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Serological response and breakthrough infection after COVID-19 vaccination in patients with cirrhosis and post-liver transplant

  • the COBALT Consortium
  • University College London
  • Foundation for Liver Research
  • Royal Free London NHS Foundation Trust
  • King's College London
  • Hospital Clinico Universitario de Valencia
  • European Foundation for the Study of Chronic Liver Failure (EF-CLIF)
  • Hospital Universitario La Fe
  • University of Valencia
  • Niguarda Hospital
  • University of Milan
  • Universidad Autónoma de Madrid
  • University Hospital La Paz
  • CIBERehd
  • University of Pavia
  • Vall D'Hebron Hospital
  • Leiden University
  • University of Padua
  • University of Udine
  • Azienda Ospedaiera Universitaria Integrata Verona
  • IRCCS Fondazione Ca'Granda – Ospedale Maggiore Policlinico - Milano
  • Hospital Universitario Virgen del Rocio
  • Research Institute of Sant Pau Hospital (IIB Sant Pau)
  • EUI-Sant Pau School of Nursing
  • Hospital Ramon y Cajal
  • University of Alcalá
  • King's College Hospital NHS Foundation Trust
  • University of Rome La Sapienza
  • University of Bologna

Research output: Contribution to journalArticlepeer-review

Abstract

Background: Vaccine hesitancy and lack of access remain major issues in disseminating COVID-19 vaccination to liver patients globally. Factors predicting poor response to vaccination and risk of breakthrough infection are important data to target booster vaccine programs. The primary aim of the current study was to measure humoral responses to 2 doses of COVID-19 vaccine. Secondary aims included the determination of factors predicting breakthrough infection. Methods: COVID-19 vaccination and Biomarkers in cirrhosis And post-Liver Transplantation is a prospective, multicenter, observational case-control study. Participants were recruited at 4-10 weeks following first and second vaccine doses in cirrhosis [n = 325; 94% messenger RNA (mRNA) and 6% viral vaccine], autoimmune liver disease (AILD) (n = 120; 77% mRNA and 23% viral vaccine), post-liver transplant (LT) (n = 146; 96% mRNA and 3% viral vaccine), and healthy controls (n = 51; 72% mRNA, 24% viral and 4% heterologous combination). Serological end points were measured, and data regarding breakthrough SARS-CoV-2 infection were collected. Results: After adjusting by age, sex, and time of sample collection, anti-Spike IgG levels were the lowest in post-LT patients compared to cirrhosis (p < 0.0001), AILD (p < 0.0001), and control (p = 0.002). Factors predicting reduced responses included older age, Child-Turcotte-Pugh B/C, and elevated IL-6 in cirrhosis; non-mRNA vaccine in AILD; and coronary artery disease, use of mycophenolate and dysregulated B-call activating factor, and lymphotoxin-α levels in LT. Incident infection occurred in 6.6%, 10.6%, 7.4%, and 15.6% of cirrhosis, AILD, post-LT, and control, respectively. The only independent factor predicting infection in cirrhosis was low albumin level. Conclusions: LT patients present the lowest response to the SARS-CoV-2 vaccine. In cirrhosis, the reduced response is associated with older age, stage of liver disease and systemic inflammation, and breakthrough infection with low albumin level.

Original languageEnglish
Pages (from-to)e0273
JournalHepatology Communications
Volume7
Issue number11
DOIs
Publication statusPublished - Nov 2023
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

ASJC Scopus subject areas

  • Hepatology

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