Eizuru Yoshito
Center for Chronic Viral Diseases, Graduate School of Medical and Dental Sciences, Kagoshima University, Japan.
Uirusu. 2005 Jun;55(1):95-104. doi: 10.2222/jsv.55.95.
The long-term treatment of herpesvirus infections with current antivirals leads to the development of drug-resistant viruses. Because currently available antivirals finally target the viral DNA polymerase, mutant resistant to one drug often shows cross-resistance to other drugs. This evidence highlights the need for the development of new antivirals that have the different viral targets. Recently, high-through-put screening of large compound collections for inhibiting specific viral enzymes, or in vitro cell culture assay, has identified several new antivirals. These include the inhibitors of helicase/primase complex, terminase complex, portal protein and UL97 protein kinase. This review will focus on these new compounds that directly inhibit viral replication.
目前使用的抗病毒药物对疱疹病毒感染进行长期治疗会导致耐药病毒的产生。由于目前可用的抗病毒药物最终靶向病毒DNA聚合酶,对一种药物耐药的突变体通常对其他药物也表现出交叉耐药性。这一证据凸显了开发具有不同病毒靶点的新型抗病毒药物的必要性。最近,通过对大量化合物库进行高通量筛选以抑制特定病毒酶,或进行体外细胞培养测定,已经鉴定出几种新型抗病毒药物。这些药物包括解旋酶/引发酶复合物、末端酶复合物、门户蛋白和UL97蛋白激酶的抑制剂。本综述将聚焦于这些直接抑制病毒复制的新型化合物。