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dc.contributor.author | Deguchi, Sayaka | en |
dc.contributor.author | Kosugi, Kaori | en |
dc.contributor.author | Hashimoto, Rina | en |
dc.contributor.author | Sakamoto, Ayaka | en |
dc.contributor.author | Yamamoto, Masaki | en |
dc.contributor.author | Krol, Rafal P | en |
dc.contributor.author | Gee, Peter | en |
dc.contributor.author | Negoro, Ryosuke | en |
dc.contributor.author | Noda, Takeshi | en |
dc.contributor.author | Yamamoto, Takuya | en |
dc.contributor.author | Torisawa, Yu-suke | en |
dc.contributor.author | Nagao, Miki | en |
dc.contributor.author | Takayama, Kazuo | en |
dc.contributor.alternative | 出口, 清香 | ja |
dc.contributor.alternative | 小杉, 佳織 | ja |
dc.contributor.alternative | 橋本, 里菜 | ja |
dc.contributor.alternative | 坂本, 綾香 | ja |
dc.contributor.alternative | 山本, 正樹 | ja |
dc.contributor.alternative | 根来, 亮介 | ja |
dc.contributor.alternative | 野田, 岳志 | ja |
dc.contributor.alternative | 山本, 拓也 | ja |
dc.contributor.alternative | 鳥澤, 勇介 | ja |
dc.contributor.alternative | 長尾, 美紀 | ja |
dc.contributor.alternative | 高山, 和雄 | ja |
dc.date.accessioned | 2023-03-09T06:46:41Z | - |
dc.date.available | 2023-03-09T06:46:41Z | - |
dc.date.issued | 2023-03 | - |
dc.identifier.uri | http://hdl.handle.net/2433/279615 | - |
dc.description | 新型コロナウイルス感染症(COVID-19)研究のための肝臓チップの開発 --肝障害の病態解明と治療薬の評価--. 京都大学プレスリリース. 2023-03-08. | ja |
dc.description | Using organ-on-a-chip technology to elucidate the liver pathophysiology of COVID-19 patients. 京都大学プレスリリース. 2023-03-08. | en |
dc.description.abstract | SARS-CoV-2 induces severe organ damage not only in the lung but also in the liver, heart, kidney, and intestine. It is known that COVID-19 severity correlates with liver dysfunction, but few studies have investigated the liver pathophysiology in COVID-19 patients. Here, we elucidated liver pathophysiology in COVID-19 patients using organs-on-a-chip technology and clinical analyses. First, we developed liver-on-a-chip (LoC) which recapitulating hepatic functions around the intrahepatic bile duct and blood vessel. We found that hepatic dysfunctions, but not hepatobiliary diseases, were strongly induced by SARS-CoV-2 infection. Next, we evaluated the therapeutic effects of COVID-19 drugs to inhibit viral replication and recover hepatic dysfunctions, and found that the combination of anti-viral and immunosuppressive drugs (Remdesivir and Baricitinib) is effective to treat hepatic dysfunctions caused by SARS-CoV-2 infection. Finally, we analyzed the sera obtained from COVID-19 patients, and revealed that COVID-19 patients, who were positive for serum viral RNA, are likely to become severe and develop hepatic dysfunctions, as compared with COVID-19 patients who were negative for serum viral RNA. We succeeded in modeling the liver pathophysiology of COVID-19 patients using LoC technology and clinical samples. | en |
dc.language.iso | eng | - |
dc.publisher | Oxford University Press (OUP) | en |
dc.rights | © The Author(s) 2023. Published by Oxford University Press on behalf of National Academy of Sciences. | en |
dc.rights | This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. | en |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | - |
dc.subject | SARS-CoV-2 | en |
dc.subject | COVID-19 | en |
dc.subject | organs-on-a-chip | en |
dc.subject | liver-on-a-chip | en |
dc.subject | Remdesivir | en |
dc.subject | Baricitinib | en |
dc.title | Elucidation of the liver pathophysiology of COVID-19 patients using liver-on-a-chips | en |
dc.type | journal article | - |
dc.type.niitype | Journal Article | - |
dc.identifier.jtitle | PNAS Nexus | en |
dc.identifier.volume | 2 | - |
dc.identifier.issue | 3 | - |
dc.relation.doi | 10.1093/pnasnexus/pgad029 | - |
dc.textversion | publisher | - |
dc.identifier.artnum | pgad029 | - |
dc.address | Center for iPS Cell Research and Application (CiRA), Kyoto University; Department of Medical Science, Graduate School of Medicine, Kyoto University | en |
dc.address | Center for iPS Cell Research and Application (CiRA), Kyoto University | en |
dc.address | Center for iPS Cell Research and Application (CiRA), Kyoto University | en |
dc.address | Center for iPS Cell Research and Application (CiRA), Kyoto University | en |
dc.address | Department of Clinical Laboratory Medicine, Graduate School of Medicine, Kyoto University | en |
dc.address | CiRA Foundation, Research and Development Center | en |
dc.address | MaxCyte, Inc. | en |
dc.address | Laboratory of Molecular Pharmacokinetics, College of Pharmaceutical Sciences, Ritsumeikan University | en |
dc.address | Laboratory of Ultrastructural Virology, Institute for Frontier Life and Medical Sciences, Kyoto University; CREST, Japan Science and Technology Agency (JST) | en |
dc.address | Center for iPS Cell Research and Application (CiRA), Kyoto University; Institute for the Advanced Study of Human Biology (WPI-ASHBi), Kyoto University; Medical-risk Avoidance based on iPS Cells Team, RIKEN Center for Advanced Intelligence Project (AIP) | en |
dc.address | Department of Micro Engineering, Kyoto University | en |
dc.address | Department of Clinical Laboratory Medicine, Graduate School of Medicine, Kyoto University | en |
dc.address | Center for iPS Cell Research and Application (CiRA), Kyoto University; AMED-CREST, Japan Agency for Medical Research and Development (AMED) | en |
dc.identifier.pmid | 36896132 | - |
dcterms.accessRights | open access | - |
dc.identifier.eissn | 2752-6542 | - |
出現コレクション: | 学術雑誌掲載論文等 |

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