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INTRODUCTION

The replication of viruses depends on synthetic processes of the host cell. Antiviral drugs can exert their actions at several stages of viral replication including viral entry, nucleic acid synthesis and integration, late protein synthesis, and processing, as well as in the final stages of viral packaging and virion release (Figure 49–1). Most of the drugs active against herpes simplex viruses (HSV) and many agents active against human immunodeficiency virus (HIV) are antimetabolites, structurally similar to naturally occurring compounds. The selective toxicity of antiviral drugs usually depends on greater susceptibility of viral enzymes to their inhibitory actions than host cell enzymes.

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One of the most important trends in viral chemotherapy, especially in the management of HIV infection, has been the introduction of combination drug therapy. This can result in greater clinical effectiveness in viral infections and can also prevent, or delay, the emergence of resistance.

FIGURE 49–1

The major sites of antiviral drug action. Note: interferon-α are speculated to have multiple sites of action on viral replication. (Reproduced with permission from Katzung BG, Vanderah TW: Basic & Clinical Pharmacology, 15th ed. New York, NY: McGraw Hill; 2021.)

ANTI-HERPES DRUGS

Most drugs active against herpes viruses are antimetabolites bioactivated via viral or host cell kinases to form compounds that inhibit viral DNA polymerases. Some of these agents are also used against cytomegalovirus (CMV).

A. Acyclovir (Acycloguanosine)

1. Mechanisms

Acyclovir is a guanosine analog active against herpes simplex virus (HSV-1, HSV-2) and varicella-zoster virus (VZV). The drug is activated initially by the viral kinase to form acyclovir triphosphate, which interferes with viral synthesis in two ways. It acts as a competitive substrate for DNA polymerase, and it leads to chain termination after its incorporation into viral DNA (Figure 49–2). Resistance of HSV can involve changes in viral DNA polymerase. However, many resistant strains of HSV (TK strains) lack thymidine kinase, the enzyme involved in the initial viral-specific phosphorylation of acyclovir. Such strains are cross-resistant to famciclovir, ganciclovir, and valacyclovir.

FIGURE 49–2

Mechanism of action of antiherpes agents. (Reproduced with permission from Katzung BG, Vanderah TW: Basic & Clinical Pharmacology, 15th ed. New York, NY: McGraw Hill; 2021.)

2. Pharmacokinetics

Acyclovir can be administered by the topical, oral, and intravenous routes. Because of its short half-life, oral administration requires multiple daily doses of acyclovir. Renal excretion is the major route of elimination of acyclovir, and dosage should be reduced in patients with renal impairment.

3. Clinical uses and toxicity

Oral acyclovir is commonly used for the treatment of mucocutaneous and genital herpes lesions (Table 49–1...

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