Antiviral treatment of cytomegalovirus infection: an update

被引:36
作者
Haerter, Georg [2 ]
Michel, Detlef [1 ]
机构
[1] Univ Ulm Klinikum, Inst Virol, D-89081 Ulm, Germany
[2] Univ Ulm Klinikum, Sekt Infektiol & Klin Immunol, Innere Med Klin 3, D-89081 Ulm, Germany
关键词
antiviral treatment; cytomegalovirus; ganciclovir; resistance; virus evolution; RESISTANT CYTOMEGALOVIRUS; TRANSPLANT RECIPIENTS; GANCICLOVIR; MUTATIONS; DISEASE; UL97; PROPHYLAXIS; ARTESUNATE; MARIBAVIR;
D O I
10.1517/14656566.2012.658775
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
This editorial summarizes recent developments in the management of ganciclovir-resistant human cytomegalovirus (HCMV) infections. All current drugs available for systemic treatment, including ganciclovir (GCV), valganciclovir, foscarnet and cidofovir, target the viral polymerase. However, all such compounds are hampered by dose-related toxicities and the emergence of resistance. Different approaches (e. g., PCR-based direct sequencing, pyrosequencing, mass spectrometry-based comparative sequencing) allow the fast detection of resistant HCMV and are well suited to therapy monitoring. However, more studies are required on the dynamic of mixed HCMV populations under drug pressure. Alternate antiviral compounds with new mechanisms of action, such as artesunate, leflunomid, letermovir and maribavir, are now being investigated in clinical studies. An advantage of some of the new substances is lesser toxicity issues, which might lead to new prophylactic and treatment strategies.
引用
收藏
页码:623 / 627
页数:5
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