Management strategies for herpesvirus infections of the CNS - Immunocompetent and immunocompromised patients

Citation
P. Cinque et A. Lazzarin, Management strategies for herpesvirus infections of the CNS - Immunocompetent and immunocompromised patients, CNS DRUGS, 14(2), 2000, pp. 95-113
Citations number
153
Categorie Soggetti
Pharmacology,"Neurosciences & Behavoir
Journal title
CNS DRUGS
ISSN journal
11727047 → ACNP
Volume
14
Issue
2
Year of publication
2000
Pages
95 - 113
Database
ISI
SICI code
1172-7047(200008)14:2<95:MSFHIO>2.0.ZU;2-A
Abstract
The known human herpesviruses (HHVs) include herpes simplex viruses type 1 and 2, varicella-zoster virus, cytomegalovirus, Epstein-Barr virus, and HHV s 6, 7 and 8, Almost all of them may induce CNS diseases, which can vary fr om mild to life threatening and are significantly different in immunocompet ent and immunocompromised patients. An aetiological diagnosis is essential for optimal disease management, and the recently developed molecular diagno stic techniques have provided a rapid and sensitive means for herpesvirus i dentification. Effective antiherpesvirus agents have long been available, but the only reg imen that can be recommended on the basis of proven efficacy in controlled trials is aciclovir (acyclovir) for herpes simplex encephalitis (HSE). Neve rtheless, antiviral agents are empirically used in the treatment of various herpes-induced CNS complications and a number of examples of their efficac y have been reported. Most frequently, CNS disease results from direct viru s-induced cytotoxicity. However, immune-mediated mechanisms may be involved in some cases, and cortisosteroids are also empirically employed. Despite the diagnostic advances and broader availability of antiviral compo unds, the management of herpes-induced CNS complications is still difficult . A significant number of patients with HSE die, fail to regain normal func tion or relapse despite an initial therapeutic response. The current antivi ral approaches are often unsatisfactory in immunocompromised patients and n o optimal treatment has yet been established for the majority of herpes dis eases of the CNS. Information regarding new treatment strategies, including different aciclovir regimens and the use of newer compounds or drug combin ations, is needed and can only be provided by large multicentre studies.