“…maribavir, letermovir, brincidofovir) are studied in ongoing clinical trials (www.clinicaltrials.gov; Sellar and Peggs, 2012), this case report indicates the urgent need for the development and market availability of new anti-CMV drugs. Although additional data are required, there might be role for artesunate in the treatment of mild CMV disease due to multidrug-resistant CMV strains (Germi et al, 2014).…”
“…maribavir, letermovir, brincidofovir) are studied in ongoing clinical trials (www.clinicaltrials.gov; Sellar and Peggs, 2012), this case report indicates the urgent need for the development and market availability of new anti-CMV drugs. Although additional data are required, there might be role for artesunate in the treatment of mild CMV disease due to multidrug-resistant CMV strains (Germi et al, 2014).…”
“…Cell cycle modulation via cyclin-dependent kinases and retinoblastoma protein appears to play an important role in artemisinins activities [56]. Unfortunately, there is not yet a thorough evaluation of its efficacy but only sporadic reports of its in vivo anti CMV activity with contrasting results [57]. Interesting insights come from artemisinin-derived dimers, novel compounds with more potent in vitro anti-CMV effects [58,59] the efficacy of which remains to be addressed.…”
“…In general, UL54 mutations emerge after prolonged GCV exposure and thereby increase the level of GCV resistance conferred by mutations already present in the UL97 gene (6)(7)(8)(9). Infections with multidrug-resistant CMV isolates that contain several mutations in the UL97 and/or UL54 genes were reported in immunocompromised patients (10)(11)(12). Such CMV infections may be associated with a single isolate that harbors multiple mutations in the UL97 and/or UL54 genes or may result from mixed virus subpopulations that harbor different mutations (6).…”
bCytomegalovirus resistance to antivirals is a major problem in transplant recipients. We evaluated the impact of five mutations (A594V, L595F, and E655K in the UL97 gene and V526L and E756K in the UL54 gene), detected in a blood sample from a stem cell transplant recipient, on drug susceptibilities and replicative capacities of recombinant viruses.
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