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Copyright: ©Author(s) 2026. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution-NonCommercial (CC BY-NC 4.0) license. No commercial re-use. See permissions. Published by Baishideng Publishing Group Inc.
World J Hepatol. May 27, 2026; 18(5): 116542
Published online May 27, 2026. doi: 10.4254/wjh.v18.i5.116542
Liver injury after COVID-19 vaccination: Current status and future perspectives
Ken Sato
Ken Sato, Department of Healthcare Informatics, Takasaki University of Health and Welfare, Takasaki 370-0033, Japan
Author contributions: Sato K designed the overall concept and contributed to the writing, editing, and revision of the manuscript, illustrations, and literature review.
Conflict-of-interest statement: All the authors report no relevant conflicts of interest for this article.
Corresponding author: Ken Sato, MD, PhD, Professor, Department of Healthcare Informatics, Takasaki University of Health and Welfare, 37-1 Nakaorui-machi, Takasaki 370-0033, Japan. satoken@gunma-u.ac.jp
Received: November 17, 2025
Revised: January 18, 2026
Accepted: March 12, 2026
Published online: May 27, 2026
Processing time: 191 Days and 19.1 Hours
Core Tip

Core Tip: Liver injury following coronavirus disease 2019 vaccination presents with heterogeneous phenotypes, including new-onset autoimmune hepatitis, drug-induced autoimmune-like hepatitis, drug-induced liver injury, and secondary hepatic manifestations linked to comorbidities such as hemophagocytic lymphohistiocytosis. Vaccine-type differences in liver injury remain inconclusive. Prognosis varies by etiology; although many cases resolve spontaneously or respond to immunosuppressive therapy, some progress to acute liver failure necessitating transplantation or resulting in death. Vaccine rechallenge may not be contraindicated, but switching vaccine platforms is advised. The pathogenesis likely involves multifactorial mechanisms, such as genetic predispositions and immunological cross-reactivity between viral-specific antigens and host self-proteins.

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