Meta‐analysis of the immunogenicity of standard and booster SARS‐CoV‐2 vaccination in patients with chronic liver disease and post‐liver transplantation

Author:

Wang Wen‐Xin12,Wang Jitao3,Jia Rui4,Martini Silvia5,Liu Jiaye1,Huang Yifei6,Wang Fu‐Sheng12,Qi Xiaolong7ORCID,Fu Junliang12

Affiliation:

1. Senior Department of Infectious Diseases The Fifth Medical Center of Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases Beijing China

2. Peking University 302 Clinical Medical School Beijing China

3. CHESS‐COVID‐19 Group, Xingtai People's Hospital Xingtai Hebei China

4. Department of Gastroenterology The 985th Hospital of Joint Logistic Support Force of Chinese PLA Taiyuan Shanxi China

5. Neonatal Intensive Care Unit, AOU Bologna, Department of Medical and Surgical Sciences (DIMEC) University of Bologna Bologna Italy

6. CHESS Center, Institute of Portal Hypertension The First Hospital of Lanzhou University Lanzhou Gansu China

7. Center of Portal Hypertension, Department of Radiology, Zhongda Hospital, Medical School Southeast University Nanjing Jiangsu China

Abstract

AbstractAimsPatients with liver disease may exhibit higher infection rates and mortality rates from coronavirus disease 2019 (COVID‐19) than healthy individuals, and vaccination against severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) is an effective prevention strategy. This meta‐analysis aimed to assess the effectiveness and safety of SARS‐CoV‐2 vaccines in patients with chronic liver disease (CLD) and post‐liver transplantation (LT).MethodsThe PubMed, Embase, and Cochrane databases were searched. A random‐effects model meta‐analysis was used to determine the seropositivity rates of SARS‐CoV‐2 antibodies, odds ratio (OR) compared with healthy controls (HC), risk ratio (RR) between the booster and standard vaccination regimen, and the rate of adverse reactions (ADR).ResultsIn the standard vaccination regimen analysis, 17 controlled articles were included for effectiveness analysis, and six articles for ADR analysis. The pooled seropositivity rates of SARS‐CoV‐2 antibodies in patients with CLD and post‐LT were 93.3% (95% confidence interval [CI]: 89.0%–97.6%) and 69.1% (95% CI: 63.0%–75.3%), respectively. Both rates were lower than those in HC (p < 0.001). The differences remained significant after sorting by detection interval, vaccine type, antibody type, or CLD type. LT recipients showed much lower seropositivity rates of antibodies than patients with CLD (69.1% vs. 93.3%) or HC (OR: 0.055). The pooled total ADR rate of patients was 24.0% (95% CI: 16.2%–31.8%). In the booster vaccination regimen analysis, 11 prospective studies were enrolled, and the seropositivity rates of antibodies after the booster dose were increased by 27% compared with those of the standard vaccination regimen (RR: 1.27, 95% CI: 1.15–1.41, p < 0.001).ConclusionPatients with CLD and post‐LT can gain protection against COVID‐19 from standard vaccines, demonstrating a potentially weaker immunogenic response than HC. Booster vaccines can compensate for this deficiency. Therefore, patients with CLD and post‐LT should be prioritized for receiving the COVID‐19 booster vaccine.

Publisher

Wiley

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