Treatment of alpha and beta herpesvirus infections in solid organ transplant recipients

被引:5
作者
Abad, C. L. [1 ,2 ]
Razonable, R. R. [1 ,3 ]
机构
[1] Mayo Clin, Dept Med, Div Infect Dis, Rochester, MN USA
[2] Univ Philippines, Infect Dis Sect, Dept Med, Philippine Gen Hosp, Manila, Philippines
[3] Mayo Clin, William J Von Liebig Ctr Transplantat & Clin Rege, Rochester, MN USA
关键词
Herpesvirus; infection; solid organ transplant; VARICELLA-ZOSTER-VIRUS; GANCICLOVIR-RESISTANT CYTOMEGALOVIRUS; REPLICATION IN-VITRO; INTEGRATED HUMAN HERPESVIRUS-6; HUMAN-IMMUNODEFICIENCY-VIRUS; DOSE ORAL ACYCLOVIR; EXTENDED VALGANCICLOVIR PROPHYLAXIS; HEMATOPOIETIC-CELL TRANSPLANTATION; ACYCLIC NUCLEOSIDE PHOSPHONATES; POLYOMAVIRUS BK REPLICATION;
D O I
10.1080/14787210.2017.1266253
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Introduction: Human herpesviruses frequently cause infections in solid organ transplant (SOT) recipients.Areas covered: We provide an overview of the clinical impact of alpha and beta herpesviruses and highlight the mechanisms of action, pharmacokinetics, clinical indications, and adverse effects of antiviral drugs for the management of herpes simplex virus, varicella zoster virus and cytomegalovirus. We comprehensively evaluated key clinical trials that led to drug approval, and served as the foundation for management guidelines. We further provide an update on investigational antiviral agents for alpha and beta herpesvirus infections after SOT.Expert commentary: The therapeutic armamentarium for herpes infections is limited by the emergence of drug resistance. There have been major efforts for discovery of new drugs against these viruses, but the results of early-phase clinical trials have been less than encouraging. We believe, however, that more antiviral drug options are needed given the adverse side effects associated with current antiviral agents, and the emergence of drug-resistant virus populations in SOT recipients. Likewise, optimized use and strategies are needed for existing and novel antiviral drugs against alpha and beta-herpesviruses in SOT recipients.
引用
收藏
页码:93 / 110
页数:18
相关论文
共 202 条
[1]   INHIBITING EFFECT OF (RS)-9-[4-HYDROXY-2-(HYDROXYMETHYL)BUTYL] GUANINE ON VARICELLA-ZOSTER VIRUS-REPLICATION IN CELL-CULTURE [J].
ABELE, G ;
KARLSTROM, A ;
HARMENBERG, J ;
SHIGETA, S ;
LARSSON, A ;
LINDBORG, B ;
WAHREN, B .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1987, 31 (01) :76-80
[2]   Valacyclovir [J].
Acosta, EP ;
Fletcher, CV .
ANNALS OF PHARMACOTHERAPY, 1997, 31 (02) :185-191
[3]   Herpes zoster infection after liver transplantation in patients receiving induction therapy with alemtuzumab [J].
Alcaide, Maria L. ;
Abbo, Lilian ;
Pano, Jose R. ;
Gaynor, Jeffrey J. ;
Tryphonopoulos, Panagiotis ;
Weppler, Debbie ;
Moon, Jang I. ;
Tzakis, Andreas G. ;
Morris, Michele I. .
CLINICAL TRANSPLANTATION, 2008, 22 (04) :502-507
[4]   Increased antiviral activity of 1-O-hexadecyloxypropyl-[ 2-14C] cidofovir in MRC-5 human lung fibroblasts is explained by unique cellular uptake and metabolism [J].
Aldern, KA ;
Ciesla, SL ;
Winegarden, KL ;
Hostetler, KY .
MOLECULAR PHARMACOLOGY, 2003, 63 (03) :678-681
[5]   Anterior uveitis associated with intravenous cidofovir use in patients with cytomegalovirus retinitis [J].
Ambati, J ;
Wynne, KB ;
Angerame, MC ;
Robinson, MR .
BRITISH JOURNAL OF OPHTHALMOLOGY, 1999, 83 (10) :1153-1158
[6]  
[Anonymous], 2007, DRUGS R D, V8, P188
[7]   Human herpesvirus 7 primary infection in kidney transplant recipients [J].
Anton, Andres ;
Cervera, Carlos ;
Pumarola, Tomas ;
Moreno, Asuncion ;
Benito, Natividad ;
Linares, Laura ;
Esteva, Cristina ;
Cofan, Federico ;
de Anta, Maria Teresa Jimenez ;
Marcos, Maria Angeles .
TRANSPLANTATION, 2008, 85 (02) :298-302
[8]  
Arazi HC, 1999, TRANSPLANT P, V31, P2530
[9]   Varicella zoster virus-associated disease in adult kidney transplant recipients: incidence and risk-factor analysis [J].
Arness, T. ;
Pedersen, R. ;
Dierkhising, R. ;
Kremers, W. ;
Patel, R. .
TRANSPLANT INFECTIOUS DISEASE, 2008, 10 (04) :260-268
[10]  
Arvin A, 2007, HUMAN HERPESVIRUSES: BIOLOGY, THERAPY, AND IMMUNOPROPHYLAXIS, P1, DOI 10.2277/ 0521827140