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Elucidation of the liver pathophysiology of COVID-19 patients using liver-on-a-chips

Authors :
00422410
60546993
80523993
10759509
Deguchi, Sayaka
Kosugi, Kaori
Hashimoto, Rina
Sakamoto, Ayaka
Yamamoto, Masaki
Krol, Rafal P
Gee, Peter
Negoro, Ryosuke
Noda, Takeshi
Yamamoto, Takuya
Torisawa, Yu-suke
Nagao, Miki
Takayama, Kazuo
00422410
60546993
80523993
10759509
Deguchi, Sayaka
Kosugi, Kaori
Hashimoto, Rina
Sakamoto, Ayaka
Yamamoto, Masaki
Krol, Rafal P
Gee, Peter
Negoro, Ryosuke
Noda, Takeshi
Yamamoto, Takuya
Torisawa, Yu-suke
Nagao, Miki
Takayama, Kazuo
Publication Year :
2023

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.

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1458643898
Document Type :
Electronic Resource