Health Problems

Ribavirin Mechanism

Ribavirin is a broad-spectrum antiviral nucleoside that is currently used in combination with interferon-alpha to treat hepatitis C virus infection, but is also employed as a monotherapy to treat severe cases of respiratory syncytial virus infection and Lassa fever virus infection.

The mechanism of action of ribavirin has been studied for decades. Shortly after the discovery in 1972, it was suggested that the antiviral activity of this drug is achieved is through inhibition of the cellular protein inosine monophosphate dehydrogenase (IMPDH).

Further studies have suggested that the antiviral activity of ribavirin may be related to its ability to inhibit capping of viral transcripts, to inhibit viral polymerase or to suppress cellular and humoral immune responses. In recent years it is considered that ribavirin’s primary antiviral mechanism is lethal mutagenesis of the viral RNA genomes.

Polymerase inhibition

As ribavirin is a nucleoside analogue of guanosine, the simplest mechanism would be to act as an inhibitor of the viral polymerase. And indeed, the direct inhibition of viral polymerases has been shown in vesicular stomatitis virus, La Crosse encephalitis virus, reovirus, influenza virus and hepatitis C virus.

Since viral polymerases use intracellular nucleotides in order to replicate their genome, ribavirin triphosphate is potentially recognized by the viral polymerase. Subsequent elongation is then inhibited due to chain termination or prevention of the binding of other endogenous nucleotides essential for the completion of genome replication.

Arguments against this mechanism of action are weak inhibition of hepatitis C virus polymerase and sustained antiviral activity against most strains with mutations in the polymerase region. That is the reason why co-administration of interferon-α is obligatory in the treatment of hepatitis C.

Lethal mutagenesis

An additional strategy of ribavirin is lethal mutagenesis, also termed “error catastrophe” in recognition of its conceptual origins. It consists in achieving large reductions of viral load and (in ideal cases) virus extinction by increasing the mutation rate of the virus over the critical error rate.

This mechanism of action would not select for a particularly resistant strain, as mutations would occur randomly throughout the genome. Evidence for this mechanism is controversial, as certain laboratories have published conflicting studies on the number of mutations generating during exposure to ribavirin.

Still, this mechanism is consistent with the fact that various RNA viruses exist as highly heterogeneous “quasispecies” due to high mutation frequency. This is often considered an evolutionary advantage, but results in a viral population close to the edge of "error catastrophe" –  i.e. a small increase in the error rate leads to a drastic loss of genome viability and infectivity.

Other mechanisms

As it was already mentioned, ribavirin can specifically bind to the substrate-binding site of the IMPDH enzyme, limiting access of the enzyme to its endogenous substrate (inosine-5-monophosphate), which ultimately leads to the decreased levels of intracellular guanosine triphosphate (GTP) pools required for viral replication.

More recently, different research groups have suggested that ribavirin may serve an immunomodulatory role, particularly on adaptive immune responses. It can act as an inducer of the helper-T-cell type 1 (Th1) cytokine response, but also as a suppressor of the type 2 (Th2) cytokine phenotype.

Ribavirin is also thought to have certain antitumor activity via inhibition of eIF4E, which is the rate-limiting component of the translation initiation complex. That has been associated with decreased protein levels of several eIF4E targets, such as cyclin D1 and NBS1. Consequently, some researchers are evaluating the efficacy of ribavirin in the setting of advanced breast cancer.

Sources

  1. http://www.cancerci.com/content/14/1/63
  2. http://www.liai.org/files/Ribavirin-Crotty.pdf
  3. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3682505/
  4. http://www.sciencedirect.com/science/article/pii/S0042682203001521
  5. www.researchgate.net/…/54461cee0cf22b3c14de06c2.pdf

Further Reading

  • All Ribavirin Content
  • Ribavirin – What is Ribavirin?
  • Ribavirin Marketing
  • Ribavirin History
  • Ribavirin Chemistry
More…

Last Updated: Aug 23, 2018

Written by

Dr. Tomislav Meštrović

Dr. Tomislav Meštrović is a medical doctor (MD) with a Ph.D. in biomedical and health sciences, specialist in the field of clinical microbiology, and an Assistant Professor at Croatia's youngest university – University North. In addition to his interest in clinical, research and lecturing activities, his immense passion for medical writing and scientific communication goes back to his student days. He enjoys contributing back to the community. In his spare time, Tomislav is a movie buff and an avid traveler.

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