用于抑制免疫功能低下患者的巨细胞病毒感染。索立夫定已在水痘带状疱疹病毒感染中进行了研究。正二十二醇正在研发用于单纯疱疹病毒感染,西多福韦正在研发用于单纯疱疹病毒和巨细胞病毒感染,以及治疗其他病毒性疾病。传统上,与抗巨细胞病毒化合物相关的不良反应更难处理,仅因为潜在感染的严重性和缺乏更安全的治疗选择才在临床上被接受。总体而言,尽管新型药物在一定程度上改善了这种情况,但毒性问题在抗巨细胞病毒领域仍然存在问题。相比之下,抗单纯疱疹病毒化合物的安全性传统上一直很好,为进入该领域的新型药物确立了必须达到的安全标准。

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