tetano
Editor, Senior Moderator
Curr Pathobiol Rep
. 2021 Dec 8;1-13.
doi: 10.1007/s40139-021-00226-0. Online ahead of print.
Chemokine-Based Therapeutics for the Treatment of Inflammatory and Fibrotic Convergent Pathways in COVID-19
Dana R Julian[SUP] 1 2 [/SUP], Megan A Kazakoff[SUP] 1 2 [/SUP], Akhil Patel[SUP] 1 [/SUP], Jesse Jaynes[SUP] 3 [/SUP], Monte S Willis[SUP] 4 5 [/SUP], Cecelia C Yates[SUP] 1 2 6 [/SUP]
Affiliations
Abstract
Coronavirus disease 2019 (COVID-19) is an infectious disease caused by the SARS-CoV-2 betacoronavirus and has taken over 761,426 American lives as of the date of publication and will likely result in long-term, if not permanent, tissue damage for countless patients. COVID-19 presents with diverse and multisystemic pathologic processes, including a hyperinflammatory response, acute respiratory distress syndrome (ARDS), vascular injury, microangiopathy, tissue fibrosis, angiogenesis, and widespread thrombosis across multiple organs, including the lungs, heart, kidney, liver, and brain. C-X-C chemokines contribute to these pathologies by attracting inflammatory mediators, the disruption of endothelial cell integrity and function, and the initiation and propagation of the cytokine storm. Among these, CXCL10 is recognized as a critical contributor to the hyperinflammatory state and poor prognosis in COVID-19. CXCL10 is also known to regulate growth factor-induced fibrosis, and recent evidence suggests the CXCL10-CXCR3 signaling system may be vital in targeting convergent pro-inflammatory and pro-fibrotic pathways. This review will explore the mechanistic role of CXCL10 and related chemokines in fibrotic complications associated with COVID-19 and the potential of CXCL10-targeted therapeutics for early intervention and long-term treatment of COVID-19-induced fibrosis.
Keywords: COVID-19; CXCL10; Chemokines; Fibrosis.
. 2021 Dec 8;1-13.
doi: 10.1007/s40139-021-00226-0. Online ahead of print.
Chemokine-Based Therapeutics for the Treatment of Inflammatory and Fibrotic Convergent Pathways in COVID-19
Dana R Julian[SUP] 1 2 [/SUP], Megan A Kazakoff[SUP] 1 2 [/SUP], Akhil Patel[SUP] 1 [/SUP], Jesse Jaynes[SUP] 3 [/SUP], Monte S Willis[SUP] 4 5 [/SUP], Cecelia C Yates[SUP] 1 2 6 [/SUP]
Affiliations
- PMID: 34900402
- PMCID: PMC8651461
- DOI: 10.1007/s40139-021-00226-0
Abstract
Coronavirus disease 2019 (COVID-19) is an infectious disease caused by the SARS-CoV-2 betacoronavirus and has taken over 761,426 American lives as of the date of publication and will likely result in long-term, if not permanent, tissue damage for countless patients. COVID-19 presents with diverse and multisystemic pathologic processes, including a hyperinflammatory response, acute respiratory distress syndrome (ARDS), vascular injury, microangiopathy, tissue fibrosis, angiogenesis, and widespread thrombosis across multiple organs, including the lungs, heart, kidney, liver, and brain. C-X-C chemokines contribute to these pathologies by attracting inflammatory mediators, the disruption of endothelial cell integrity and function, and the initiation and propagation of the cytokine storm. Among these, CXCL10 is recognized as a critical contributor to the hyperinflammatory state and poor prognosis in COVID-19. CXCL10 is also known to regulate growth factor-induced fibrosis, and recent evidence suggests the CXCL10-CXCR3 signaling system may be vital in targeting convergent pro-inflammatory and pro-fibrotic pathways. This review will explore the mechanistic role of CXCL10 and related chemokines in fibrotic complications associated with COVID-19 and the potential of CXCL10-targeted therapeutics for early intervention and long-term treatment of COVID-19-induced fibrosis.
Keywords: COVID-19; CXCL10; Chemokines; Fibrosis.