Rationale of using the dual chemokine receptor CCR2/CCR5 inhibitor cenicriviroc for the treatment of COVID-19.

Coronavirus Disease 2019 (COVID-19), caused by Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), has created a global pandemic infecting over 230 million people and costing millions of lives. Therapies to attenuate severe disease are desperately needed. Cenicriviroc (CVC), a C-C chemokin...

Full description

Bibliographic Details
Main Authors: Daniel Clark Files, Frank Tacke, Alexandra O'Sullivan, Patrick Dorr, William G Ferguson, William G Powderly
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2022-06-01
Series:PLoS Pathogens
Online Access:https://doi.org/10.1371/journal.ppat.1010547
_version_ 1828403103496404992
author Daniel Clark Files
Frank Tacke
Alexandra O'Sullivan
Patrick Dorr
William G Ferguson
William G Powderly
author_facet Daniel Clark Files
Frank Tacke
Alexandra O'Sullivan
Patrick Dorr
William G Ferguson
William G Powderly
author_sort Daniel Clark Files
collection DOAJ
description Coronavirus Disease 2019 (COVID-19), caused by Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), has created a global pandemic infecting over 230 million people and costing millions of lives. Therapies to attenuate severe disease are desperately needed. Cenicriviroc (CVC), a C-C chemokine receptor type 5 (CCR5) and C-C chemokine receptor type 2 (CCR2) antagonist, an agent previously studied in advanced clinical trials for patients with HIV or nonalcoholic steatohepatitis (NASH), may have the potential to reduce respiratory and cardiovascular organ failures related to COVID-19. Inhibiting the CCR2 and CCR5 pathways could attenuate or prevent inflammation or fibrosis in both early and late stages of the disease and improve outcomes of COVID-19. Clinical trials using CVC either in addition to standard of care (SoC; e.g., dexamethasone) or in combination with other investigational agents in patients with COVID-19 are currently ongoing. These trials intend to leverage the anti-inflammatory actions of CVC for ameliorating the clinical course of COVID-19 and prevent complications. This article reviews the literature surrounding the CCR2 and CCR5 pathways, their proposed role in COVID-19, and the potential role of CVC to improve outcomes.
first_indexed 2024-12-10T10:13:25Z
format Article
id doaj.art-1a96f9a38e594553b94d882c91ae3000
institution Directory Open Access Journal
issn 1553-7366
1553-7374
language English
last_indexed 2024-12-10T10:13:25Z
publishDate 2022-06-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS Pathogens
spelling doaj.art-1a96f9a38e594553b94d882c91ae30002022-12-22T01:53:04ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742022-06-01186e101054710.1371/journal.ppat.1010547Rationale of using the dual chemokine receptor CCR2/CCR5 inhibitor cenicriviroc for the treatment of COVID-19.Daniel Clark FilesFrank TackeAlexandra O'SullivanPatrick DorrWilliam G FergusonWilliam G PowderlyCoronavirus Disease 2019 (COVID-19), caused by Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), has created a global pandemic infecting over 230 million people and costing millions of lives. Therapies to attenuate severe disease are desperately needed. Cenicriviroc (CVC), a C-C chemokine receptor type 5 (CCR5) and C-C chemokine receptor type 2 (CCR2) antagonist, an agent previously studied in advanced clinical trials for patients with HIV or nonalcoholic steatohepatitis (NASH), may have the potential to reduce respiratory and cardiovascular organ failures related to COVID-19. Inhibiting the CCR2 and CCR5 pathways could attenuate or prevent inflammation or fibrosis in both early and late stages of the disease and improve outcomes of COVID-19. Clinical trials using CVC either in addition to standard of care (SoC; e.g., dexamethasone) or in combination with other investigational agents in patients with COVID-19 are currently ongoing. These trials intend to leverage the anti-inflammatory actions of CVC for ameliorating the clinical course of COVID-19 and prevent complications. This article reviews the literature surrounding the CCR2 and CCR5 pathways, their proposed role in COVID-19, and the potential role of CVC to improve outcomes.https://doi.org/10.1371/journal.ppat.1010547
spellingShingle Daniel Clark Files
Frank Tacke
Alexandra O'Sullivan
Patrick Dorr
William G Ferguson
William G Powderly
Rationale of using the dual chemokine receptor CCR2/CCR5 inhibitor cenicriviroc for the treatment of COVID-19.
PLoS Pathogens
title Rationale of using the dual chemokine receptor CCR2/CCR5 inhibitor cenicriviroc for the treatment of COVID-19.
title_full Rationale of using the dual chemokine receptor CCR2/CCR5 inhibitor cenicriviroc for the treatment of COVID-19.
title_fullStr Rationale of using the dual chemokine receptor CCR2/CCR5 inhibitor cenicriviroc for the treatment of COVID-19.
title_full_unstemmed Rationale of using the dual chemokine receptor CCR2/CCR5 inhibitor cenicriviroc for the treatment of COVID-19.
title_short Rationale of using the dual chemokine receptor CCR2/CCR5 inhibitor cenicriviroc for the treatment of COVID-19.
title_sort rationale of using the dual chemokine receptor ccr2 ccr5 inhibitor cenicriviroc for the treatment of covid 19
url https://doi.org/10.1371/journal.ppat.1010547
work_keys_str_mv AT danielclarkfiles rationaleofusingthedualchemokinereceptorccr2ccr5inhibitorcenicrivirocforthetreatmentofcovid19
AT franktacke rationaleofusingthedualchemokinereceptorccr2ccr5inhibitorcenicrivirocforthetreatmentofcovid19
AT alexandraosullivan rationaleofusingthedualchemokinereceptorccr2ccr5inhibitorcenicrivirocforthetreatmentofcovid19
AT patrickdorr rationaleofusingthedualchemokinereceptorccr2ccr5inhibitorcenicrivirocforthetreatmentofcovid19
AT williamgferguson rationaleofusingthedualchemokinereceptorccr2ccr5inhibitorcenicrivirocforthetreatmentofcovid19
AT williamgpowderly rationaleofusingthedualchemokinereceptorccr2ccr5inhibitorcenicrivirocforthetreatmentofcovid19