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      Herpes simplex virus resistance to acyclovir and penciclovir after two decades of antiviral therapy.

      Clinical microbiology reviews
      Acyclovir, analogs & derivatives, chemistry, therapeutic use, Antiviral Agents, Drug Resistance, Viral, Herpes Simplex, drug therapy, epidemiology, physiopathology, Humans, Microbial Sensitivity Tests, Simplexvirus, drug effects

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          Abstract

          Acyclovir, penciclovir, and their prodrugs have been widely used during the past two decades for the treatment of herpesvirus infections. In spite of the distribution of over 2.3 x 10(6) kg of these nucleoside analogues, the prevalence of acyclovir resistance in herpes simplex virus isolates from immunocompetent hosts has remained stable at approximately 0.3%. In immuncompromised patients, in whom the risk for developing resistance is much greater, the prevalence of resistant virus has also remained stable but at a higher level, typically 4 to 7%. These observations are examined in the light of characteristics of the virus, the drugs, and host factors.

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