Author: Egilmezer, Ece; Rawlinson, William D
Title: Review of studies of severe acute respiratory syndrome related coronavirus–2 pathogenesis in human organoid models Cord-id: 8f3kumw0 Document date: 2021_3_25
ID: 8f3kumw0
Snippet: Severe acute respiratory syndrome related coronavirusâ€2 (SARSâ€CoVâ€2) is the cause of Covidâ€19 which was classified as a global pandemic in March 2020. The increasing global health and economic burden of SARSâ€CoVâ€2 has necessitated urgent investigations into the pathogenesis of disease and development of therapeutic and vaccination regimens. Human trials of vaccine and antiviral candidates have been undertaken, but basic pathogenetic studies are still required to inform these trials.
Document: Severe acute respiratory syndrome related coronavirusâ€2 (SARSâ€CoVâ€2) is the cause of Covidâ€19 which was classified as a global pandemic in March 2020. The increasing global health and economic burden of SARSâ€CoVâ€2 has necessitated urgent investigations into the pathogenesis of disease and development of therapeutic and vaccination regimens. Human trials of vaccine and antiviral candidates have been undertaken, but basic pathogenetic studies are still required to inform these trials. Gaps in understanding of cellular infection by, and immunity to, SARSâ€CoVâ€2 mean additional models are required to assist in improved design of these therapeutics. Human organoids are threeâ€dimensional models that contain multiple cell types and mimic human organs in ex vivo culture conditions. The SARSâ€CoVâ€2 virus has been implicated in causing not only respiratory injury but also injury to other organs such as the brain, liver and kidneys. Consequently, a variety of different organoid models have been employed to investigate the pathogenic mechanisms of disease due to SARSâ€CoVâ€2. Data on these models have not been systematically assembled. In this review, we highlight key findings from studies that have utilised different human organoid types to investigate the expression of SARSâ€CoVâ€2 receptors, permissiveness, immune response, dysregulation of cellular functions, and potential antiviral therapeutics.
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