The chemokine receptor antagonist cenicriviroc inhibits the replication of SARS-CoV-2 in vitro

Antiviral Res. 2020 Oct:182:104902. doi: 10.1016/j.antiviral.2020.104902. Epub 2020 Jul 30.


Cenicriviroc (CVC) is a small-molecule chemokine receptor antagonist with highly potent and selective anti-human immunodeficiency virus type 1 (HIV-1) activity through antagonizing C-C chemokine receptor type 5 (CCR5) as a coreceptor of HIV-1. CVC also strongly antagonizes C-C chemokine receptor type 2b (CCR2b), thereby it has potent anti-inflammatory and immunomodulatory effects. CVC is currently under clinical trials in the patients for treatment of nonalcoholic steatohepatitis, in which immune cell activation and dysregulation of proinflammatory cytokines play an important role in its pathogenesis. In this study, CVC was examined for its inhibitory effect on the replication of SARS-CoV-2, the causative agent of COVID-19, in cell cultures and found to be a selective inhibitor of the virus. The 50% effective concentrations of CVC were 19.0 and 2.9 μM in the assays based on the inhibition of virus-induced cell destruction and viral RNA levels in culture supernatants of the infected cells, respectively. Interestingly, the CCR5-specific antagonist maraviroc did not show any anti-SARS-CoV-2 activity. Although the mechanism of SARS-CoV-2 inhibition by CVC remains to be elucidated, CCR2b does not seem to be its target molecule. Considering the fact that the regulation of excessive immune activation is required to treat COVID-19 patients at the late stage of the disease, CVC should be further pursued for its potential in the treatment of SARS-CoV-2 infection.

Keywords: COVID-19; Cenicriviroc; Chemokine receptor antagonist; Cytokine storm; SARS-CoV-2.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antiviral Agents / pharmacology
  • Betacoronavirus / drug effects*
  • Betacoronavirus / physiology*
  • COVID-19
  • COVID-19 Drug Treatment
  • Chlorocebus aethiops
  • Coronavirus Infections / drug therapy*
  • Coronavirus Infections / virology*
  • Humans
  • Imidazoles / pharmacology*
  • Maraviroc / pharmacology
  • Pandemics
  • Pneumonia, Viral / drug therapy*
  • Pneumonia, Viral / virology*
  • Receptors, CCR2 / antagonists & inhibitors*
  • SARS-CoV-2
  • Sulfoxides
  • Vero Cells
  • Virus Replication / drug effects*


  • Antiviral Agents
  • Imidazoles
  • Receptors, CCR2
  • Sulfoxides
  • cenicriviroc
  • Maraviroc