Minireviews
Copyright ©The Author(s) 2021.
World J Stem Cells. May 26, 2021; 13(5): 439-451
Published online May 26, 2021. doi: 10.4252/wjsc.v13.i5.439
Table 1 Resume of organoid infection models developed for severe acute respiratory syndrome coronavirus 2 study
Ref.
Organoid infection model
Reported advantages
Yang et al[15]hPSC-derived cells/organoids, including pancreatic endocrine cells, liver organoids, endothelial cells, cardiomyocytes, macrophages, microglia, cortical neurons, and dopaminergic neuronsPermissiveness to SARS-CoV-2 infection; ACE2 expression was detected; Chemokine induction
Han et al[16]hPSC-LOshPSC-LOs (particularly alveolar type-II-like cells) are permissive to SARS-CoV-2 infection; Robust chemokine induction; Discovery and test therapeutic drugs
hPSC-COsPermissiveness to SARS-CoV-2 infection hPSC-Cos especially enterocytes, express ACE2; Discovery and test therapeutic drugs
Pei et al[18]hAWOs and hALOs from hESCsPermissiveness to SARS-CoV-2 infection and replication; Infected cells express ACE2 but not all ACE2 expressing cells were infected; Chemokine induction; Discovery and test therapeutic drugs
Yiangou et al[20]hPSC-derived cardiac modelsPermissiveness to SARS-CoV-2 infection; Activation of the innate inflammatory response; Show contractility, electrophysiology, and sarcomeric fragmentation
Monteil et al[22]Human capillary organoids from iPSCs; Kidney organoids from hESCsPermissiveness to SARS-CoV-2 infection and significantly inhibited by human recombinant soluble ACE2. ACE2 expression