II. Mechanism
- Viruses lack the easy targets of Antibiotics (e.g. cell membranes, peptidoglycan cell walls, ribosomes)
-
Viruses have only a few potential targets for Antivirals
- Viral capsid (Protein coat)
- Nucleic Acids
- Enzymes for replication
- Most Antivirals target replication steps
- Results in virustatic agents that suppress replication, but do not kill the virus
- Viable virus remains in latent state
- Most common Antiviral mechanism is as Nucleotide analogues
- Act as non-functional decoys competitively binding viral replication enzymes
- Some are incorporated into DNA, resulting in non-functional enzyme Proteins
III. Medications: Herpesvirus Antivirals - Nucleic Acid Polymerase Inhibitors (DNA or RNA)
- See Herpesviridae
- See Herpes Simplex Virus (HSV)
- See Varicella Zoster Virus (VZV)
- See Cytomegalovirus (CMV)
- Synthetic Nucleoside analogues (e.g. Acyclovir, Famciclovir, Valacyclovir, Ganciclovir)
- Acyclovir, Famciclovir, Valacyclovir are indicated for Varicella Zoster Virus and Herpes Simplex Virus Infections
- Ganciclovir and Valgancyclovir have greater activity against CMV and EBV (used in AIDS and BMT patients)
- Agents are prodrugs metabolized by multiple enzymes (esp. thymidine kinase) to active triphosphate drug
- These prodrugs require thymidine kinase for actvity
- Famciclovir and Valacyclovir reach higher drug levels after oral ingestion than Acyclovir
- Famciclovir and Valacyclovir lack the protential nephrotoxicity of IV Acyclovir
- Thymidine kinase phosphorylates these prodrugs into their active form
- Thymidine kinase is found in Herpesviridae, but not in humans
- Acyclovir, Famciclovir and Valacyclovir are only active only when Herpes viruses are present
- Some strains of CMV do not carry Thymidine kinase
- Results in Antiviral resistance
- Thymidine kinase is found in Herpesviridae, but not in humans
- Pyrophosphate analog - DNA Polymerase Inhibitor (e.g. Foscarnet)
- Foscarnet is a synthetic analog of inorganic pyrophosphate
- Selectively blocks viral DNA Polymerases at their pyrophosphate binding site, preventing DNA Replication
- Indicated in CMV Retinitis and HSV infection in Immunocompromised patients
- Phosphonate Nucleoside analog - DNA Polymerase Inhibitor (e.g. Cidofovir)
- Active against the Herpes Family of Viruses, especially Cytomegalovirus (CMV).
- Synthetic, acyclic, monophosphate Nucleotide analog of deoxycytidine (deoxyribonucleoside in DNA synthesis)
- Cidofovir is activated within infected host cells, via phosphorylation by pyruvate kinases to Cidofovir diphosphate
- Cidofovir diphosphate competes with deoxycytosine-5-triphosphate (dCTP) for viral DNA Polymerase
- When incorporated into DNA, it prevents viral DNA polymerization, blocking viral DNA Replication
IV. Medications: HIV Antiviral Agents
- See Anti-Retroviral Therapy
- See HIV Pathophysiology
- Host Cell fusion and penetration inhibitors
- Fusion Inhibitors (e.g. Enfuvirtide)
- Blocks HIV fusion to cell anchor Proteins
- CCR5 Inhibitors (Maraviroc)
- Block HIV binding at CCR5 co-receptor
- CD4 Coreceptors (CCR5 or CXCR4) must be present on the host cell surface for HIV penetration
- Fusion Inhibitors (e.g. Enfuvirtide)
- Nucleic Acid Polymerase Inhibitors (DNA or RNA)
- Protease Inhibitors (e.g. Atazanavir, Darunavir, Fosamprenavir, Indinavir, Ritonavir, Saquinavir)
- Integrase Inhibitors (e.g. Bictegravir, Cabotegravir, Dolutegravir, Raltegravir)
V. Medications: Other Antiviral Agents
- Additional Antivirals are targeted at the infected host cell factors
-
Nucleic Acid Polymerase Inhibitors (DNA or RNA)
- NS5B Polymerase Inhibitors (e.g. Sofosbuvir) or NS5A Inhibitors (e.g. Velpatasvir)
- RdRP polymerase Inhibitor (e.g. Remdesivir)
- Protease Inhibitors (e.g. Atazanavir, Darunavir, Fosamprenavir, Indinavir, Ritonavir, Saquinavir)
-
Neuraminidase Inhibitor (e.g. Oseltamivir)
- Influenza Infection