Hepatitis B reactivation: A possible cause of coronavirus disease 2019 vaccine induced hepatitis

Background and aims: Coronavirus disease 2019 (COVID-19) vaccines were rapidly implemented globally and vaccine-associated immune-related hepatitis was recently reported. We aim to investigate its impact in regions endemic of chronic hepatitis B (CHB). Methods: We retrospectively collected patients...

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Main Authors: Hsin-Yun Wu, Tung-Hung Su, Chun-Jen Liu, Hung-Chih Yang, Jia-Huei Tsai, Ming-Han Wei, Chieh-Chang Chen, Chien-Chih Tung, Jia-Horng Kao, Pei-Jer Chen
Format: Article
Language:English
Published: Elsevier 2024-01-01
Series:Journal of the Formosan Medical Association
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0929664623002358
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author Hsin-Yun Wu
Tung-Hung Su
Chun-Jen Liu
Hung-Chih Yang
Jia-Huei Tsai
Ming-Han Wei
Chieh-Chang Chen
Chien-Chih Tung
Jia-Horng Kao
Pei-Jer Chen
author_facet Hsin-Yun Wu
Tung-Hung Su
Chun-Jen Liu
Hung-Chih Yang
Jia-Huei Tsai
Ming-Han Wei
Chieh-Chang Chen
Chien-Chih Tung
Jia-Horng Kao
Pei-Jer Chen
author_sort Hsin-Yun Wu
collection DOAJ
description Background and aims: Coronavirus disease 2019 (COVID-19) vaccines were rapidly implemented globally and vaccine-associated immune-related hepatitis was recently reported. We aim to investigate its impact in regions endemic of chronic hepatitis B (CHB). Methods: We retrospectively collected patients who developed hepatitis within 90 days after COVID-19 vaccination in Taiwan. The mechanisms of hepatitis included vaccine induced liver injury (VILI) and immune-related hepatitis, which are direct liver injuries defined as aspartate or alanine aminotransferase (AST or ALT) increased ≥ 5-fold upper limit of normal (ULN) and/or AST or ALT ≥ 3-fold of ULN with concurrent total bilirubin ≥ 2-fold of ULN. Indirect liver injury due to HBV reactivation was defined as HBsAg reverse seroconversion or significant rise in HBV DNA level. The demographics, clinical data, and course of hepatitis were compared statistically. Results: Twenty-five patients were included with a median age of 54. The culprit vaccines were ChAdOx1 nCoV-19 (n = 9), mRNA-1273 (n = 12), and BNT162b2 (n = 4). The characteristics of hepatitis were comparable regardless of vaccine subtypes. The median onset of hepatitis was 25 days post vaccination, with a peak of 10-fold ALT-increase. The etiologies included HBV reactivation (n = 10), VILI (n = 10), and immune-related hepatitis (n = 5). HBV reactivation accounts for 90% of vaccine-induced hepatitis in patients of CHB (n = 10), and two patients died. Patients with initial AST levels >500 U/L increased 27-fold risks of liver injury greater than moderate severity compared with those without. Conclusion: COVID-19 vaccine induced hepatitis is a clinical significant complication, and HBV reactivation may account for a possible mechanism.
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spelling doaj.art-d9660f192670472da0db06e0aabeb2a22024-01-23T04:14:56ZengElsevierJournal of the Formosan Medical Association0929-66462024-01-0112318897Hepatitis B reactivation: A possible cause of coronavirus disease 2019 vaccine induced hepatitisHsin-Yun Wu0Tung-Hung Su1Chun-Jen Liu2Hung-Chih Yang3Jia-Huei Tsai4Ming-Han Wei5Chieh-Chang Chen6Chien-Chih Tung7Jia-Horng Kao8Pei-Jer Chen9Division of Gastroenterology and Hepatology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, TaiwanDivision of Gastroenterology and Hepatology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan; Hepatitis Research Center, National Taiwan University Hospital, Taipei, Taiwan; Corresponding author. Division of Gastroenterology and Hepatology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan 1 Chang-Te Street, Taipei 10048, Taiwan.Division of Gastroenterology and Hepatology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan; Hepatitis Research Center, National Taiwan University Hospital, Taipei, TaiwanDivision of Gastroenterology and Hepatology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, TaiwanDepartment of Pathology, National Taiwan University Hospital, Taipei, TaiwanDivision of Gastroenterology, Department of Internal Medicine, National Taiwan University Hospital Hsin-Chu Branch, BioMedical Park Hospital, HsinChu, TaiwanDivision of Gastroenterology and Hepatology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, TaiwanDivision of Gastroenterology and Hepatology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, TaiwanDivision of Gastroenterology and Hepatology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan; Hepatitis Research Center, National Taiwan University Hospital, Taipei, TaiwanDivision of Gastroenterology and Hepatology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan; Hepatitis Research Center, National Taiwan University Hospital, Taipei, Taiwan; Corresponding author. Graduate Institute of Clinical Medicine, College of Medicine, National Taiwan University, 1 Chang-Te Street, Taipei 10048, Taiwan.Background and aims: Coronavirus disease 2019 (COVID-19) vaccines were rapidly implemented globally and vaccine-associated immune-related hepatitis was recently reported. We aim to investigate its impact in regions endemic of chronic hepatitis B (CHB). Methods: We retrospectively collected patients who developed hepatitis within 90 days after COVID-19 vaccination in Taiwan. The mechanisms of hepatitis included vaccine induced liver injury (VILI) and immune-related hepatitis, which are direct liver injuries defined as aspartate or alanine aminotransferase (AST or ALT) increased ≥ 5-fold upper limit of normal (ULN) and/or AST or ALT ≥ 3-fold of ULN with concurrent total bilirubin ≥ 2-fold of ULN. Indirect liver injury due to HBV reactivation was defined as HBsAg reverse seroconversion or significant rise in HBV DNA level. The demographics, clinical data, and course of hepatitis were compared statistically. Results: Twenty-five patients were included with a median age of 54. The culprit vaccines were ChAdOx1 nCoV-19 (n = 9), mRNA-1273 (n = 12), and BNT162b2 (n = 4). The characteristics of hepatitis were comparable regardless of vaccine subtypes. The median onset of hepatitis was 25 days post vaccination, with a peak of 10-fold ALT-increase. The etiologies included HBV reactivation (n = 10), VILI (n = 10), and immune-related hepatitis (n = 5). HBV reactivation accounts for 90% of vaccine-induced hepatitis in patients of CHB (n = 10), and two patients died. Patients with initial AST levels >500 U/L increased 27-fold risks of liver injury greater than moderate severity compared with those without. Conclusion: COVID-19 vaccine induced hepatitis is a clinical significant complication, and HBV reactivation may account for a possible mechanism.http://www.sciencedirect.com/science/article/pii/S0929664623002358Autoimmune hepatitisDrug induced liver injuryHepatitis BSARS-CoV-2Vaccination
spellingShingle Hsin-Yun Wu
Tung-Hung Su
Chun-Jen Liu
Hung-Chih Yang
Jia-Huei Tsai
Ming-Han Wei
Chieh-Chang Chen
Chien-Chih Tung
Jia-Horng Kao
Pei-Jer Chen
Hepatitis B reactivation: A possible cause of coronavirus disease 2019 vaccine induced hepatitis
Journal of the Formosan Medical Association
Autoimmune hepatitis
Drug induced liver injury
Hepatitis B
SARS-CoV-2
Vaccination
title Hepatitis B reactivation: A possible cause of coronavirus disease 2019 vaccine induced hepatitis
title_full Hepatitis B reactivation: A possible cause of coronavirus disease 2019 vaccine induced hepatitis
title_fullStr Hepatitis B reactivation: A possible cause of coronavirus disease 2019 vaccine induced hepatitis
title_full_unstemmed Hepatitis B reactivation: A possible cause of coronavirus disease 2019 vaccine induced hepatitis
title_short Hepatitis B reactivation: A possible cause of coronavirus disease 2019 vaccine induced hepatitis
title_sort hepatitis b reactivation a possible cause of coronavirus disease 2019 vaccine induced hepatitis
topic Autoimmune hepatitis
Drug induced liver injury
Hepatitis B
SARS-CoV-2
Vaccination
url http://www.sciencedirect.com/science/article/pii/S0929664623002358
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